Chris A. Walsh - Publications

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
Genes involved in the development and function of the cerebral cortex
Website:
http://www.walshlab.org/

296 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.388
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  0.335
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  0.775
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  0.703
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  0.798
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  0.352
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  0.461
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  0.8
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  0.418
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  0.483
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  0.389
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  0.756
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  0.588
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  0.39
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  0.795
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  0.686
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  0.406
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  0.4
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  0.815
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  0.75
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  0.795
2018 Rodin RE, Walsh CA. Somatic Mutation in Pediatric Neurological Diseases. Pediatric Neurology. PMID 30249355 DOI: 10.1016/j.pediatrneurol.2018.08.008  0.45
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  0.305
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  0.362
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  0.806
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  0.347
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  0.313
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  0.572
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  0.426
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  0.327
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  0.754
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  0.838
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  0.689
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  0.748
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  0.826
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  0.428
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  0.823
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  0.618
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  0.805
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  0.576
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  0.793
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  0.724
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  0.789
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  0.8
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  0.823
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  0.803
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  0.827
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  0.413
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  0.826
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  0.8
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  0.611
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  0.393
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  0.437
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  0.733
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  0.743
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  0.347
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  0.806
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  0.625
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  0.773
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  0.821
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  0.569
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  0.766
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  0.73
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  0.778
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  0.791
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  0.829
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  0.801
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  0.808
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  0.612
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  0.314
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  0.436
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  0.789
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  0.751
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  0.75
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  0.418
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  0.331
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  0.774
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  0.808
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  0.801
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  0.826
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  0.661
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  0.399
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  0.34
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  0.738
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  0.803
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  0.769
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  0.737
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  0.343
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  0.666
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  0.799
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  0.788
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  0.335
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  0.739
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  0.389
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  0.796
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  0.426
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  0.419
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  0.719
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  0.446
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  0.684
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  0.77
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  0.814
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  0.773
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  0.392
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  0.34
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  0.323
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  0.79
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  0.495
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  0.347
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  0.475
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  0.604
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  0.641
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  0.359
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  0.679
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  0.625
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  0.467
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  0.418
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 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  0.709
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  0.415
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  0.743
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  0.675
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  0.821
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  0.832
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  0.402
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  0.43
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  0.816
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  0.714
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  0.548
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  0.69
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  0.746
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  0.817
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  0.358
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  0.445
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  0.78
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  0.359
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  0.398
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  0.383
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  0.44
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  0.644
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  0.579
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  0.707
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  0.493
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  0.408
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  0.337
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  0.622
2006 Sun T, Walsh CA. Molecular approaches to brain asymmetry and handedness. Nature Reviews. Neuroscience. 7: 655-62. PMID 16858393 DOI: 10.1038/nrn1930  0.402
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  0.669
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  0.437
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  0.47
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  0.527
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  0.69
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  0.448
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  0.662
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  0.691
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  0.351
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  0.813
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  0.716
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  0.411
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  0.449
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  0.498
2005 Hill RS, Walsh CA. Molecular insights into human brain evolution. Nature. 437: 64-7. PMID 16136130 DOI: 10.1038/nature04103  0.318
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  0.678
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  0.395
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  0.306
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  0.427
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  0.794
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  0.812
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  0.464
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  0.775
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  0.813
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  0.72
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  0.353
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  0.386
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  0.787
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  0.697
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  0.756
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  0.375
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  0.429
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  0.82
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  0.354
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  0.436
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  0.367
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  0.815
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  0.794
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  0.347
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  0.675
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  0.801
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  0.356
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  0.451
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  0.39
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  0.79
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  0.693
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  0.326
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  0.349
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  0.806
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  0.382
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  0.402
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  0.831
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  0.445
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  0.693
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  0.463
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  0.331
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  0.409
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  0.607
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  0.607
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  0.398
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  0.398
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  0.393
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  0.331
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  0.437
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  0.579
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  0.591
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  0.588
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  0.607
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  0.599
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  0.585
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  0.675
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  0.443
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  0.625
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  0.69
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  0.592
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  0.628
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  0.552
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  0.628
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  0.624
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  0.314
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  0.443
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  0.603
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  0.378
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  0.345
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  0.653
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  0.706
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  0.698
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  0.735
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  0.704
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  0.683
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  0.522
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  0.535
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  0.54
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