| Year |
Citation |
Score |
| 2020 |
Krienen FM, Goldman M, Zhang Q, C H Del Rosario R, Florio M, Machold R, Saunders A, Levandowski K, Zaniewski H, Schuman B, Wu C, Lutservitz A, Mullally CD, Reed N, Bien E, ... ... Walsh CA, et al. Innovations present in the primate interneuron repertoire. Nature. PMID 32999462 DOI: 10.1038/s41586-020-2781-z |
0.38 |
|
| 2020 |
Shao DD, Achkar CM, Lai A, Srivastava S, Doan RN, Rodan LH, Chen AY, Poduri A, Yang E, Walsh CA. Polymicrogyria is associated with pathogenic variants in PTEN. Annals of Neurology. PMID 32959437 DOI: 10.1002/ana.25904 |
0.333 |
|
| 2020 |
Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, Hill RS, Chahrour MH, Mehta BK, Servattalab S, Ataman B, Lam AN, Morrow EM, Greenberg ME, Yu TW, Walsh CA, Markianos K. Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045. PMID 32820185 DOI: 10.1038/S41598-020-70656-0 |
0.815 |
|
| 2020 |
Kim J, Zhao B, Huang AY, Miller MB, Lodato MA, Walsh CA, Lee EA. APP gene copy number changes reflect exogenous contamination. Nature. 584: E20-E28. PMID 32814883 DOI: 10.1038/S41586-020-2522-3 |
0.776 |
|
| 2020 |
Lim ET, Uddin M, De Rubeis S, Chan Y, Kamumbu AS, Zhang X, D'Gama AM, Kim SN, Hill RS, Goldberg AP, Poultney C, Minshew NJ, Kushima I, Aleksic B, Ozaki N, ... ... Walsh CA, et al. Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience. PMID 32665711 DOI: 10.1038/S41593-020-0681-Z |
0.794 |
|
| 2020 |
Wang P, Shah GL, Landau HJ, Coulter ME, Walsh CA, Roider E, Kramer CS, Beuning PJ, Giese RW. Jettison-MS of Nucleic Acid Species. Journal of the American Society For Mass Spectrometry. PMID 32551641 DOI: 10.1021/Jasms.0C00084 |
0.682 |
|
| 2020 |
Huang AY, Li P, Rodin RE, Kim SN, Dou Y, Kenny CJ, Akula SK, Hodge RD, Bakken TE, Miller JA, Lein ES, Park PJ, Lee EA, Walsh CA. Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain. Proceedings of the National Academy of Sciences of the United States of America. PMID 32522880 DOI: 10.1073/Pnas.2006163117 |
0.787 |
|
| 2020 |
Dias CM, Walsh CA. Recent Advances in Understanding the Genetic Architecture of Autism. Annual Review of Genomics and Human Genetics. PMID 32396753 DOI: 10.1146/annurev-genom-121219-082309 |
0.353 |
|
| 2020 |
Khan A, Alaamery M, Massadeh S, Obaid A, Kashgari AA, Walsh CA, Eyaid W. PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly. Clinical Genetics. PMID 32286682 DOI: 10.1111/cge.13756 |
0.46 |
|
| 2020 |
Coulter ME, Musaev D, DeGennaro EM, Zhang X, Henke K, James KN, Smith RS, Hill RS, Partlow JN, Muna Al-Saffar, Kamumbu AS, Hatem N, Barkovich AJ, Aziza J, Chassaing N, ... ... Walsh CA, et al. Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32103185 DOI: 10.1038/S41436-020-0758-9 |
0.796 |
|
| 2020 |
Kodani A, Kenny C, Lai A, Gonzalez DM, Stronge E, Sejourne GM, Isacco L, Partlow JN, O'Donnell A, McWalter K, Byrne AB, Barkovich AJ, Yang E, Hill RS, Gawlinski P, ... ... Walsh CA, et al. Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5. Neuron. PMID 32097629 DOI: 10.1016/J.Neuron.2020.01.030 |
0.422 |
|
| 2020 |
Smith RS, Walsh CA. Ion Channel Functions in Early Brain Development. Trends in Neurosciences. PMID 31959360 DOI: 10.1016/j.tins.2019.12.004 |
0.477 |
|
| 2020 |
Dou Y, Kwon M, Rodin RE, Cortés-Ciriano I, Doan R, Luquette LJ, Galor A, Bohrson C, Walsh CA, Park PJ. Accurate detection of mosaic variants in sequencing data without matched controls. Nature Biotechnology. PMID 31907404 DOI: 10.1038/S41587-019-0368-8 |
0.384 |
|
| 2019 |
Lodato MA, Walsh CA. Corrigendum: Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms. Human Molecular Genetics. PMID 31778186 DOI: 10.1093/hmg/ddz286 |
0.72 |
|
| 2019 |
Dias CM, Punetha J, Zheng C, Mazaheri N, Rad A, Efthymiou S, Petersen A, Dehghani M, Pehlivan D, Partlow JN, Posey JE, Salpietro V, Gezdirici A, Malamiri RA, Al Menabawy NM, ... ... Walsh CA, et al. Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. American Journal of Human Genetics. PMID 31668703 DOI: 10.1016/J.Ajhg.2019.09.025 |
0.579 |
|
| 2019 |
Amrom D, Poduri A, Goldman JS, Dan B, Deconinck N, Pichon B, Nadaf J, Andermann F, Andermann E, Walsh CA, Dobyns WB. Duplication 2p16 is associated with perisylvian polymicrogyria. American Journal of Medical Genetics. Part A. PMID 31660690 DOI: 10.1002/ajmg.a.61342 |
0.393 |
|
| 2019 |
Lodato MA, Walsh CA. Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms. Human Molecular Genetics. PMID 31578549 DOI: 10.1093/Hmg/Ddz191 |
0.768 |
|
| 2019 |
Doan RN, Lim ET, De Rubeis S, Betancur C, Cutler DJ, Chiocchetti AG, Overman LM, Soucy A, Goetze S, Freitag CM, Daly MJ, Walsh CA, Buxbaum JD, Yu TW. Recessive gene disruptions in autism spectrum disorder. Nature Genetics. PMID 31209396 DOI: 10.1038/S41588-019-0433-8 |
0.673 |
|
| 2019 |
Kodani A, Moyer T, Chen A, Holland A, Walsh CA, Reiter JF. SFI1 promotes centriole duplication by recruiting USP9X to stabilize the microcephaly protein STIL. The Journal of Cell Biology. PMID 31197030 DOI: 10.1083/Jcb.201803041 |
0.407 |
|
| 2019 |
Ansar M, Ullah F, Paracha SA, Adams DJ, Lai A, Pais L, Iwaszkiewicz J, Millan F, Sarwar MT, Agha Z, Shah SF, Qaisar AA, Falconnet E, Zoete V, Ranza E, ... ... Walsh C, et al. Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features. American Journal of Human Genetics. PMID 31079899 DOI: 10.1016/j.ajhg.2019.04.002 |
0.401 |
|
| 2019 |
Bohrson CL, Barton AR, Lodato MA, Rodin RE, Luquette LJ, Viswanadham VV, Gulhan DC, Cortés-Ciriano I, Sherman MA, Kwon M, Coulter ME, Galor A, Walsh CA, Park PJ. Linked-read analysis identifies mutations in single-cell DNA-sequencing data. Nature Genetics. PMID 30886424 DOI: 10.1038/S41588-019-0366-2 |
0.814 |
|
| 2018 |
Khalil R, Kenny C, Hill RS, Mochida GH, Nasir R, Partlow JN, Barry BJ, Al-Saffar M, Egan C, Stevens CR, Gabriel SB, Barkovich AJ, Ellison JW, Al-Gazali L, Walsh CA, et al. PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30421579 DOI: 10.1002/ajmg.b.32688 |
0.734 |
|
| 2018 |
D'Gama AM, Walsh CA. Somatic mosaicism and neurodevelopmental disease. Nature Neuroscience. 21: 1504-1514. PMID 30349109 DOI: 10.1038/s41593-018-0257-3 |
0.761 |
|
| 2018 |
Rodin RE, Walsh CA. Somatic Mutation in Pediatric Neurological Diseases. Pediatric Neurology. PMID 30249355 DOI: 10.1016/j.pediatrneurol.2018.08.008 |
0.448 |
|
| 2018 |
Shaheen R, Maddirevula S, Ewida N, Alsahli S, Abdel-Salam GMH, Zaki MS, Tala SA, Alhashem A, Softah A, Al-Owain M, Alazami AM, Abadel B, Patel N, Al-Sheddi T, Alomar R, ... ... Walsh C, et al. Genomic and phenotypic delineation of congenital microcephaly. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30214071 DOI: 10.1038/S41436-018-0140-3 |
0.303 |
|
| 2018 |
Walsh CA. Rainer W. Guillery and the genetic analysis of brain development. The European Journal of Neuroscience. PMID 30152010 DOI: 10.1111/ejn.14135 |
0.366 |
|
| 2018 |
Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, ... ... Walsh CA, et al. Sodium Channel SCN3A (Na1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development. Neuron. PMID 30146301 DOI: 10.1016/J.Neuron.2018.07.052 |
0.806 |
|
| 2018 |
Coulter ME, Dorobantu CM, Lodewijk GA, Delalande F, Cianferani S, Ganesh VS, Smith RS, Lim ET, Xu CS, Pang S, Wong ET, Lidov HGW, Calicchio ML, Yang E, Gonzalez DM, ... ... Walsh CA, et al. The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Reports. 24: 973-986.e8. PMID 30044992 DOI: 10.1016/J.Celrep.2018.06.100 |
0.808 |
|
| 2018 |
Doan RN, Shin T, Walsh CA. Evolutionary Changes in Transcriptional Regulation: Insights into Human Behavior and Neurological Conditions. Annual Review of Neuroscience. 41: 185-206. PMID 29986162 DOI: 10.1146/annurev-neuro-080317-062104 |
0.348 |
|
| 2018 |
Bizzotto S, Walsh CA. Making a Notch in the Evolution of the Human Cortex. Developmental Cell. 45: 548-550. PMID 29870717 DOI: 10.1016/j.devcel.2018.05.015 |
0.314 |
|
| 2018 |
Jayaraman D, Bae BI, Walsh CA. The Genetics of Primary Microcephaly. Annual Review of Genomics and Human Genetics. PMID 29799801 DOI: 10.1146/annurev-genom-083117-021441 |
0.661 |
|
| 2018 |
Baizabal JM, Mistry M, García MT, Gómez N, Olukoya O, Tran D, Johnson MB, Walsh CA, Harwell CC. The Epigenetic State of PRDM16-Regulated Enhancers in Radial Glia Controls Cortical Neuron Position. Neuron. PMID 29779941 DOI: 10.1016/J.Neuron.2018.04.033 |
0.539 |
|
| 2018 |
Heinzen EL, O'Neill AC, Zhu X, Allen AS, Bahlo M, Chelly J, Dobyns WB, Freytag S, Guerrini R, Leventer RJ, Poduri A, Robertson SP, Walsh CA, Zhang M, et al. De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. Plos Genetics. 14: e1007281. PMID 29738522 DOI: 10.1371/journal.pgen.1007281 |
0.425 |
|
| 2018 |
Stouffs K, Stergachis AB, Vanderhasselt T, Dica A, Janssens S, Vandervore L, Gheldof A, Bodamer O, Keymolen K, Seneca S, Liebaers I, Jayaraman D, Hill HE, Partlow JN, Walsh CA, et al. Expanding the clinical spectrum of biallelic ZNF335 variants. Clinical Genetics. PMID 29652087 DOI: 10.1111/cge.13260 |
0.326 |
|
| 2018 |
Johnson MB, Sun X, Kodani A, Borges-Monroy R, Girskis KM, Ryu SC, Wang PP, Patel K, Gonzalez DM, Woo YM, Yan Z, Liang B, Smith RS, Chatterjee M, Coman D, ... ... Walsh CA, et al. Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size. Nature. PMID 29643508 DOI: 10.1038/S41586-018-0035-0 |
0.743 |
|
| 2017 |
D'Gama AM, Woodworth MB, Hossain AA, Bizzotto S, Hatem NE, LaCoursiere CM, Najm I, Ying Z, Yang E, Barkovich AJ, Kwiatkowski DJ, Vinters HV, Madsen JR, Mathern GW, Blümcke I, ... ... Walsh CA, et al. Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias. Cell Reports. 21: 3754-3766. PMID 29281825 DOI: 10.1016/J.Celrep.2017.11.106 |
0.828 |
|
| 2017 |
Lodato MA, Rodin RE, Bohrson CL, Coulter ME, Barton AR, Kwon M, Sherman MA, Vitzthum CM, Luquette LJ, Yandava C, Yang P, Chittenden TW, Hatem NE, Ryu SC, Woodworth MB, ... ... Walsh CA, et al. Aging and neurodegeneration are associated with increased mutations in single human neurons. Science (New York, N.Y.). PMID 29217584 DOI: 10.1126/Science.Aao4426 |
0.813 |
|
| 2017 |
Sherman MA, Barton AR, Lodato MA, Vitzthum C, Coulter ME, Walsh CA, Park PJ. PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation. Nucleic Acids Research. PMID 29186545 DOI: 10.1093/Nar/Gkx1195 |
0.784 |
|
| 2017 |
Marsh AP, Edwards TJ, Galea C, Cooper HM, Engle EC, Jamuar SS, Méneret A, Moutard ML, Nava C, Rastetter A, Robinson G, Rouleau G, Roze E, Spencer-Smith M, Trouillard O, ... ... Walsh CA, et al. DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum and developmental split brain syndrome. Human Mutation. PMID 29068161 DOI: 10.1002/Humu.23361 |
0.676 |
|
| 2017 |
Murray Sherman S, Mason CA, Atabay KD, Kaas JH, LaMantia AS, Mitchell A, Walsh C. Rainer (Ray) W. Guillery 28 August 1929-7 April 2017. The European Journal of Neuroscience. 46: 1933-1936. PMID 28782225 DOI: 10.1111/Ejn.13639 |
0.747 |
|
| 2017 |
Lim ET, Uddin M, De Rubeis S, Chan Y, Kamumbu AS, Zhang X, D'Gama AM, Kim SN, Hill RS, Goldberg AP, Poultney C, Minshew NJ, Kushima I, Aleksic B, Ozaki N, ... ... Walsh CA, et al. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience. PMID 28714951 DOI: 10.1038/Nn.4598 |
0.827 |
|
| 2017 |
Evrony GD, Cordero DR, Shen J, Partlow JN, Yu TW, Rodin RE, Hill RS, Coulter ME, Lam AN, Jayaraman D, Gerrelli D, Diaz DG, Santos C, Morrison V, Galli A, ... ... Walsh CA, et al. Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Genome Research. PMID 28630177 DOI: 10.1101/Gr.219899.116 |
0.826 |
|
| 2017 |
McConnell MJ, Moran JV, Abyzov A, Akbarian S, Bae T, Cortes-Ciriano I, Erwin JA, Fasching L, Flasch DA, Freed D, Ganz J, Jaffe AE, Kwan KY, Kwon M, Lodato MA, ... ... Walsh CA, et al. Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network. Science (New York, N.Y.). 356. PMID 28450582 DOI: 10.1126/Science.Aal1641 |
0.835 |
|
| 2017 |
Lakhani S, Doan R, Almureikhi M, Partlow JN, Al Saffar M, Elsaid MF, Alaaraj N, James Barkovich A, Walsh CA, Ben-Omran T. Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy. European Journal of Medical Genetics. PMID 28254648 DOI: 10.1016/j.ejmg.2017.02.006 |
0.426 |
|
| 2017 |
Jamuar SS, Schmitz-Abe K, D'Gama AM, Drottar M, Chan WM, Peeva M, Servattalab S, Lam AN, Delgado MR, Clegg NJ, Zayed ZA, Dogar MA, Alorainy IA, Jamea AA, Abu-Amero K, ... ... Walsh CA, et al. Biallelic mutations in human DCC cause developmental split-brain syndrome. Nature Genetics. PMID 28250456 DOI: 10.1038/Ng.3804 |
0.824 |
|
| 2017 |
Woodworth MB, Girskis KM, Walsh CA. Building a lineage from single cells: genetic techniques for cell lineage tracking. Nature Reviews. Genetics. PMID 28111472 DOI: 10.1038/nrg.2016.159 |
0.615 |
|
| 2016 |
Jayaraman D, Kodani A, Gonzalez DM, Mancias JD, Mochida GH, Vagnoni C, Johnson J, Krogan N, Harper JW, Reiter JF, Yu TW, Bae BI, Walsh CA. Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate. Neuron. 92: 813-828. PMID 27974163 DOI: 10.1016/J.Neuron.2016.09.056 |
0.797 |
|
| 2016 |
Johnson MB, Walsh CA. Cerebral cortical neuron diversity and development at single-cell resolution. Current Opinion in Neurobiology. 42: 9-16. PMID 27888678 DOI: 10.1016/j.conb.2016.11.001 |
0.543 |
|
| 2016 |
Ataman B, Boulting GL, Harmin DA, Yang MG, Baker-Salisbury M, Yap EL, Malik AN, Mei K, Rubin AA, Spiegel I, Durresi E, Sharma N, Hu LS, Pletikos M, Griffith EC, ... ... Walsh CA, et al. Evolution of Osteocrin as an activity-regulated factor in the primate brain. Nature. 539: 242-247. PMID 27830782 DOI: 10.1038/Nature20111 |
0.78 |
|
| 2016 |
Wang X, Zhang Z, Morris N, Cai T, Lee S, Wang C, Yu TW, Walsh CA, Lin X. Rare variant association test in family-based sequencing studies. Briefings in Bioinformatics. PMID 27677958 DOI: 10.1093/Bib/Bbw083 |
0.709 |
|
| 2016 |
Doan RN, Bae BI, Cubelos B, Chang C, Hossain AA, Al-Saad S, Mukaddes NM, Oner O, Al-Saffar M, Balkhy S, Gascon GG, Nieto M, Walsh CA. Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior. Cell. PMID 27667684 DOI: 10.1016/J.Cell.2016.08.071 |
0.779 |
|
| 2016 |
Zhang X, Chen MH, Wu X, Kodani A, Fan J, Doan R, Ozawa M, Ma J, Yoshida N, Reiter JF, Black DL, Kharchenko PV, Sharp PA, Walsh CA. Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex. Cell. 166: 1147-1162.e15. PMID 27565344 DOI: 10.1016/J.Cell.2016.07.025 |
0.77 |
|
| 2016 |
Evrony GD, Lee E, Park PJ, Walsh CA. Resolving rates of mutation in the brain using single-neuron genomics. Elife. 5. PMID 26901440 DOI: 10.7554/Elife.12966 |
0.799 |
|
| 2016 |
Oaks AW, Zamarbide M, Tambunan DE, Santini E, Di Costanzo S, Pond HL, Johnson MW, Lin J, Gonzalez DM, Boehler JF, Wu GK, Klann E, Walsh CA, Manzini MC. Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social Deficits. Cerebral Cortex (New York, N.Y. : 1991). PMID 26826102 DOI: 10.1093/Cercor/Bhw009 |
0.819 |
|
| 2016 |
Evrony GD, Lee E, Park PJ, Walsh CA. Author response: Resolving rates of mutation in the brain using single-neuron genomics Elife. DOI: 10.7554/Elife.12966.016 |
0.775 |
|
| 2015 |
D'Gama AM, Pochareddy S, Li M, Jamuar SS, Reiff RE, Lam AT, Sestan N, Walsh CA. Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms. Neuron. 88: 910-7. PMID 26637798 DOI: 10.1016/J.Neuron.2015.11.009 |
0.802 |
|
| 2015 |
Mutch CA, Poduri A, Sahin M, Barry B, Walsh CA, Barkovich AJ. Disorders of Microtubule Function in Neurons: Imaging Correlates. Ajnr. American Journal of Neuroradiology. PMID 26564436 DOI: 10.3174/Ajnr.A4552 |
0.797 |
|
| 2015 |
Al-Maawali A, Barry BJ, Rajab A, El-Quessny M, Seman A, Coury SN, Barkovich AJ, Yang E, Walsh CA, Mochida GH, Stoler JM. Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizures. American Journal of Medical Genetics. Part A. PMID 26463574 DOI: 10.1002/Ajmg.A.37422 |
0.41 |
|
| 2015 |
Lodato MA, Woodworth MB, Lee S, Evrony GD, Mehta BK, Karger A, Lee S, Chittenden TW, D'Gama AM, Cai X, Luquette LJ, Lee E, Park PJ, Walsh CA. Somatic mutation in single human neurons tracks developmental and transcriptional history. Science (New York, N.Y.). 350: 94-8. PMID 26430121 DOI: 10.1126/Science.Aab1785 |
0.827 |
|
| 2015 |
Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF, Klei L, Mandell JD, ... ... Walsh CA, et al. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 87: 1215-1233. PMID 26402605 DOI: 10.1016/J.Neuron.2015.09.016 |
0.799 |
|
| 2015 |
Kodani A, Yu TW, Johnson JR, Jayaraman D, Johnson TL, Al-Gazali L, Sztriha L, Partlow JN, Kim H, Krup AL, Dammermann A, Krogan N, Walsh CA, Reiter JF. Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication. Elife. 4. PMID 26297806 DOI: 10.7554/Elife.07519 |
0.597 |
|
| 2015 |
Imitola J, Khurana DS, Teplyuk NM, Zucker M, Jethva R, Legido A, Krichevsky AM, Frangieh M, Walsh CA, Carvalho KS. A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephaly. American Journal of Medical Genetics. Part A. PMID 26238961 DOI: 10.1002/ajmg.a.37268 |
0.395 |
|
| 2015 |
Jamuar SS, Walsh CA. Genomic Variants and Variations in Malformations of Cortical Development. Pediatric Clinics of North America. 62: 571-585. PMID 26022163 DOI: 10.1016/j.pcl.2015.03.002 |
0.438 |
|
| 2015 |
Ahmed MY, Chioza BA, Rajab A, Schmitz-Abe K, Al-Khayat A, Al-Turki S, Baple EL, Patton MA, Al-Memar AY, Hurles ME, Partlow JN, Hill RS, Evrony GD, Servattalab S, Markianos K, ... Walsh CA, et al. Loss of PCLO function underlies pontocerebellar hypoplasia type III. Neurology. 84: 1745-50. PMID 25832664 DOI: 10.1212/Wnl.0000000000001523 |
0.703 |
|
| 2015 |
Cai X, Evrony GD, Lehmann HS, Elhosary PC, Mehta BK, Poduri A, Walsh CA. Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain. Cell Reports. 10: 645. PMID 25832109 DOI: 10.1016/j.celrep.2015.01.028 |
0.711 |
|
| 2015 |
Murn J, Zarnack K, Yang YJ, Durak O, Murphy EA, Cheloufi S, Gonzalez DM, Teplova M, Curk T, Zuber J, Patel DJ, Ule J, Luscombe NM, Tsai LH, Walsh CA, et al. Control of a neuronal morphology program by an RNA-binding zinc finger protein, Unkempt. Genes & Development. 29: 501-12. PMID 25737280 DOI: 10.1101/Gad.258483.115 |
0.348 |
|
| 2015 |
Johnson MB, Wang PP, Atabay KD, Murphy EA, Doan RN, Hecht JL, Walsh CA. Single-cell analysis reveals transcriptional heterogeneity of neural progenitors in human cortex. Nature Neuroscience. 18: 637-46. PMID 25734491 DOI: 10.1038/Nn.3980 |
0.807 |
|
| 2015 |
Bae BI, Jayaraman D, Walsh CA. Genetic changes shaping the human brain. Developmental Cell. 32: 423-34. PMID 25710529 DOI: 10.1016/j.devcel.2015.01.035 |
0.624 |
|
| 2015 |
Bulayeva K, Lesch KP, Bulayev O, Walsh C, Glatt S, Gurgenova F, Omarova J, Berdichevets I, Thompson PM. Genomic structural variants are linked with intellectual disability. Journal of Neural Transmission (Vienna, Austria : 1996). PMID 25626716 DOI: 10.1007/S00702-015-1366-8 |
0.381 |
|
| 2015 |
D'Gama AM, Geng Y, Couto JA, Martin B, Boyle EA, LaCoursiere CM, Hossain A, Hatem NE, Barry BJ, Kwiatkowski DJ, Vinters HV, Barkovich AJ, Shendure J, Mathern GW, Walsh CA, et al. Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia. Annals of Neurology. 77: 720-5. PMID 25599672 DOI: 10.1002/Ana.24357 |
0.736 |
|
| 2015 |
Evrony GD, Lee E, Mehta BK, Benjamini Y, Johnson RM, Cai X, Yang L, Haseley P, Lehmann HS, Park PJ, Walsh CA. Cell lineage analysis in human brain using endogenous retroelements. Neuron. 85: 49-59. PMID 25569347 DOI: 10.1016/J.Neuron.2014.12.028 |
0.797 |
|
| 2015 |
Chaste P, Klei L, Sanders SJ, Hus V, Murtha MT, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Mane SM, Martin DM, ... ... Walsh CA, et al. A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Biological Psychiatry. 77: 775-84. PMID 25534755 DOI: 10.1016/J.Biopsych.2014.09.017 |
0.796 |
|
| 2015 |
Kodani A, Yu TW, Johnson JR, Jayaraman D, Johnson TL, Al-Gazali L, Sztriha L, Partlow JN, Kim H, Krup AL, Dammermann A, Krogan NJ, Walsh CA, Reiter JF. Author response: Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication Elife. DOI: 10.7554/Elife.07519.038 |
0.553 |
|
| 2014 |
Hu WF, Pomp O, Ben-Omran T, Kodani A, Henke K, Mochida GH, Yu TW, Woodworth MB, Bonnard C, Raj GS, Tan TT, Hamamy H, Masri A, Shboul M, Al Saffar M, ... ... Walsh CA, et al. Katanin p80 regulates human cortical development by limiting centriole and cilia number. Neuron. 84: 1240-57. PMID 25521379 DOI: 10.1016/J.Neuron.2014.12.017 |
0.76 |
|
| 2014 |
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, ... ... Walsh CA, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.811 |
|
| 2014 |
Hu WF, Chahrour MH, Walsh CA. The diverse genetic landscape of neurodevelopmental disorders. Annual Review of Genomics and Human Genetics. 15: 195-213. PMID 25184530 DOI: 10.1146/annurev-genom-090413-025600 |
0.715 |
|
| 2014 |
Cai X, Evrony GD, Lehmann HS, Elhosary PC, Mehta BK, Poduri A, Walsh CA. Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain. Cell Reports. 8: 1280-9. PMID 25159146 DOI: 10.1016/J.Celrep.2014.07.043 |
0.753 |
|
| 2014 |
Jamuar SS, Lam AT, Kircher M, D'Gama AM, Wang J, Barry BJ, Zhang X, Hill RS, Partlow JN, Rozzo A, Servattalab S, Mehta BK, Topcu M, Amrom D, Andermann E, ... ... Walsh CA, et al. Somatic mutations in cerebral cortical malformations. The New England Journal of Medicine. 371: 733-43. PMID 25140959 DOI: 10.1056/Nejmoa1314432 |
0.824 |
|
| 2014 |
Manzini MC, Xiong L, Shaheen R, Tambunan DE, Di Costanzo S, Mitisalis V, Tischfield DJ, Cinquino A, Ghaziuddin M, Christian M, Jiang Q, Laurent S, Nanjiani ZA, Rasheed S, Hill RS, ... ... Walsh CA, et al. CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasis. Cell Reports. 8: 647-55. PMID 25066123 DOI: 10.1016/j.celrep.2014.06.039 |
0.811 |
|
| 2014 |
Di Costanzo S, Balasubramanian A, Pond HL, Rozkalne A, Pantaleoni C, Saredi S, Gupta VA, Sunu CM, Yu TW, Kang PB, Salih MA, Mora M, Gussoni E, Walsh CA, Manzini MC. POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations. Human Molecular Genetics. 23: 5781-92. PMID 24925318 DOI: 10.1093/hmg/ddu296 |
0.806 |
|
| 2014 |
Chaste P, Sanders SJ, Mohan KN, Klei L, Song Y, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, ... ... Walsh CA, et al. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2. Autism Research : Official Journal of the International Society For Autism Research. 7: 355-62. PMID 24821083 DOI: 10.1002/Aur.1378 |
0.79 |
|
| 2014 |
Zhang X, Ling J, Barcia G, Jing L, Wu J, Barry BJ, Mochida GH, Hill RS, Weimer JM, Stein Q, Poduri A, Partlow JN, Ville D, Dulac O, Yu TW, ... ... Walsh CA, et al. Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. American Journal of Human Genetics. 94: 547-58. PMID 24656866 DOI: 10.1016/J.Ajhg.2014.03.003 |
0.802 |
|
| 2014 |
Walsh CA, Bolger JC, Byrne C, Cocchiglia S, Hao Y, Fagan A, Qin L, Cahalin A, McCartan D, McIlroy M, O'Gaora P, Xu J, Hill AD, Young LS. Global gene repression by the steroid receptor coactivator SRC-1 promotes oncogenesis. Cancer Research. 74: 2533-44. PMID 24648347 DOI: 10.1158/0008-5472.CAN-13-2133 |
0.429 |
|
| 2014 |
Bae BI, Tietjen I, Atabay KD, Evrony GD, Johnson MB, Asare E, Wang PP, Murayama AY, Im K, Lisgo SN, Overman L, Šestan N, Chang BS, Barkovich AJ, Grant PE, ... ... Walsh CA, et al. Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning. Science (New York, N.Y.). 343: 764-8. PMID 24531968 DOI: 10.1126/Science.1244392 |
0.803 |
|
| 2014 |
Reiff RE, Ali BR, Baron B, Yu TW, Ben-Salem S, Coulter ME, Schubert CR, Hill RS, Akawi NA, Al-Younes B, Kaya N, Evrony GD, Al-Saffar M, Felie JM, Partlow JN, ... ... Walsh CA, et al. METTL23, a transcriptional partner of GABPA, is essential for human cognition. Human Molecular Genetics. 23: 3456-66. PMID 24501276 DOI: 10.1093/Hmg/Ddu054 |
0.809 |
|
| 2014 |
Adachi Y, Mochida G, Walsh C, Barkovich J. Posterior fossa in primary microcephaly: Relationships between forebrain and mid-hindbrain size in 110 patients Neuropediatrics. 45: 93-101. PMID 24234199 DOI: 10.1055/S-0033-1360483 |
0.344 |
|
| 2013 |
Poduri A, Heinzen EL, Chitsazzadeh V, Lasorsa FM, Elhosary PC, LaCoursiere CM, Martin E, Yuskaitis CJ, Hill RS, Atabay KD, Barry B, Partlow JN, Bashiri FA, Zeidan RM, Elmalik SA, ... ... Walsh CA, et al. SLC25A22 is a novel gene for migrating partial seizures in infancy. Annals of Neurology. 74: 873-82. PMID 24596948 DOI: 10.1002/Ana.23998 |
0.816 |
|
| 2013 |
Bae BI, Walsh CA. Neuroscience. What are mini-brains? Science (New York, N.Y.). 342: 200-1. PMID 24115427 DOI: 10.1126/science.1245812 |
0.611 |
|
| 2013 |
Wu MP, Doyle JR, Barry B, Beauvais A, Rozkalne A, Piao X, Lawlor MW, Kopin AS, Walsh CA, Gussoni E. G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivo. The Febs Journal. 280: 6097-113. PMID 24102982 DOI: 10.1111/Febs.12529 |
0.315 |
|
| 2013 |
Picker JD, Walsh CA. New innovations: therapeutic opportunities for intellectual disabilities. Annals of Neurology. 74: 382-90. PMID 24038210 DOI: 10.1002/ana.24002 |
0.32 |
|
| 2013 |
Gilmore EC, Walsh CA. Genetic causes of microcephaly and lessons for neuronal development. Wiley Interdisciplinary Reviews. Developmental Biology. 2: 461-78. PMID 24014418 DOI: 10.1002/Wdev.89 |
0.435 |
|
| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Walsh CA, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.777 |
|
| 2013 |
Poduri A, Evrony GD, Cai X, Walsh CA. Somatic mutation, genomic variation, and neurological disease. Science (New York, N.Y.). 341: 1237758. PMID 23828942 DOI: 10.1126/Science.1237758 |
0.763 |
|
| 2013 |
Chaste P, Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, ... ... Walsh CA, et al. Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait. Biological Psychiatry. 74: 576-84. PMID 23746936 DOI: 10.1016/J.Biopsych.2013.04.018 |
0.789 |
|
| 2013 |
Zappaterra MW, LaMantia AS, Walsh CA, Lehtinen MK. Isolation of cerebrospinal fluid from rodent embryos for use with dissected cerebral cortical explants. Journal of Visualized Experiments : Jove. e50333. PMID 23524481 DOI: 10.3791/50333 |
0.735 |
|
| 2013 |
Stevens E, Carss KJ, Cirak S, Foley AR, Torelli S, Willer T, Tambunan DE, Yau S, Brodd L, Sewry CA, Feng L, Haliloglu G, Orhan D, Dobyns WB, Enns GM, ... ... Walsh CA, et al. Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan. American Journal of Human Genetics. 92: 354-65. PMID 23453667 DOI: 10.1016/J.Ajhg.2013.01.016 |
0.748 |
|
| 2013 |
Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, ... ... Walsh CA, et al. Using whole-exome sequencing to identify inherited causes of autism. Neuron. 77: 259-73. PMID 23352163 DOI: 10.1016/J.Neuron.2012.11.002 |
0.821 |
|
| 2013 |
Dies KA, Bodell A, Hisama FM, Guo CY, Barry B, Chang BS, Barkovich AJ, Walsh CA. Schizencephaly: association with young maternal age, alcohol use, and lack of prenatal care. Journal of Child Neurology. 28: 198-203. PMID 23266945 DOI: 10.1177/0883073812467850 |
0.328 |
|
| 2013 |
Akawi NA, Canpolat FE, White SM, Quilis-Esquerra J, Morales Sanchez M, Gamundi MJ, Mochida GH, Walsh CA, Ali BR, Al-Gazali L. Delineation of the clinical, molecular and cellular aspects of novel JAM3 mutations underlying the autosomal recessive hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. Human Mutation. 34: 498-505. PMID 23255084 DOI: 10.1002/humu.22263 |
0.415 |
|
| 2013 |
González G, Vedolin L, Barry B, Poduri A, Walsh C, Barkovich AJ. Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI. Ajnr. American Journal of Neuroradiology. 34: 877-83. PMID 23064591 DOI: 10.3174/ajnr.A3312 |
0.332 |
|
| 2013 |
Yu TW, Coulter M, Chahrour M, Walsh CA. Autism Spectrum Disorders Genomic and Personalized Medicine. 2: 1067-1074. DOI: 10.1016/B978-0-12-382227-7.00090-2 |
0.773 |
|
| 2012 |
Yang YJ, Baltus AE, Mathew RS, Murphy EA, Evrony GD, Gonzalez DM, Wang EP, Marshall-Walker CA, Barry BJ, Murn J, Tatarakis A, Mahajan MA, Samuels HH, Shi Y, Golden JA, ... ... Walsh CA, et al. Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation. Cell. 151: 1097-112. PMID 23178126 DOI: 10.1016/J.Cell.2012.10.043 |
0.809 |
|
| 2012 |
Evrony GD, Cai X, Lee E, Hills LB, Elhosary PC, Lehmann HS, Parker JJ, Atabay KD, Gilmore EC, Poduri A, Park PJ, Walsh CA. Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain. Cell. 151: 483-96. PMID 23101622 DOI: 10.1016/J.Cell.2012.09.035 |
0.815 |
|
| 2012 |
Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin CL, ... ... Walsh CA, et al. Common genetic variants, acting additively, are a major source of risk for autism. Molecular Autism. 3: 9. PMID 23067556 DOI: 10.1186/2040-2392-3-9 |
0.795 |
|
| 2012 |
Mochida GH, Ganesh VS, de Michelena MI, Dias H, Atabay KD, Kathrein KL, Huang HT, Hill RS, Felie JM, Rakiec D, Gleason D, Hill AD, Malik AN, Barry BJ, Partlow JN, ... ... Walsh CA, et al. CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Nature Genetics. 44: 1260-4. PMID 23023333 DOI: 10.1038/Ng.2425 |
0.802 |
|
| 2012 |
Manzini MC, Tambunan DE, Hill RS, Yu TW, Maynard TM, Heinzen EL, Shianna KV, Stevens CR, Partlow JN, Barry BJ, Rodriguez J, Gupta VA, Al-Qudah AK, Eyaid WM, Friedman JM, ... ... Walsh CA, et al. Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome. American Journal of Human Genetics. 91: 541-7. PMID 22958903 DOI: 10.1016/J.Ajhg.2012.07.009 |
0.821 |
|
| 2012 |
Liu JS, Schubert CR, Fu X, Fourniol FJ, Jaiswal JK, Houdusse A, Stultz CM, Moores CA, Walsh CA. Molecular basis for specific regulation of neuronal kinesin-3 motors by doublecortin family proteins. Molecular Cell. 47: 707-21. PMID 22857951 DOI: 10.1016/J.Molcel.2012.06.025 |
0.657 |
|
| 2012 |
Poduri A, Chopra SS, Neilan EG, Elhosary PC, Kurian MA, Meyer E, Barry BJ, Khwaja OS, Salih MA, Stödberg T, Scheffer IE, Maher ER, Sahin M, Wu BL, Berry GT, ... Walsh CA, et al. Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy. Epilepsia. 53: e146-50. PMID 22690784 DOI: 10.1111/J.1528-1167.2012.03538.X |
0.398 |
|
| 2012 |
Chahrour MH, Yu TW, Lim ET, Ataman B, Coulter ME, Hill RS, Stevens CR, Schubert CR, Greenberg ME, Gabriel SB, Walsh CA. Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. Plos Genetics. 8: e1002635. PMID 22511880 DOI: 10.1371/Journal.Pgen.1002635 |
0.835 |
|
| 2012 |
Reynolds JJ, Walker AK, Gilmore EC, Walsh CA, Caldecott KW. Impact of PNKP mutations associated with microcephaly, seizures and developmental delay on enzyme activity and DNA strand break repair. Nucleic Acids Research. 40: 6608-19. PMID 22508754 DOI: 10.1093/Nar/Gks318 |
0.336 |
|
| 2012 |
Poduri A, Evrony GD, Cai X, Elhosary PC, Beroukhim R, Lehtinen MK, Hills LB, Heinzen EL, Hill A, Hill RS, Barry BJ, Bourgeois BF, Riviello JJ, Barkovich AJ, Black PM, ... ... Walsh CA, et al. Somatic activation of AKT3 causes hemispheric developmental brain malformations. Neuron. 74: 41-8. PMID 22500628 DOI: 10.1016/J.Neuron.2012.03.010 |
0.829 |
|
| 2012 |
Marangi G, Orteschi D, Vigevano F, Felie J, Walsh CA, Manzini MC, Neri G. Expanding the spectrum of rearrangements involving chromosome 19: a mild phenotype associated with a 19p13.12-p13.13 deletion. American Journal of Medical Genetics. Part A. 158: 888-93. PMID 22419660 DOI: 10.1002/ajmg.a.35254 |
0.737 |
|
| 2012 |
Clapham KR, Yu TW, Ganesh VS, Barry B, Chan Y, Mei D, Parrini E, Funalot B, Dupuis L, Nezarati MM, du Souich C, van Karnebeek C, Guerrini R, Walsh CA. FLNA genomic rearrangements cause periventricular nodular heterotopia. Neurology. 78: 269-78. PMID 22238415 DOI: 10.1212/Wnl.0B013E31824365E4 |
0.774 |
|
| 2012 |
Ganesh V, Poduri A, Yu T, Partlow J, Barry B, Gotoff J, Walsh C. ISDN2012_0212: Whole exome sequencing of right‐sided asymmetric polymicrogyria International Journal of Developmental Neuroscience. 30: 682-682. DOI: 10.1016/J.Ijdevneu.2012.10.035 |
0.735 |
|
| 2011 |
Di Blasi C, Bellafiore E, Salih MA, Manzini MC, Moore SA, Seidahmed MZ, Mukhtar MM, Karrar ZA, Walsh CA, Campbell KP, Mantegazza R, Morandi L, Mora M. Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2. Bmc Research Notes. 4: 534. PMID 22166137 DOI: 10.1186/1756-0500-4-534 |
0.736 |
|
| 2011 |
Ben-Omran T, Ali R, Almureikhi M, Alameer S, Al-Saffar M, Walsh CA, Felie JM, Teebi A. Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 gene. American Journal of Medical Genetics. Part A. 155: 2647-53. PMID 21964978 DOI: 10.1002/ajmg.a.34219 |
0.342 |
|
| 2011 |
Lehtinen MK, Walsh CA. Neurogenesis at the brain-cerebrospinal fluid interface. Annual Review of Cell and Developmental Biology. 27: 653-79. PMID 21801012 DOI: 10.1146/Annurev-Cellbio-092910-154026 |
0.635 |
|
| 2011 |
Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, ... ... Walsh CA, et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85. PMID 21658581 DOI: 10.1016/J.Neuron.2011.05.002 |
0.798 |
|
| 2011 |
Labelle-Dumais C, Dilworth DJ, Harrington EP, de Leau M, Lyons D, Kabaeva Z, Manzini MC, Dobyns WB, Walsh CA, Michele DE, Gould DB. COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans. Plos Genetics. 7: e1002062. PMID 21625620 DOI: 10.1371/Journal.Pgen.1002062 |
0.768 |
|
| 2011 |
Alkuraya FS, Cai X, Emery C, Mochida GH, Al-Dosari MS, Felie JM, Hill RS, Barry BJ, Partlow JN, Gascon GG, Kentab A, Jan M, Shaheen R, Feng Y, Walsh CA. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]. American Journal of Human Genetics. 88: 536-47. PMID 21529751 DOI: 10.1016/J.Ajhg.2011.04.003 |
0.478 |
|
| 2011 |
Adachi Y, Poduri A, Kawaguch A, Yoon G, Salih MA, Yamashita F, Walsh CA, Barkovich AJ. Congenital microcephaly with a simplified gyral pattern: associated findings and their significance. Ajnr. American Journal of Neuroradiology. 32: 1123-9. PMID 21454410 DOI: 10.3174/ajnr.A2440 |
0.303 |
|
| 2011 |
Lehtinen MK, Zappaterra MW, Chen X, Yang YJ, Hill AD, Lun M, Maynard T, Gonzalez D, Kim S, Ye P, D'Ercole AJ, Wong ET, LaMantia AS, Walsh CA. The cerebrospinal fluid provides a proliferative niche for neural progenitor cells. Neuron. 69: 893-905. PMID 21382550 DOI: 10.1016/J.Neuron.2011.01.023 |
0.778 |
|
| 2011 |
Liu GH, Barkho BZ, Ruiz S, Diep D, Qu J, Yang SL, Panopoulos AD, Suzuki K, Kurian L, Walsh C, Thompson J, Boue S, Fung HL, Sancho-Martinez I, Zhang K, et al. Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome. Nature. 472: 221-5. PMID 21346760 DOI: 10.1038/Nature09879 |
0.334 |
|
| 2011 |
Manzini MC, Walsh CA. What disorders of cortical development tell us about the cortex: one plus one does not always make two. Current Opinion in Genetics & Development. 21: 333-9. PMID 21288712 DOI: 10.1016/j.gde.2011.01.006 |
0.741 |
|
| 2011 |
Dwyer ND, Manning DK, Moran JL, Mudbhary R, Fleming MS, Favero CB, Vock VM, O'Leary DD, Walsh CA, Beier DR. A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype. Neural Development. 6: 3. PMID 21214893 DOI: 10.1186/1749-8104-6-3 |
0.803 |
|
| 2011 |
Alkuraya F, Cai X, Emery C, Mochida G, Al-Dosari M, Felie J, Hill R, Barry B, Partlow J, Gascon G, Kentab A, Jan M, Shaheen R, Feng Y, Walsh C. Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly The American Journal of Human Genetics. 88: 677. DOI: 10.1016/J.Ajhg.2011.04.020 |
0.385 |
|
| 2010 |
Mochida GH, Ganesh VS, Felie JM, Gleason D, Hill RS, Clapham KR, Rakiec D, Tan WH, Akawi N, Al-Saffar M, Partlow JN, Tinschert S, Barkovich AJ, Ali B, Al-Gazali L, ... Walsh CA, et al. A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. American Journal of Human Genetics. 87: 882-9. PMID 21109224 DOI: 10.1016/J.Ajhg.2010.10.026 |
0.751 |
|
| 2010 |
Birk E, Har-Zahav A, Manzini CM, Pasmanik-Chor M, Kornreich L, Walsh CA, Noben-Trauth K, Albin A, Simon AJ, Colleaux L, Morad Y, Rainshtein L, Tischfield DJ, Wang P, Magal N, et al. SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system. American Journal of Human Genetics. 87: 694-700. PMID 21035105 DOI: 10.1016/J.Ajhg.2010.10.005 |
0.425 |
|
| 2010 |
Walsh CA, Engle EC. Allelic diversity in human developmental neurogenetics: insights into biology and disease. Neuron. 68: 245-53. PMID 20955932 DOI: 10.1016/J.Neuron.2010.09.042 |
0.42 |
|
| 2010 |
Mellado C, Poduri A, Gleason D, Elhosary PC, Barry BJ, Partlow JN, Chang BS, Shaw GM, Barkovich AJ, Walsh CA. Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort. American Journal of Medical Genetics. Part A. 152: 2736-42. PMID 20949537 DOI: 10.1002/Ajmg.A.33684 |
0.435 |
|
| 2010 |
Yu TW, Mochida GH, Tischfield DJ, Sgaier SK, Flores-Sarnat L, Sergi CM, Topçu M, McDonald MT, Barry BJ, Felie JM, Sunu C, Dobyns WB, Folkerth RD, Barkovich AJ, Walsh CA. Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nature Genetics. 42: 1015-20. PMID 20890278 DOI: 10.1038/Ng.683 |
0.709 |
|
| 2010 |
Sheen VL, Torres AR, Du X, Barry B, Walsh CA, Kimonis VE. Mutation in PQBP1 is associated with periventricular heterotopia. American Journal of Medical Genetics. Part A. 152: 2888-90. PMID 20886605 DOI: 10.1002/ajmg.a.33507 |
0.445 |
|
| 2010 |
Cubelos B, Sebastián-Serrano A, Beccari L, Calcagnotto ME, Cisneros E, Kim S, Dopazo A, Alvarez-Dolado M, Redondo JM, Bovolenta P, Walsh CA, Nieto M. Cux1 and Cux2 regulate dendritic branching, spine morphology, and synapses of the upper layer neurons of the cortex. Neuron. 66: 523-35. PMID 20510857 DOI: 10.1016/J.Neuron.2010.04.038 |
0.669 |
|
| 2010 |
Ching MS, Shen Y, Tan WH, Jeste SS, Morrow EM, Chen X, Mukaddes NM, Yoo SY, Hanson E, Hundley R, Austin C, Becker RE, Berry GT, Driscoll K, Engle EC, ... ... Walsh CA, et al. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 937-47. PMID 20468056 DOI: 10.1002/Ajmg.B.31063 |
0.766 |
|
| 2010 |
Lizarraga SB, Margossian SP, Harris MH, Campagna DR, Han AP, Blevins S, Mudbhary R, Barker JE, Walsh CA, Fleming MD. Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors. Development (Cambridge, England). 137: 1907-17. PMID 20460369 DOI: 10.1242/dev.040410 |
0.83 |
|
| 2010 |
Manzini MC, Rajab A, Maynard TM, Mochida GH, Tan WH, Nasir R, Hill RS, Gleason D, Al Saffar M, Partlow JN, Barry BJ, Vernon M, LaMantia AS, Walsh CA. Developmental and degenerative features in a complicated spastic paraplegia. Annals of Neurology. 67: 516-25. PMID 20437587 DOI: 10.1002/Ana.21923 |
0.813 |
|
| 2010 |
Kim S, Lehtinen MK, Sessa A, Zappaterra MW, Cho SH, Gonzalez D, Boggan B, Austin CA, Wijnholds J, Gambello MJ, Malicki J, LaMantia AS, Broccoli V, Walsh CA. The apical complex couples cell fate and cell survival to cerebral cortical development. Neuron. 66: 69-84. PMID 20399730 DOI: 10.1016/J.Neuron.2010.03.019 |
0.759 |
|
| 2010 |
Silver DL, Watkins-Chow DE, Schreck KC, Pierfelice TJ, Larson DM, Burnetti AJ, Liaw HJ, Myung K, Walsh CA, Gaiano N, Pavan WJ. The exon junction complex component Magoh controls brain size by regulating neural stem cell division. Nature Neuroscience. 13: 551-8. PMID 20364144 DOI: 10.1038/Nn.2527 |
0.393 |
|
| 2010 |
Amrom D, Walsh CA. Genetic malformations of the human frontal lobe. Epilepsia. 51: 13-6. PMID 20331705 DOI: 10.1111/j.1528-1167.2009.02435.x |
0.342 |
|
| 2010 |
Shen Y, Dies KA, Holm IA, Bridgemohan C, Sobeih MM, Caronna EB, Miller KJ, Frazier JA, Silverstein I, Picker J, Weissman L, Raffalli P, Jeste S, Demmer LA, Peters HK, ... ... Walsh CA, et al. Clinical genetic testing for patients with autism spectrum disorders. Pediatrics. 125: e727-35. PMID 20231187 DOI: 10.1542/Peds.2009-1684 |
0.322 |
|
| 2010 |
Shen J, Gilmore EC, Marshall CA, Haddadin M, Reynolds JJ, Eyaid W, Bodell A, Barry B, Gleason D, Allen K, Ganesh VS, Chang BS, Grix A, Hill RS, Topcu M, ... ... Walsh CA, et al. Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nature Genetics. 42: 245-9. PMID 20118933 DOI: 10.1038/Ng.526 |
0.745 |
|
| 2010 |
Powers SE, Taniguchi K, Yen W, Melhuish TA, Shen J, Walsh CA, Sutherland AE, Wotton D. Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation. Development (Cambridge, England). 137: 249-59. PMID 20040491 DOI: 10.1242/Dev.040782 |
0.487 |
|
| 2010 |
Poduri A, Chitsazzadeh V, D'Arrigo S, Fedrizzi E, Pantaleoni C, Riva D, Busse C, Küster H, Duplessis A, Gaitanis J, Sahin M, Garganta C, Topcu M, Dies KA, Barry BJ, ... ... Walsh CA, et al. The syndrome of perisylvian polymicrogyria with congenital arthrogryposis. Brain & Development. 32: 550-5. PMID 19751967 DOI: 10.1016/J.Braindev.2009.08.005 |
0.348 |
|
| 2010 |
Liu JS, Walsh CA. Rare genetic causes of lissencephaly may implicate microtubule-based transport in the pathogenesis of cortical dysplasias Epilepsia. 51: 67. DOI: 10.1111/J.1528-1167.2010.02853.X |
0.521 |
|
| 2010 |
Yang Y, Baltus AE, Marshall C, Wang E, Gleason D, Walsh CA. Essential roles of a novel zinc finger protein in human cerebral cortical development International Journal of Developmental Neuroscience. 28: 684. DOI: 10.1016/J.Ijdevneu.2010.07.126 |
0.329 |
|
| 2010 |
Vock VM, Fleming M, Rasoul B, Beier D, Walsh C, Dwyer ND. Abnormal cortical development and cell division defects in magoo mutant mice International Journal of Developmental Neuroscience. 28: 656-657. DOI: 10.1016/J.Ijdevneu.2010.07.046 |
0.571 |
|
| 2010 |
Ferland RJ, Walsh CA. Joubert Syndrome Encyclopedia of Neuroscience. 249-256. DOI: 10.1016/B978-008045046-9.01487-X |
0.587 |
|
| 2009 |
Mochida GH, Mahajnah M, Hill AD, Basel-Vanagaite L, Gleason D, Hill RS, Bodell A, Crosier M, Straussberg R, Walsh CA. A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly. American Journal of Human Genetics. 85: 897-902. PMID 20004763 DOI: 10.1016/j.ajhg.2009.10.027 |
0.643 |
|
| 2009 |
Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, Hill RS, Risch N, Hauser WA, Pedley TA, Walsh CA, Ottman R. Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+. Neurology. 73: 1264-72. PMID 19841378 DOI: 10.1212/Wnl.0B013E3181Bd10D3 |
0.358 |
|
| 2009 |
Yu F, Keinan A, Chen H, Ferland RJ, Hill RS, Mignault AA, Walsh CA, Reich D. Detecting natural selection by empirical comparison to random regions of the genome. Human Molecular Genetics. 18: 4853-67. PMID 19783549 DOI: 10.1093/Hmg/Ddp457 |
0.677 |
|
| 2009 |
Travaglini L, Brancati F, Attie-Bitach T, Audollent S, Bertini E, Kaplan J, Perrault I, Iannicelli M, Mancuso B, Rigoli L, Rozet JM, Swistun D, Tolentino J, Dallapiccola B, Gleeson JG, ... ... Walsh CA, et al. Expanding CEP290 mutational spectrum in ciliopathies. American Journal of Medical Genetics. Part A. 149: 2173-80. PMID 19764032 DOI: 10.1002/Ajmg.A.33025 |
0.614 |
|
| 2009 |
Huang Z, Kawase-Koga Y, Zhang S, Visvader J, Toth M, Walsh CA, Sun T. Transcription factor Lmo4 defines the shape of functional areas in developing cortices and regulates sensorimotor control. Developmental Biology. 327: 132-42. PMID 19111533 DOI: 10.1016/J.Ydbio.2008.12.003 |
0.457 |
|
| 2009 |
Parrini E, Ferrari AR, Dorn T, Walsh CA, Guerrini R. Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations. Epilepsia. 50: 1344-53. PMID 19016831 DOI: 10.1111/j.1528-1167.2008.01787.x |
0.416 |
|
| 2009 |
Ferland RJ, Batiz LF, Neal J, Lian G, Bundock E, Lu J, Hsiao YC, Diamond R, Mei D, Banham AH, Brown PJ, Vanderburg CR, Joseph J, Hecht JL, Folkerth R, ... ... Walsh CA, et al. Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. Human Molecular Genetics. 18: 497-516. PMID 18996916 DOI: 10.1093/Hmg/Ddn377 |
0.828 |
|
| 2009 |
Walsh CA. Molecular Genetics of Human Developmental Brain Disorders of the Arabian Gulf Region Journal of Medical Sciences. 2: 5-12. DOI: 10.2174/1996327000902010005 |
0.398 |
|
| 2009 |
Manzini M, Gleason D, Chang B, Hill R, Partlow J, Barry B, Poduri A, Basel-Vanagaite L, Seidhamed M, Salih M, Dobyns W, Walsh C. EM.P.2.04 Unraveling the genetic complexity of alpha-dystroglycanopathies: Ethnically diverse pathogenic mutations Neuromuscular Disorders. 19: 552-553. DOI: 10.1016/J.Nmd.2009.06.033 |
0.708 |
|
| 2008 |
Alazami AM, Al-Saif A, Al-Semari A, Bohlega S, Zlitni S, Alzahrani F, Bavi P, Kaya N, Colak D, Khalak H, Baltus A, Peterlin B, Danda S, Bhatia KP, Schneider SA, ... ... Walsh CA, et al. Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. American Journal of Human Genetics. 83: 684-91. PMID 19026396 DOI: 10.1016/J.Ajhg.2008.10.018 |
0.414 |
|
| 2008 |
Walsh CA, Morrow EM, Rubenstein JL. Autism and brain development. Cell. 135: 396-400. PMID 18984148 DOI: 10.1016/j.cell.2008.10.015 |
0.739 |
|
| 2008 |
Morrow EM, Kane A, Goff DC, Walsh CA. Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairment. Schizophrenia Research. 106: 265-7. PMID 18805672 DOI: 10.1016/J.Schres.2008.08.021 |
0.67 |
|
| 2008 |
Manzini MC, Gleason D, Chang BS, Hill RS, Barry BJ, Partlow JN, Poduri A, Currier S, Galvin-Parton P, Shapiro LR, Schmidt K, Davis JG, Basel-Vanagaite L, Seidahmed MZ, Salih MA, ... ... Walsh CA, et al. Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East. Human Mutation. 29: E231-41. PMID 18752264 DOI: 10.1002/Humu.20844 |
0.819 |
|
| 2008 |
Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, ... ... Walsh CA, et al. Identifying autism loci and genes by tracing recent shared ancestry. Science (New York, N.Y.). 321: 218-23. PMID 18621663 DOI: 10.1126/Science.1157657 |
0.831 |
|
| 2008 |
Sepp KJ, Hong P, Lizarraga SB, Liu JS, Mejia LA, Walsh CA, Perrimon N. Identification of neural outgrowth genes using genome-wide RNAi. Plos Genetics. 4: e1000111. PMID 18604272 DOI: 10.1371/Journal.Pgen.1000111 |
0.818 |
|
| 2008 |
Kantarci S, Ragge NK, Thomas NS, Robinson DO, Noonan KM, Russell MK, Donnai D, Raymond FL, Walsh CA, Donahoe PK, Pober BR. Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy. American Journal of Medical Genetics. Part A. 146: 1842-7. PMID 18553518 DOI: 10.1002/Ajmg.A.32381 |
0.401 |
|
| 2008 |
Li S, Jin Z, Koirala S, Bu L, Xu L, Hynes RO, Walsh CA, Corfas G, Piao X. GPR56 regulates pial basement membrane integrity and cortical lamination. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 5817-26. PMID 18509043 DOI: 10.1523/Jneurosci.0853-08.2008 |
0.434 |
|
| 2008 |
Pawlisz AS, Mutch C, Wynshaw-Boris A, Chenn A, Walsh CA, Feng Y. Lis1-Nde1-dependent neuronal fate control determines cerebral cortical size and lamination. Human Molecular Genetics. 17: 2441-55. PMID 18469343 DOI: 10.1093/Hmg/Ddn144 |
0.817 |
|
| 2008 |
Cubelos B, Sebastián-Serrano A, Kim S, Redondo JM, Walsh C, Nieto M. Cux-1 and Cux-2 control the development of Reelin expressing cortical interneurons. Developmental Neurobiology. 68: 917-925. PMID 18327765 DOI: 10.1002/Dneu.20626 |
0.701 |
|
| 2008 |
Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, et al. Association between microdeletion and microduplication at 16p11.2 and autism. The New England Journal of Medicine. 358: 667-75. PMID 18184952 DOI: 10.1056/Nejmoa075974 |
0.546 |
|
| 2008 |
Cubelos B, Sebastián-Serrano A, Kim S, Moreno-Ortiz C, Redondo JM, Walsh CA, Nieto M. Cux-2 controls the proliferation of neuronal intermediate precursors of the cortical subventricular zone. Cerebral Cortex (New York, N.Y. : 1991). 18: 1758-70. PMID 18033766 DOI: 10.1093/Cercor/Bhm199 |
0.675 |
|
| 2008 |
Teber S, Sezer T, Kafali M, Manzini MC, Konuk Yüksel B, Tekin M, Fitöz S, Walsh CA, Deda G. Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 12: 133-6. PMID 17881266 DOI: 10.1016/j.ejpn.2007.06.008 |
0.744 |
|
| 2007 |
Chae TH, Walsh CA. Genes that control the size of the cerebral cortex. Novartis Foundation Symposium. 288: 79-90; discussion 91. PMID 18494253 DOI: 10.1002/9780470994030.ch6 |
0.818 |
|
| 2007 |
Chang BS, Katzir T, Liu T, Corriveau K, Barzillai M, Apse KA, Bodell A, Hackney D, Alsop D, Wong ST, Wong S, Walsh CA. A structural basis for reading fluency: white matter defects in a genetic brain malformation. Neurology. 69: 2146-54. PMID 18056578 DOI: 10.1212/01.Wnl.0000286365.41070.54 |
0.359 |
|
| 2007 |
Rajab A, Manzini MC, Mochida GH, Walsh CA, Ross ME. A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia. American Journal of Medical Genetics. Part A. 143: 2761-7. PMID 17975804 DOI: 10.1002/ajmg.a.31955 |
0.726 |
|
| 2007 |
Zhang Y, Ryan JA, Di Cesare PE, Liu J, Walsh CA, You Z. Doublecortin is expressed in articular chondrocytes. Biochemical and Biophysical Research Communications. 363: 694-700. PMID 17897623 DOI: 10.1016/J.Bbrc.2007.09.030 |
0.443 |
|
| 2007 |
Zappaterra MD, Lisgo SN, Lindsay S, Gygi SP, Walsh CA, Ballif BA. A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid. Journal of Proteome Research. 6: 3537-48. PMID 17696520 DOI: 10.1021/Pr070247W |
0.781 |
|
| 2007 |
Kantarci S, Al-Gazali L, Hill RS, Donnai D, Black GC, Bieth E, Chassaing N, Lacombe D, Devriendt K, Teebi A, Loscertales M, Robson C, Liu T, MacLaughlin DT, Noonan KM, ... ... Walsh CA, et al. Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes. Nature Genetics. 39: 957-9. PMID 17632512 DOI: 10.1038/Ng2063 |
0.358 |
|
| 2007 |
Hill AD, Chang BS, Hill RS, Garraway LA, Bodell A, Sellers WR, Walsh CA. A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome. American Journal of Medical Genetics. Part A. 143: 1692-8. PMID 17603806 DOI: 10.1002/Ajmg.A.31776 |
0.495 |
|
| 2007 |
Jin Z, Tietjen I, Bu L, Liu-Yesucevitz L, Gaur SK, Walsh CA, Piao X. Disease-associated mutations affect GPR56 protein trafficking and cell surface expression. Human Molecular Genetics. 16: 1972-85. PMID 17576745 DOI: 10.1093/Hmg/Ddm144 |
0.396 |
|
| 2007 |
Lu W, Quintero-Rivera F, Fan Y, Alkuraya FS, Donovan DJ, Xi Q, Turbe-Doan A, Li QG, Campbell CG, Shanske AL, Sherr EH, Ahmad A, Peters R, Rilliet B, Parvex P, ... ... Walsh CA, et al. NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. Plos Genetics. 3: e80. PMID 17530927 DOI: 10.1371/Journal.Pgen.0030080 |
0.385 |
|
| 2007 |
Lu J, Lian G, Lenkinski R, De Grand A, Vaid RR, Bryce T, Stasenko M, Boskey A, Walsh C, Sheen V. Filamin B mutations cause chondrocyte defects in skeletal development. Human Molecular Genetics. 16: 1661-75. PMID 17510210 DOI: 10.1093/Hmg/Ddm114 |
0.362 |
|
| 2007 |
Tietjen I, Bodell A, Apse K, Mendonza AM, Chang BS, Shaw GM, Barkovich AJ, Lammer EJ, Walsh CA. Comprehensive EMX2 genotyping of a large schizencephaly case series. American Journal of Medical Genetics. Part A. 143: 1313-6. PMID 17506092 DOI: 10.1002/Ajmg.A.31767 |
0.435 |
|
| 2007 |
Yu F, Hill RS, Schaffner SF, Sabeti PC, Wang ET, Mignault AA, Ferland RJ, Moyzis RK, Walsh CA, Reich D. Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens". Science (New York, N.Y.). 316: 370. PMID 17446375 DOI: 10.1126/Science.1137568 |
0.643 |
|
| 2007 |
Friocourt G, Liu JS, Antypa M, Rakic S, Walsh CA, Parnavelas JG. Both doublecortin and doublecortin-like kinase play a role in cortical interneuron migration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 3875-83. PMID 17409252 DOI: 10.1523/Jneurosci.4530-06.2007 |
0.582 |
|
| 2007 |
Neal J, Takahashi M, Silva M, Tiao G, Walsh CA, Sheen VL. Insights into the gyrification of developing ferret brain by magnetic resonance imaging. Journal of Anatomy. 210: 66-77. PMID 17229284 DOI: 10.1111/J.1469-7580.2006.00674.X |
0.708 |
|
| 2007 |
Chang BS, Duzcan F, Kim S, Cinbis M, Aggarwal A, Apse KA, Ozdel O, Atmaca M, Zencir S, Bagci H, Walsh CA. The role of RELN in lissencephaly and neuropsychiatric disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 58-63. PMID 16958033 DOI: 10.1002/ajmg.b.30392 |
0.487 |
|
| 2007 |
Avila P, Hill A, Walsh C. Refining a locus for pontocerebellar hypoplasia 3; a human genetics linkage inquiry Developmental Biology. 306: 379. DOI: 10.1016/j.ydbio.2007.03.349 |
0.523 |
|
| 2006 |
Feng Y, Chen MH, Moskowitz IP, Mendonza AM, Vidali L, Nakamura F, Kwiatkowski DJ, Walsh CA. Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis. Proceedings of the National Academy of Sciences of the United States of America. 103: 19836-41. PMID 17172441 DOI: 10.1073/pnas.0609628104 |
0.409 |
|
| 2006 |
Amadio JP, Walsh CA. Brain evolution and uniqueness in the human genome. Cell. 126: 1033-5. PMID 16990130 DOI: 10.1016/j.cell.2006.09.007 |
0.336 |
|
| 2006 |
Neal J, Raju GP, Bodell A, Apse K, Walsh CA, Sheen VL. Periventricular heterotopia with complete agenesis of the corpus callosum : a case report. Journal of Neurology. 253: 1358-9. PMID 16906346 DOI: 10.1007/S00415-006-0182-3 |
0.62 |
|
| 2006 |
Sun T, Walsh CA. Molecular approaches to brain asymmetry and handedness. Nature Reviews. Neuroscience. 7: 655-62. PMID 16858393 DOI: 10.1038/nrn1930 |
0.385 |
|
| 2006 |
Neal J, Apse K, Sahin M, Walsh CA, Sheen VL. Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia. American Journal of Medical Genetics. Part A. 140: 1692-5. PMID 16835933 DOI: 10.1002/Ajmg.A.31334 |
0.666 |
|
| 2006 |
Basel-Vanagaite L, Muncher L, Straussberg R, Pasmanik-Chor M, Yahav M, Rainshtein L, Walsh CA, Magal N, Taub E, Drasinover V, Shalev H, Attia R, Rechavi G, Simon AJ, Shohat M. Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis. Annals of Neurology. 60: 214-22. PMID 16786527 DOI: 10.1002/Ana.20902 |
0.435 |
|
| 2006 |
Sun T, Collura RV, Ruvolo M, Walsh CA. Genomic and evolutionary analyses of asymmetrically expressed genes in human fetal left and right cerebral cortex. Cerebral Cortex (New York, N.Y. : 1991). 16: i18-25. PMID 16766703 DOI: 10.1093/Cercor/Bhk026 |
0.458 |
|
| 2006 |
Rajab A, Yoo SY, Abdulgalil A, Kathiri S, Ahmed R, Mochida GH, Bodell A, Barkovich AJ, Walsh CA. An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation. American Journal of Medical Genetics. Part A. 140: 1504-10. PMID 16761294 DOI: 10.1002/ajmg.a.31288 |
0.528 |
|
| 2006 |
Ferland RJ, Gaitanis JN, Apse K, Tantravahi U, Walsh CA, Sheen VL. Periventricular nodular heterotopia and Williams syndrome. American Journal of Medical Genetics. Part A. 140: 1305-11. PMID 16691586 DOI: 10.1002/Ajmg.A.31259 |
0.688 |
|
| 2006 |
Parrini E, Ramazzotti A, Dobyns WB, Mei D, Moro F, Veggiotti P, Marini C, Brilstra EH, Dalla Bernardina B, Goodwin L, Bodell A, Jones MC, Nangeroni M, Palmeri S, Said E, ... ... Walsh CA, et al. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations. Brain : a Journal of Neurology. 129: 1892-906. PMID 16684786 DOI: 10.1093/brain/awl125 |
0.444 |
|
| 2006 |
Sheen VL, Ferland RJ, Harney M, Hill RS, Neal J, Banham AH, Brown P, Chenn A, Corbo J, Hecht J, Folkerth R, Walsh CA. Impaired proliferation and migration in human Miller-Dieker neural precursors. Annals of Neurology. 60: 137-44. PMID 16642511 DOI: 10.1002/Ana.20843 |
0.82 |
|
| 2006 |
Tsao JW, Neal J, Apse K, Stephan MJ, Dobyns WB, Hill RS, Walsh CA, Sheen VL. Cerebellar ataxia with progressive improvement. Archives of Neurology. 63: 594-7. PMID 16606775 DOI: 10.1001/Archneur.63.4.594 |
0.66 |
|
| 2006 |
Gérard-Blanluet M, Sheen V, Machinis K, Neal J, Apse K, Danan C, Sinico M, Brugières P, Mage K, Ratsimbazafy L, Elbez A, Janaud JC, Amselem S, Walsh C, Encha-Razavi F. Bilateral periventricular heterotopias in an X-linked dominant transmission in a family with two affected males. American Journal of Medical Genetics. Part A. 140: 1041-6. PMID 16596669 DOI: 10.1002/Ajmg.A.31197 |
0.688 |
|
| 2006 |
Olson EC, Kim S, Walsh CA. Impaired neuronal positioning and dendritogenesis in the neocortex after cell-autonomous Dab1 suppression. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 1767-75. PMID 16467525 DOI: 10.1523/JNEUROSCI.3000-05.2006 |
0.354 |
|
| 2006 |
Sheen VL, Ferland RJ, Neal J, Harney M, Hill RS, Banham A, Brown P, Chenn A, Corbo J, Hecht J, Folkerth R, Walsh CA. Neocortical neuronal arrangement in Miller Dieker syndrome. Acta Neuropathologica. 111: 489-96. PMID 16456669 DOI: 10.1007/S00401-005-0010-3 |
0.814 |
|
| 2006 |
Masruha MR, Caboclo LO, Carrete H, Cendes IL, Rodrigues MG, Garzon E, Yacubian EM, Sakamoto AC, Sheen V, Harney M, Neal J, Hill RS, Bodell A, Walsh C, Vilanova LC. Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in males. Epilepsia. 47: 211-4. PMID 16417552 DOI: 10.1111/J.1528-1167.2006.00390.X |
0.713 |
|
| 2006 |
Chang BS, Apse KA, Caraballo R, Cross JH, Mclellan A, Jacobson RD, Valente KD, Barkovich AJ, Walsh CA. A familial syndrome of unilateral polymicrogyria affecting the right hemisphere. Neurology. 66: 133-5. PMID 16401865 DOI: 10.1212/01.wnl.0000191393.06679.e9 |
0.305 |
|
| 2006 |
Deuel TA, Liu JS, Corbo JC, Yoo SY, Rorke-Adams LB, Walsh CA. Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth. Neuron. 49: 41-53. PMID 16387638 DOI: 10.1016/J.Neuron.2005.10.038 |
0.803 |
|
| 2006 |
Lu J, Tiao G, Folkerth R, Hecht J, Walsh C, Sheen V. Overlapping expression of ARFGEF2 and Filamin A in the neuroependymal lining of the lateral ventricles: insights into the cause of periventricular heterotopia. The Journal of Comparative Neurology. 494: 476-84. PMID 16320251 DOI: 10.1002/Cne.20806 |
0.413 |
|
| 2006 |
Basel-Vanagaite L, Attia R, Yahav M, Ferland RJ, Anteki L, Walsh CA, Olender T, Straussberg R, Magal N, Taub E, Drasinover V, Alkelai A, Bercovich D, Rechavi G, Simon AJ, et al. The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation. Journal of Medical Genetics. 43: 203-10. PMID 16033914 DOI: 10.1136/Jmg.2005.035709 |
0.701 |
|
| 2005 |
Sheen VL, Walsh CA. Periventricular heterotopia: new insights into Ehlers-Danlos syndrome. Clinical Medicine & Research. 3: 229-33. PMID 16303888 DOI: 10.3121/Cmr.3.4.229 |
0.454 |
|
| 2005 |
Piao X, Chang BS, Bodell A, Woods K, Benzeev B, Topcu M, Guerrini R, Goldberg-Stern H, Sztriha L, Dobyns WB, Barkovich AJ, Walsh CA. Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes. Annals of Neurology. 58: 680-7. PMID 16240336 DOI: 10.1002/Ana.20616 |
0.447 |
|
| 2005 |
Shen J, Eyaid W, Mochida GH, Al-Moayyad F, Bodell A, Woods CG, Walsh CA. ASPM mutations identified in patients with primary microcephaly and seizures. Journal of Medical Genetics. 42: 725-9. PMID 16141009 DOI: 10.1136/Jmg.2004.027706 |
0.487 |
|
| 2005 |
Hill RS, Walsh CA. Molecular insights into human brain evolution. Nature. 437: 64-7. PMID 16136130 DOI: 10.1038/nature04103 |
0.315 |
|
| 2005 |
Ferland RJ, Li X, Buhlmann JE, Bu X, Walsh CA, Lim B. Characterization of Rho-GDIgamma and Rho-GDIalpha mRNA in the developing and mature brain with an analysis of mice with targeted deletions of Rho-GDIgamma. Brain Research. 1054: 9-21. PMID 16054116 DOI: 10.1016/J.Brainres.2005.04.088 |
0.677 |
|
| 2005 |
Kouprina N, Pavlicek A, Collins NK, Nakano M, Noskov VN, Ohzeki J, Mochida GH, Risinger JI, Goldsmith P, Gunsior M, Solomon G, Gersch W, Kim JH, Barrett JC, Walsh CA, et al. The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein. Human Molecular Genetics. 14: 2155-65. PMID 15972725 DOI: 10.1093/hmg/ddi220 |
0.396 |
|
| 2005 |
Soukoulis V, Reddy S, Pooley RD, Feng Y, Walsh CA, Bader DM. Cytoplasmic LEK1 is a regulator of microtubule function through its interaction with the LIS1 pathway. Proceedings of the National Academy of Sciences of the United States of America. 102: 8549-54. PMID 15939891 DOI: 10.1073/Pnas.0502303102 |
0.308 |
|
| 2005 |
van Reeuwijk J, Janssen M, van den Elzen C, Beltran-Valero de Bernabé D, Sabatelli P, Merlini L, Boon M, Scheffer H, Brockington M, Muntoni F, Huynen MA, Verrips A, Walsh CA, Barth PG, Brunner HG, et al. POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome. Journal of Medical Genetics. 42: 907-12. PMID 15894594 DOI: 10.1136/Jmg.2005.031963 |
0.426 |
|
| 2005 |
Sun T, Patoine C, Abu-Khalil A, Visvader J, Sum E, Cherry TJ, Orkin SH, Geschwind DH, Walsh CA. Early asymmetry of gene transcription in embryonic human left and right cerebral cortex. Science (New York, N.Y.). 308: 1794-8. PMID 15894532 DOI: 10.1126/Science.1110324 |
0.795 |
|
| 2005 |
Tietjen I, Erdogan F, Currier S, Apse K, Chang BS, Hill RS, Lee CK, Walsh CA. EMX2-independent familial schizencephaly: clinical and genetic analyses. American Journal of Medical Genetics. Part A. 135: 166-70. PMID 15887302 DOI: 10.1002/Ajmg.A.30734 |
0.811 |
|
| 2005 |
Shen J, Walsh CA. Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice. Molecular and Cellular Biology. 25: 3639-47. PMID 15831469 DOI: 10.1128/Mcb.25.9.3639-3647.2005 |
0.457 |
|
| 2005 |
Bond J, Roberts E, Springell K, Lizarraga SB, Lizarraga S, Scott S, Higgins J, Hampshire DJ, Morrison EE, Leal GF, Silva EO, Costa SM, Baralle D, Raponi M, Karbani G, ... ... Walsh CA, et al. A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Nature Genetics. 37: 353-5. PMID 15793586 DOI: 10.1038/ng1539 |
0.827 |
|
| 2005 |
Chang BS, Ly J, Appignani B, Bodell A, Apse KA, Ravenscroft RS, Sheen VL, Doherty MJ, Hackney DB, O'Connor M, Galaburda AM, Walsh CA. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology. 64: 799-803. PMID 15753412 DOI: 10.1212/01.Wnl.0000152874.57180.Af |
0.31 |
|
| 2005 |
Sheen VL, Jansen A, Chen MH, Parrini E, Morgan T, Ravenscroft R, Ganesh V, Underwood T, Wiley J, Leventer R, Vaid RR, Ruiz DE, Hutchins GM, Menasha J, Willner J, ... ... Walsh CA, et al. Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome. Neurology. 64: 254-62. PMID 15668422 DOI: 10.1212/01.Wnl.0000149512.79621.Df |
0.725 |
|
| 2005 |
Currier SC, Lee CK, Chang BS, Bodell AL, Pai GS, Job L, Lagae LG, Al-Gazali LI, Eyaid WM, Enns G, Dobyns WB, Walsh CA. Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndrome. American Journal of Medical Genetics. Part A. 133: 53-7. PMID 15637732 DOI: 10.1002/Ajmg.A.30487 |
0.812 |
|
| 2004 |
Imitola J, Raddassi K, Park KI, Mueller FJ, Nieto M, Teng YD, Frenkel D, Li J, Sidman RL, Walsh CA, Snyder EY, Khoury SJ. Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1alpha/CXC chemokine receptor 4 pathway. Proceedings of the National Academy of Sciences of the United States of America. 101: 18117-22. PMID 15608062 DOI: 10.1073/Pnas.0408258102 |
0.708 |
|
| 2004 |
Feng Y, Walsh CA. The many faces of filamin: a versatile molecular scaffold for cell motility and signalling. Nature Cell Biology. 6: 1034-8. PMID 15516996 DOI: 10.1038/ncb1104-1034 |
0.354 |
|
| 2004 |
Feng Y, Walsh CA. Mitotic spindle regulation by Nde1 controls cerebral cortical size. Neuron. 44: 279-93. PMID 15473967 DOI: 10.1016/j.neuron.2004.09.023 |
0.391 |
|
| 2004 |
Nieto M, Monuki ES, Tang H, Imitola J, Haubst N, Khoury SJ, Cunningham J, Gotz M, Walsh CA. Expression of Cux-1 and Cux-2 in the subventricular zone and upper layers II-IV of the cerebral cortex. The Journal of Comparative Neurology. 479: 168-80. PMID 15452856 DOI: 10.1002/Cne.20322 |
0.776 |
|
| 2004 |
Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, Walsh CA. Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome. Nature Genetics. 36: 1008-13. PMID 15322546 DOI: 10.1038/Ng1419 |
0.696 |
|
| 2004 |
Schuurmans C, Armant O, Nieto M, Stenman JM, Britz O, Klenin N, Brown C, Langevin LM, Seibt J, Tang H, Cunningham JM, Dyck R, Walsh C, Campbell K, Polleux F, et al. Sequential phases of cortical specification involve Neurogenin-dependent and -independent pathways. The Embo Journal. 23: 2892-902. PMID 15229646 DOI: 10.1038/Sj.Emboj.7600278 |
0.747 |
|
| 2004 |
Gaitanis JN, Walsh CA. Genetics of disorders of cortical development. Neuroimaging Clinics of North America. 14: 219-29, viii. PMID 15182816 DOI: 10.1016/j.nic.2004.03.007 |
0.378 |
|
| 2004 |
Mochida GH, Rajab A, Eyaid W, Lu A, Al-Nouri D, Kosaki K, Noruzinia M, Sarda P, Ishihara J, Bodell A, Apse K, Walsh CA. Broader geographical spectrum of Cohen syndrome due to COH1 mutations. Journal of Medical Genetics. 41: e87. PMID 15173253 DOI: 10.1136/Jmg.2003.014779 |
0.427 |
|
| 2004 |
Sheen VL, Basel-Vanagaite L, Goodman JR, Scheffer IE, Bodell A, Ganesh VS, Ravenscroft R, Hill RS, Cherry TJ, Shugart YY, Barkovich J, Straussberg R, Walsh CA. Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus. Brain & Development. 26: 326-34. PMID 15165674 DOI: 10.1016/J.Braindev.2003.09.004 |
0.821 |
|
| 2004 |
Chang BS, Piao X, Giannini C, Cascino GD, Scheffer I, Woods CG, Topcu M, Tezcan K, Bodell A, Leventer RJ, Barkovich AJ, Grant PE, Walsh CA. Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation. Neurology. 62: 1722-8. PMID 15159468 DOI: 10.1212/01.Wnl.0000125187.52952.E9 |
0.356 |
|
| 2004 |
Mochida GH, Walsh CA. Genetic basis of developmental malformations of the cerebral cortex. Archives of Neurology. 61: 637-40. PMID 15148137 DOI: 10.1001/archneur.61.5.637 |
0.44 |
|
| 2004 |
Kouprina N, Pavlicek A, Mochida GH, Solomon G, Gersch W, Yoon YH, Collura R, Ruvolo M, Barrett JC, Woods CG, Walsh CA, Jurka J, Larionov V. Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion. Plos Biology. 2: E126. PMID 15045028 DOI: 10.1371/Journal.Pbio.0020126 |
0.419 |
|
| 2004 |
Piao X, Hill RS, Bodell A, Chang BS, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Ross ME, Michaud JL, Déscarie JC, Barkovich AJ, ... Walsh CA, et al. G protein-coupled receptor-dependent development of human frontal cortex. Science (New York, N.Y.). 303: 2033-6. PMID 15044805 DOI: 10.1126/Science.1092780 |
0.371 |
|
| 2004 |
Chae TH, Kim S, Marz KE, Hanson PI, Walsh CA. The hyh mutation uncovers roles for alpha Snap in apical protein localization and control of neural cell fate. Nature Genetics. 36: 264-70. PMID 14758363 DOI: 10.1038/Ng1302 |
0.816 |
|
| 2004 |
Basel-Vanagaite L, Straussberg R, Ovadia H, Kaplan A, Magal N, Shorer Z, Shalev H, Walsh C, Shohat M. Infantile bilateral striatal necrosis maps to chromosome 19q Neurology. 62: 87-90. PMID 14718703 DOI: 10.1212/01.Wnl.0000101680.49036.69 |
0.346 |
|
| 2004 |
Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA. Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex. Nature Genetics. 36: 69-76. PMID 14647276 DOI: 10.1038/Ng1276 |
0.751 |
|
| 2004 |
Jansen JH, Feng Y, Lee B, Massop M, De Witte T, Williams I, Gilliland G, Walsh C, van der Reijden BA. Disruption of the NDE1 Gene Occurs in 90% of the Cases of inv(16) AML and Results in Chromosomal Instability and Myeloproliferative Disease in Mice. Blood. 104: 61-61. DOI: 10.1182/blood.v104.11.61.61 |
0.348 |
|
| 2004 |
Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, Walsh CA. Erratum: Corrigendum: Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome Nature Genetics. 36: 1126-1126. DOI: 10.1038/Ng1004-1126B |
0.673 |
|
| 2004 |
Chae TH, Kim S, Marz KE, Hanson PI, Walsh CA. Erratum: Corrigendum: The hyh mutation uncovers roles for αSnap in apical protein localization and control of neural cell fate Nature Genetics. 36: 427-427. DOI: 10.1038/Ng0404-427C |
0.8 |
|
| 2003 |
Chang BS, Walsh CA. Mapping form and function in the human brain: the emerging field of functional neuroimaging in cortical malformations. Epilepsy & Behavior : E&B. 4: 618-25. PMID 14698694 DOI: 10.1016/J.Yebeh.2003.09.006 |
0.358 |
|
| 2003 |
Bond J, Scott S, Hampshire DJ, Springell K, Corry P, Abramowicz MJ, Mochida GH, Hennekam RC, Maher ER, Fryns JP, Alswaid A, Jafri H, Rashid Y, Mubaidin A, Walsh CA, et al. Protein-truncating mutations in ASPM cause variable reduction in brain size. American Journal of Human Genetics. 73: 1170-7. PMID 14574646 DOI: 10.1086/379085 |
0.447 |
|
| 2003 |
Sheen VL, Walsh CA. Developmental genetic malformations of the cerebral cortex. Current Neurology and Neuroscience Reports. 3: 433-41. PMID 12914687 DOI: 10.1007/S11910-003-0027-8 |
0.395 |
|
| 2003 |
Rajab A, Mochida GH, Hill A, Ganesh V, Bodell A, Riaz A, Grant PE, Shugart YY, Walsh CA. A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Neurology. 60: 1664-7. PMID 12771259 DOI: 10.1212/01.Wnl.0000068548.58498.41 |
0.753 |
|
| 2003 |
Chenn A, Walsh CA. Increased neuronal production, enlarged forebrains and cytoarchitectural distortions in beta-catenin overexpressing transgenic mice. Cerebral Cortex (New York, N.Y. : 1991). 13: 599-606. PMID 12764034 DOI: 10.1093/cercor/13.6.599 |
0.691 |
|
| 2003 |
Lee A, Maldonado M, Baybis M, Walsh CA, Scheithauer B, Yeung R, Parent J, Weiner HL, Crino PB. Markers of cellular proliferation are expressed in cortical tubers. Annals of Neurology. 53: 668-73. PMID 12731003 DOI: 10.1002/Ana.10579 |
0.328 |
|
| 2003 |
Chang BS, Piao X, Bodell A, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Grant PE, Barkovich AJ, Walsh CA. Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. Annals of Neurology. 53: 596-606. PMID 12730993 DOI: 10.1002/Ana.10520 |
0.35 |
|
| 2003 |
Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. The Journal of Comparative Neurology. 460: 266-79. PMID 12687690 DOI: 10.1002/Cne.10654 |
0.812 |
|
| 2003 |
Sheen VL, Topçu M, Berkovic S, Yalnizoglu D, Blatt I, Bodell A, Hill RS, Ganesh VS, Cherry TJ, Shugart YY, Walsh CA. Autosomal recessive form of periventricular heterotopia. Neurology. 60: 1108-12. PMID 12682315 DOI: 10.1212/01.Wnl.0000055898.00349.02 |
0.807 |
|
| 2003 |
Zollino M, Colosimo C, Zuffardi O, Rossi E, Tosolini A, Walsh CA, Neri G. Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X-linked trait. American Journal of Medical Genetics. Part A. 117: 65-71. PMID 12548742 DOI: 10.1002/ajmg.a.10068 |
0.313 |
|
| 2002 |
Kakita A, Hayashi S, Moro F, Guerrini R, Ozawa T, Ono K, Kameyama S, Walsh CA, Takahashi H. Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex. Acta Neuropathologica. 104: 649-57. PMID 12410386 DOI: 10.1007/s00401-002-0594-9 |
0.385 |
|
| 2002 |
Sheen VL, Feng Y, Graham D, Takafuta T, Shapiro SS, Walsh CA. Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact. Human Molecular Genetics. 11: 2845-54. PMID 12393796 DOI: 10.1093/Hmg/11.23.2845 |
0.405 |
|
| 2002 |
Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, Celli J, van Beusekom E, van der Zwaag B, Kayserili H, Merlini L, Chitayat D, Dobyns WB, Cormand B, Lehesjoki AE, Cruces J, Voit T, Walsh CA, et al. Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. American Journal of Human Genetics. 71: 1033-43. PMID 12369018 DOI: 10.1086/342975 |
0.83 |
|
| 2002 |
Bond J, Roberts E, Mochida GH, Hampshire DJ, Scott S, Askham JM, Springell K, Mahadevan M, Crow YJ, Markham AF, Walsh CA, Woods CG. ASPM is a major determinant of cerebral cortical size. Nature Genetics. 32: 316-20. PMID 12355089 DOI: 10.1038/ng995 |
0.45 |
|
| 2002 |
Corbo JC, Deuel TA, Long JM, LaPorte P, Tsai E, Wynshaw-Boris A, Walsh CA. Doublecortin is required in mice for lamination of the hippocampus but not the neocortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 7548-57. PMID 12196578 DOI: 10.1523/Jneurosci.22-17-07548.2002 |
0.817 |
|
| 2002 |
Chenn A, Walsh CA. Regulation of cerebral cortical size by control of cell cycle exit in neural precursors. Science (New York, N.Y.). 297: 365-9. PMID 12130776 DOI: 10.1126/science.1074192 |
0.691 |
|
| 2002 |
Olson EC, Walsh CA. Smooth, rough and upside-down neocortical development. Current Opinion in Genetics & Development. 12: 320-7. PMID 12076676 DOI: 10.1016/S0959-437X(02)00305-2 |
0.464 |
|
| 2002 |
Reid CB, Walsh CA. Evidence of common progenitors and patterns of dispersion in rat striatum and cerebral cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 4002-14. PMID 12019320 DOI: 10.1523/Jneurosci.22-10-04002.2002 |
0.334 |
|
| 2002 |
Chae TH, Allen KM, Davisson MT, Sweet HO, Walsh CA. Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 239-44. PMID 12016511 DOI: 10.1007/s00335-001-2144-5 |
0.794 |
|
| 2002 |
Piao X, Basel-Vanagaite L, Straussberg R, Grant PE, Pugh EW, Doheny K, Doan B, Hong SE, Shugart YY, Walsh CA. An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. American Journal of Human Genetics. 70: 1028-33. PMID 11845408 DOI: 10.1086/339552 |
0.411 |
|
| 2001 |
Monuki ES, Porter FD, Walsh CA. Patterning of the dorsal telencephalon and cerebral cortex by a roof plate-Lhx2 pathway. Neuron. 32: 591-604. PMID 11719201 DOI: 10.1016/S0896-6273(01)00504-9 |
0.636 |
|
| 2001 |
Monuki ES, Walsh CA. Mechanisms of cerebral cortical patterning in mice and humans. Nature Neuroscience. 4: 1199-206. PMID 11687830 DOI: 10.1038/nn752 |
0.637 |
|
| 2001 |
Sheen VL, Dixon PH, Fox JW, Hong SE, Kinton L, Sisodiya SM, Duncan JS, Dubeau F, Scheffer IE, Schachter SC, Wilner A, Henchy R, Crino P, Kamuro K, DiMario F, ... ... Walsh CA, et al. Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Human Molecular Genetics. 10: 1775-83. PMID 11532987 DOI: 10.1093/Hmg/10.17.1775 |
0.395 |
|
| 2001 |
Ross ME, Walsh CA. Human brain malformations and their lessons for neuronal migration. Annual Review of Neuroscience. 24: 1041-70. PMID 11520927 DOI: 10.1146/annurev.neuro.24.1.1041 |
0.4 |
|
| 2001 |
Feng Y, Walsh CA. Protein-protein interactions, cytoskeletal regulation and neuronal migration. Nature Reviews. Neuroscience. 2: 408-16. PMID 11389474 DOI: 10.1038/35077559 |
0.428 |
|
| 2001 |
Mochida GH, Walsh CA. Molecular genetics of human microcephaly. Current Opinion in Neurology. 14: 151-6. PMID 11262728 DOI: 10.1097/00019052-200104000-00003 |
0.397 |
|
| 2001 |
McCarthy M, Turnbull DH, Walsh CA, Fishell G. Telencephalic Neural Progenitors Appear To Be Restricted to Regional and Glial Fates before the Onset of Neurogenesis The Journal of Neuroscience. 21: 6772-6781. DOI: 10.1523/Jneurosci.21-17-06772.2001 |
0.334 |
|
| 2000 |
Feng Y, Olson EC, Stukenberg PT, Flanagan LA, Kirschner MW, Walsh CA. LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome. Neuron. 28: 665-79. PMID 11163258 DOI: 10.1016/S0896-6273(00)00145-8 |
0.363 |
|
| 2000 |
Lin PT, Gleeson JG, Corbo JC, Flanagan L, Walsh CA. DCAMKL1 encodes a protein kinase with homology to doublecortin that regulates microtubule polymerization. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 9152-61. PMID 11124993 DOI: 10.1523/Jneurosci.20-24-09152.2000 |
0.788 |
|
| 2000 |
Schwartzkroin PA, Walsh CA. Cortical malformations and epilepsy. Mental Retardation and Developmental Disabilities Research Reviews. 6: 268-80. PMID 11107192 DOI: 10.1002/1098-2779(2000)6:4<268::Aid-Mrdd6>3.0.Co;2-B |
0.438 |
|
| 2000 |
Poussaint TY, Fox JW, Dobyns WB, Radtke R, Scheffer IE, Berkovic SF, Barnes PD, Huttenlocher PR, Walsh CA. Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings. Pediatric Radiology. 30: 748-55. PMID 11100490 DOI: 10.1007/S002470000312 |
0.423 |
|
| 2000 |
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nature Genetics. 26: 93-6. PMID 10973257 DOI: 10.1038/79246 |
0.504 |
|
| 2000 |
Bienvenu T, des Portes V, McDonell N, Carrié A, Zemni R, Couvert P, Ropers HH, Moraine C, van Bokhoven H, Fryns JP, Allen K, Walsh CA, Boué J, Kahn A, Chelly J, et al. Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation. American Journal of Medical Genetics. 93: 294-8. PMID 10946356 DOI: 10.1002/1096-8628(20000814)93:4<294::AID-AJMG8>3.0.CO;2-F |
0.43 |
|
| 2000 |
Taylor KR, Holzer AK, Bazan JF, Walsh CA, Gleeson JG. Patient mutations in doublecortin define a repeated tubulin-binding domain. The Journal of Biological Chemistry. 275: 34442-50. PMID 10946000 DOI: 10.1074/Jbc.M007078200 |
0.569 |
|
| 2000 |
Dulabon L, Olson EC, Taglienti MG, Eisenhuth S, McGrath B, Walsh CA, Kreidberg JA, Anton ES. Reelin binds alpha3beta1 integrin and inhibits neuronal migration. Neuron. 27: 33-44. PMID 10939329 DOI: 10.1016/S0896-6273(00)00007-6 |
0.361 |
|
| 2000 |
Gleeson JG, Minnerath S, Kuzniecky RI, Dobyns WB, Young ID, Ross ME, Walsh CA. Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes. American Journal of Human Genetics. 67: 574-81. PMID 10915612 DOI: 10.1086/303043 |
0.58 |
|
| 2000 |
Gleeson JG, Walsh CA. Neuronal migration disorders: from genetic diseases to developmental mechanisms. Trends in Neurosciences. 23: 352-9. PMID 10906798 DOI: 10.1016/S0166-2236(00)01607-6 |
0.581 |
|
| 2000 |
Walsh CA. Genetics of neuronal migration in the cerebral cortex. Mental Retardation and Developmental Disabilities Research Reviews. 6: 34-40. PMID 10899795 DOI: 10.1002/(SICI)1098-2779(2000)6:1<34::AID-MRDD5>3.0.CO;2-Y |
0.476 |
|
| 2000 |
Monuki ES, Walsh CA. Proto-mapping the areas of cerebral cortex: transcription factors make the grade. Nature Neuroscience. 3: 640-1. PMID 10862691 DOI: 10.1038/76587 |
0.619 |
|
| 2000 |
Walsh CA, Goffinet AM. Potential mechanisms of mutations that affect neuronal migration in man and mouse. Current Opinion in Genetics & Development. 10: 270-4. PMID 10826984 DOI: 10.1016/S0959-437X(00)00076-9 |
0.456 |
|
| 2000 |
Gleeson JG, Luo RF, Grant PE, Guerrini R, Huttenlocher PR, Berg MJ, Ricci S, Cusmai R, Wheless JW, Berkovic S, Scheffer I, Dobyns WB, Walsh CA. Genetic and neuroradiological heterogeneity of double cortex syndrome. Annals of Neurology. 47: 265-9. PMID 10665503 DOI: 10.1002/1531-8249(200002)47:2<265::Aid-Ana22>3.0.Co;2-N |
0.588 |
|
| 1999 |
Illarioshkin SN, Allen KM, Gleeson JG, Tsuji S, Ikeuchi T, Markova ED, Walsh CA, Ivanova-Smolenskaya IA. Studies of the candidate genes in X-linked congenital cerebellar hypoplasia. Journal of Neurology. 246: 1177-80. PMID 10653312 DOI: 10.1007/S004150050539 |
0.576 |
|
| 1999 |
Chenn A, Walsh CA. Perspectives: neurobiology. Cranking it up a notch. Science (New York, N.Y.). 286: 689-90. PMID 10577225 DOI: 10.1126/science.286.5440.689 |
0.672 |
|
| 1999 |
Allen KM, Walsh CA. Genes that regulate neuronal migration in the cerebral cortex Epilepsy Research. 36: 143-154. PMID 10515162 DOI: 10.1016/S0920-1211(99)00048-0 |
0.448 |
|
| 1999 |
Ware ML, Tavazoie SF, Reid CB, Walsh CA. Coexistence of widespread clones and large radial clones in early embryonic ferret cortex. Cerebral Cortex (New York, N.Y. : 1991). 9: 636-45. PMID 10498282 DOI: 10.1093/cercor/9.6.636 |
0.332 |
|
| 1999 |
Dobyns WB, Truwit CL, Ross ME, Matsumoto N, Pilz DT, Ledbetter DH, Gleeson JG, Walsh CA, Barkovich AJ. Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly. Neurology. 53: 270-7. PMID 10430413 DOI: 10.1212/Wnl.53.2.270 |
0.614 |
|
| 1999 |
Gleeson JG, Lin PT, Flanagan LA, Walsh CA. Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons. Neuron. 23: 257-71. PMID 10399933 DOI: 10.1016/S0896-6273(00)80778-3 |
0.683 |
|
| 1999 |
Fox JW, Walsh CA. Periventricular heterotopia and the genetics of neuronal migration in the cerebral cortex. American Journal of Human Genetics. 65: 19-24. PMID 10364512 DOI: 10.1086/302474 |
0.39 |
|
| 1999 |
Reid CB, Liang I, Walsh CA. Clonal mixing, clonal restriction, and specification of cell types in the developing rat olfactory bulb. The Journal of Comparative Neurology. 403: 106-18. PMID 10075446 DOI: 10.1002/(SICI)1096-9861(19990105)403:1<106::AID-CNE8>3.0.CO;2-S |
0.311 |
|
| 1999 |
Gleeson JG, Minnerath SR, Fox JW, Allen KM, Luo RF, Hong SE, Berg MJ, Kuzniecky R, Reitnauer PJ, Borgatti R, Mira AP, Guerrini R, Holmes GL, Rooney CM, Berkovic S, ... ... Walsh CA, et al. Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. Annals of Neurology. 45: 146-53. PMID 9989615 DOI: 10.1002/1531-8249(199902)45:2<146::Aid-Ana3>3.0.Co;2-N |
0.58 |
|
| 1999 |
Fox JW, Lamperti ED, Ekşioğlu YZ, Hong SE, Feng Y, Graham DA, Scheffer IE, Dobyns WB, Hirsch BA, Radtke RA, Berkovic SF, Huttenlocher PR, Walsh CA. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron. 21: 1315-25. PMID 9883725 DOI: 10.1016/S0896-6273(00)80651-0 |
0.42 |
|
| 1998 |
Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Human Molecular Genetics. 7: 2029-37. PMID 9817918 DOI: 10.1093/Hmg/7.13.2029 |
0.617 |
|
| 1998 |
Allen KM, Gleeson JG, Shoup SM, Walsh CA. A YAC contig in Xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3. Genomics. 52: 214-8. PMID 9782089 DOI: 10.1006/Geno.1998.5424 |
0.543 |
|
| 1998 |
Allen KM, Gleeson JG, Bagrodia S, Partington MW, MacMillan JC, Cerione RA, Mulley JC, Walsh CA. PAK3 mutation in nonsyndromic X-linked mental retardation. Nature Genetics. 20: 25-30. PMID 9731525 DOI: 10.1038/1675 |
0.62 |
|
| 1998 |
Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell. 92: 63-72. PMID 9489700 DOI: 10.1016/S0092-8674(00)80899-5 |
0.617 |
|
| 1997 |
Walsh CA, Bowler WB, Bilbe G, Fraser WD, Gallagher JA. Effects of PTH on PTHrP gene expression in human osteoblasts: up-regulation with the kinetics of an immediate early gene. Biochemical and Biophysical Research Communications. 239: 155-9. PMID 9345287 DOI: 10.1006/Bbrc.1997.7351 |
0.315 |
|
| 1997 |
Ware ML, Fox JW, González JL, Davis NM, Lambert de Rouvroit C, Russo CJ, Chua SC, Goffinet AM, Walsh CA. Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse. Neuron. 19: 239-49. PMID 9292716 DOI: 10.1016/S0896-6273(00)80936-8 |
0.446 |
|
| 1997 |
Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, Harding BN, Andermann E, Abdullah R, Berg M, Czapansky-Bielman D, Flanders DJ, Guerrini R, Motté J, Mira AP, ... ... Walsh CA, et al. Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain. Human Molecular Genetics. 6: 555-62. PMID 9097958 DOI: 10.1093/Hmg/6.4.555 |
0.595 |
|
| 1997 |
Reid CB, Walsh CA. Early development of the cerebral cortex. Progress in Brain Research. 108: 17-30. PMID 8979791 DOI: 10.1016/S0079-6123(08)62529-7 |
0.336 |
|
| 1997 |
González JL, Russo CJ, Goldowitz D, Sweet HO, Davisson MT, Walsh CA. Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype The Journal of Neuroscience. 17: 9204-9211. DOI: 10.1523/Jneurosci.17-23-09204.1997 |
0.436 |
|
| 1996 |
Walsh CA. Neural development: identical twins separated at birth? Current Biology : Cb. 6: 26-8. PMID 8805214 DOI: 10.1016/S0960-9822(02)00413-X |
0.352 |
|
| 1996 |
Dobyns WB, Andermann E, Andermann F, Czapansky-Beilman D, Dubeau F, Dulac O, Guerrini R, Hirsch B, Ledbetter DH, Lee NS, Motte J, Pinard JM, Radtke RA, Ross ME, Tampieri D, ... Walsh CA, et al. X-linked malformations of neuronal migration. Neurology. 47: 331-9. PMID 8757001 DOI: 10.1212/Wnl.47.2.331 |
0.379 |
|
| 1996 |
Ekşioğlu YZ, Scheffer IE, Cardenas P, Knoll J, DiMario F, Ramsby G, Berg M, Kamuro K, Berkovic SF, Duyk GM, Parisi J, Huttenlocher PR, Walsh CA. Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical development. Neuron. 16: 77-87. PMID 8562093 DOI: 10.1016/S0896-6273(00)80025-2 |
0.346 |
|
| 1995 |
Reid CB, Liang I, Walsh C. Systematic widespread clonal organization in cerebral cortex. Neuron. 15: 299-310. PMID 7646887 DOI: 10.1016/0896-6273(95)90035-7 |
0.32 |
|
| 1994 |
Goodman S, Xiao X, Donahue R, Moulton A, Miller J, Walsh C, Young N, Samulski R, Nienhuis A. Recombinant adeno-associated virus-mediated gene transfer into hematopoietic progenitor cells [published erratum appears in Blood 1995 Feb 1;85(3):862] Blood. 84: 1492-1500. DOI: 10.1182/Blood.V84.5.1492.Bloodjournal8451492 |
0.319 |
|
| 1993 |
Walsh C, Cepko CL. Clonal dispersion in proliferative layers of developing cerebral cortex. Nature. 362: 632-5. PMID 8464513 DOI: 10.1038/362632a0 |
0.651 |
|
| 1993 |
Cepko CL, Ryder EF, Austin CP, Walsh C, Fekete DM. Lineage analysis using retrovirus vectors. Methods in Enzymology. 225: 933-60. PMID 8231895 DOI: 10.1016/0076-6879(93)25059-B |
0.702 |
|
| 1992 |
Walsh C, Cepko CL. Widespread dispersion of neuronal clones across functional regions of the cerebral cortex. Science (New York, N.Y.). 255: 434-40. PMID 1734520 DOI: 10.1126/Science.1734520 |
0.697 |
|
| 1992 |
Snyder EY, Deitcher DL, Walsh C, Arnold-Aldea S, Hartwieg EA, Cepko CL. Multipotent neural cell lines can engraft and participate in development of mouse cerebellum. Cell. 68: 33-51. PMID 1732063 DOI: 10.1016/0092-8674(92)90204-P |
0.733 |
|
| 1990 |
Cepko CL, Austin CP, Walsh C, Ryder EF, Halliday A, Fields-Berry S. Studies of cortical development using retrovirus vectors. Cold Spring Harbor Symposia On Quantitative Biology. 55: 265-78. PMID 2132820 DOI: 10.1101/Sqb.1990.055.01.029 |
0.702 |
|
| 1988 |
Walsh C, Cepko CL. Clonally related cortical cells show several migration patterns. Science (New York, N.Y.). 241: 1342-5. PMID 3137660 DOI: 10.1126/SCIENCE.3137660 |
0.682 |
|
| 1987 |
Guillery RW, Walsh C. Early uncrossed component of the developing optic nerve with a short extracerebral course: a light and electron microscopic study of fetal ferrets. The Journal of Comparative Neurology. 265: 218-23. PMID 3693607 DOI: 10.1002/cne.902650206 |
0.505 |
|
| 1987 |
Guillery RW, Walsh C. Changing glial organization relates to changing fiber order in the developing optic nerve of ferrets. The Journal of Comparative Neurology. 265: 203-17. PMID 3693606 DOI: 10.1002/cne.902650205 |
0.523 |
|
| 1984 |
Walsh C, Guillery RW. Fibre order in the pathways from the eye to the brain Trends in Neurosciences. 7: 208,209-211. DOI: 10.1016/S0166-2236(84)80012-0 |
0.534 |
|
| 1983 |
Walsh C, Polley EH, Hickey TL, Guillery RW. Generation of cat retinal ganglion cells in relation to central pathways. Nature. 302: 611-4. PMID 6835394 DOI: 10.1038/302611a0 |
0.541 |
|
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