Chris A. Walsh - Publications

Harvard University, Cambridge, MA, United States 
Genes involved in the development and function of the cerebral cortex

308 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 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  0.72
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  0.6
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  0.6
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  0.72
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  0.4
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  0.72
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  0.6
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  0.6
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  0.6
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  0.72
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  0.72
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  0.56
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  0.6
2018 Rodin RE, Walsh CA. Somatic Mutation in Pediatric Neurological Diseases. Pediatric Neurology. PMID 30249355 DOI: 10.1016/j.pediatrneurol.2018.08.008  0.4
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  1
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  1
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  0.6
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  1
2018 Chen MH, Choudhury S, Hirata M, Khalsa S, Chang B, Walsh CA. Cover Image, Volume 176A, Number 2, February 2018. American Journal of Medical Genetics. Part A. 176: i. PMID 29334595 DOI: 10.1002/ajmg.a.38607  0.4
2018 Chen MH, Choudhury S, Hirata M, Khalsa S, Chang B, Walsh CA. Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations. American Journal of Medical Genetics. Part A. 176: 337-350. PMID 29334594 DOI: 10.1002/ajmg.a.38580  0.4
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  0.8
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  0.8
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  0.72
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  1
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  0.6
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  1
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  0.72
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  0.8
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  1
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  0.92
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  0.72
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2015 O'Leary BD, Walsh CA, Fitzgerald JM, Downey P, McAuliffe FM. The contribution of massive fetomaternal hemorrhage to antepartum stillbirth: a 25-year cross-sectional study. Acta Obstetricia Et Gynecologica Scandinavica. PMID 26332994 DOI: 10.1111/aogs.12762  0.4
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  1
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  1
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  0.72
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  1
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  1
2015 Walsh CA, Wilkinson M, Downey P, Mooney EE, Carroll S. "False" lambda sign in a monochorionic twin pregnancy. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. PMID 25708185 DOI: 10.1002/uog.14827  0.4
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  1
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  1
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  1
2015 Ghosh RM, Gates GJ, Walsh CA, Schiller MS, Pass RH, Ceresnak SR. The prevalence of arrhythmias, predictors for arrhythmias, and safety of exercise stress testing in children. Pediatric Cardiology. 36: 584-90. PMID 25384613 DOI: 10.1007/S00246-014-1053-9  0.36
2015 Barry SC, Walsh CA, Burke AL, McParland P, McAuliffe FM, Morrison JJ. Natural history of fetal trisomy 13 after prenatal diagnosis. American Journal of Medical Genetics. Part A. 167: 147-50. PMID 25339456 DOI: 10.1002/ajmg.a.36824  0.4
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  1
2014 Hidayatallah N, Silverstein LB, Stolerman M, McDonald T, Walsh CA, Paljevic E, Cohen LL, Marion RW, Wasserman D, Hreyo S, Dolan SM. Psychological stress associated with cardiogenetic conditions. Personalized Medicine. 11: 631-640. PMID 25431604 DOI: 10.2217/PME.14.50  0.36
2014 Jamuar SS, Walsh CA. Somatic mutations in cerebral cortical malformations. The New England Journal of Medicine. 371: 2038. PMID 25409382 DOI: 10.1056/NEJMc1411784  0.6
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  0.4
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  1
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  1
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  1
2014 Silverstein LB, Stolerman M, Hidayatallah N, McDonald T, Walsh CA, Paljevic E, Cohen LL, Marion RW, Wasserman D, Dolan SM. Translating advances in cardiogenetics into effective clinical practice. Qualitative Health Research. 24: 1315-28. PMID 25114027 DOI: 10.1177/1049732314546754  0.36
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  1
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  1
2014 Walsh CA, MacTiernan A, Farrell S, Mulcahy C, McMahon CJ, Franklin O, Coleman D, Mahony R, Higgins S, Carroll S, McParland P, McAuliffe FM. Mode of delivery in pregnancies complicated by major fetal congenital heart disease: a retrospective cohort study. Journal of Perinatology : Official Journal of the California Perinatal Association. 34: 901-5. PMID 24875409 DOI: 10.1038/jp.2014.104  0.4
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  1
2014 Walsh CA, Doyle B, Quigley J, McAuliffe FM, Fitzgerald J, Mahony R, Higgins S, Carroll S, McParland P. Reassessing critical maternal antibody threshold in RhD alloimmunization: a 16-year retrospective cohort study. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 44: 669-73. PMID 24706487 DOI: 10.1002/uog.13383  0.4
2014 Erskine KE, Hidayatallah NZ, Walsh CA, McDonald TV, Cohen L, Marion RW, Dolan SM. Motivation to pursue genetic testing in individuals with a personal or family history of cardiac events or sudden cardiac death. Journal of Genetic Counseling. 23: 849-59. PMID 24664857 DOI: 10.1007/s10897-014-9707-6  0.36
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  1
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  1
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  1
2014 O'Neill HA, Egan G, Walsh CA, Cotter AM, Walsh SR. Omission of the bladder flap at caesarean section reduces delivery time without increased morbidity: a meta-analysis of randomised controlled trials. European Journal of Obstetrics, Gynecology, and Reproductive Biology. 174: 20-6. PMID 24411951 DOI: 10.1016/j.ejogrb.2013.12.020  0.4
2014 Poduri A, Salih M, Walsh CA. Reply: To PMID 24243345. Annals of Neurology. 75: 326. PMID 24242934 DOI: 10.1002/ana.24055  1
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  1
2014 Mochida GH, Poduri A, Walsh CA. Genetic Disorders of Cerebral Cortical Development Reference Module in Biomedical Research. DOI: 10.1016/B978-0-12-801238-3.05587-2  1
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  1
2013 Walsh CA, McAuliffe F, Kinsella V, McParland P. Routine obstetric ultrasound services. Irish Medical Journal. 106: 311-3. PMID 24579412  0.4
2013 Erskine KE, Griffith E, Degroat N, Stolerman M, Silverstein LB, Hidayatallah N, Wasserman D, Paljevic E, Cohen L, Walsh CA, McDonald T, Marion RW, Dolan SM. An interdisciplinary approach to personalized medicine: case studies from a cardiogenetics clinic. Personalized Medicine. 10: 73-80. PMID 24496296 DOI: 10.2217/pme.12.108  0.36
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  1
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  1
2013 Walsh CA, Russell N, McAuliffe FM, Higgins S, Mahony R, Carroll S, McParland P. Relationship between maternal antibody type and antenatal course following intrauterine transfusion for red cell alloimmunisation. European Journal of Obstetrics, Gynecology, and Reproductive Biology. 171: 235-9. PMID 24075591 DOI: 10.1016/j.ejogrb.2013.09.002  0.4
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  1
2013 Healy DA, Walsh CA, Walsh SR. Suprapubic versus transurethral bladder catheterization following pelvic surgery. Current Opinion in Obstetrics & Gynecology. 25: 410-3. PMID 24018878 DOI: 10.1097/GCO.0b013e3283648d12  0.4
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  1
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  1
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  1
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  1
2013 Walsh CA, McAuliffe FM, Turowski G, Roald B, Mooney EE. A survey of obstetricians' views on placental pathology reporting. International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics. 121: 275-7. PMID 23490426 DOI: 10.1016/j.ijgo.2013.01.008  0.4
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  1
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  1
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  1
2013 Walsh CA, Robson M, McAuliffe FM. Mode of delivery at term and adverse neonatal outcomes. Obstetrics and Gynecology. 121: 122-8. PMID 23262936 DOI: http://10.1097/AOG.0b013e3182749ac9  0.4
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  1
2013 Lindsay KL, Walsh CA, Brennan L, McAuliffe FM. Probiotics in pregnancy and maternal outcomes: a systematic review. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 26: 772-8. PMID 23205866 DOI: 10.3109/14767058.2012.755166  0.4
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  1
2013 Walsh CA, Cheng Y, Mansfield KJ, Parkin K, Mukerjee C, Moore KH. Decreased intravesical adenosine triphosphate in patients with refractory detrusor overactivity and bacteriuria. The Journal of Urology. 189: 1383-7. PMID 23063632 DOI: 10.1016/j.juro.2012.10.003  0.4
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  1
2012 Walsh CA, Parkin K, Moore KH. Rectus fascia pubovaginal sling for recurrent stress urinary incontinence after failed synthetic mid-urethral sling: Letter. Canadian Urological Association Journal = Journal De L'Association Des Urologues Du Canada. 6: 429-30. PMID 23282658 DOI: 10.5489/cuaj.12132  0.4
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  1
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  1
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  1
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  1
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  1
2012 Healy EF, Walsh CA, Cotter AM, Walsh SR. Suprapubic compared with transurethral bladder catheterization for gynecologic surgery: a systematic review and meta-analysis. Obstetrics and Gynecology. 120: 678-87. PMID 22914481 DOI: 10.1097/AOG.0b013e3182657f0d  0.4
2012 Willems E, Cabral-Teixeira J, Schade D, Cai W, Reeves P, Bushway PJ, Lanier M, Walsh C, Kirchhausen T, Izpisua Belmonte JC, Cashman J, Mercola M. Small molecule-mediated TGF-β type II receptor degradation promotes cardiomyogenesis in embryonic stem cells. Cell Stem Cell. 11: 242-52. PMID 22862949 DOI: 10.1016/J.Stem.2012.04.025  1
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  1
2012 Sauls K, De Vlaming A, Harris BS, Williams K, Wessels A, Levine RA, Slaugenhaupt SA, Goodwin RL, Pavone LM, Merot J, Schott JJ, Le Tourneau T, Dix T, Jesinkey S, Feng Y, ... Walsh C, et al. Developmental basis for filamin-A-associated myxomatous mitral valve disease Cardiovascular Research. 96: 109-119. PMID 22843703 DOI: 10.1093/Cvr/Cvs238  1
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  1
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  1
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  1
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  1
2012 Walsh CA, Moore KH. Botulinum toxin in "refractory" detrusor overactivity. Re: Makovey I, et al. botulinum toxin outcomes for idiopathic overactive bladder stratified by indication: lack of anticholinergic efficacy versus intolerability. Neurourol Urodyn 2011;30:1538-1540. Neurourology and Urodynamics. 31: 708. PMID 22488771 DOI: 10.1002/nau.21237  0.4
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  1
2012 Walsh CA, McAuliffe FM. Recurrent twin-twin transfusion syndrome after selective fetoscopic laser photocoagulation: a systematic review of the literature. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 40: 506-12. PMID 22378622 DOI: 10.1002/uog.11105  0.4
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  1
2012 Moore KH, Shahab RB, Walsh CA, Kuteesa WM, Sarma S, Cebola M, Allen W, Wang YA, Karantanis E. Randomized controlled trial of cough test versus no cough test in the tension-free vaginal tape procedure: effect upon voiding dysfunction and 12-month efficacy. International Urogynecology Journal. 23: 435-41. PMID 22080364 DOI: 10.1007/s00192-011-1594-x  0.4
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  1
2011 Lees JN, Walsh CA. The contribution of Australian and New Zealand obstetrics and obstetricians and gynaecologists to modern clinical practice. The Medical Journal of Australia. 195: 614. PMID 22107014  0.4
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  1
2011 Chen J, Weber M, Um SY, Walsh CA, Tang Y, McDonald TV. A dual mechanism for I(Ks) current reduction by the pathogenic mutation KCNQ1-S277L. Pacing and Clinical Electrophysiology : Pace. 34: 1652-64. PMID 21895724 DOI: 10.1111/j.1540-8159.2011.03190.x  0.36
2011 Walsh CA. Recurrent stress urinary incontinence after synthetic mid-urethral sling procedures. Current Opinion in Obstetrics & Gynecology. 23: 355-61. PMID 21836507 DOI: 10.1097/GCO.0b013e32834a9282  0.4
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  1
2011 Walsh CA, Siddins A, Parkin K, Mukerjee C, Moore KH. Prevalence of "low-count" bacteriuria in female urinary incontinence versus continent female controls: a cross-sectional study. International Urogynecology Journal. 22: 1267-72. PMID 21796470 DOI: 10.1007/s00192-011-1506-0  0.4
2011 Walsh CA. TVT-Secur mini-sling for stress urinary incontinence: a review of outcomes at 12 months. Bju International. 108: 652-7. PMID 21756280 DOI: 10.1111/j.1464-410X.2011.10333.x  0.4
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  1
2011 Indraratna PL, Walsh CA, Moore KH. Intra-operative cystoscopy in gynaecological surgery: a brief overview. The Australian & New Zealand Journal of Obstetrics & Gynaecology. 51: 272-5. PMID 21631451 DOI: 10.1111/j.1479-828X.2010.01277.x  0.4
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  1
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  1
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  1
2011 Baxi LV, Walsh CA. Closure: an unusual postpartum problem was identified at the 6-week office visit. American Journal of Obstetrics and Gynecology. 204: 453.e1-2. PMID 21444062 DOI: 10.1016/j.ajog.2011.01.064  0.4
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  1
2011 Gendy R, Walsh CA, Walsh SR, Karantanis E. Vaginal hysterectomy versus total laparoscopic hysterectomy for benign disease: a metaanalysis of randomized controlled trials. American Journal of Obstetrics and Gynecology. 204: 388.e1-8. PMID 21377140 DOI: 10.1016/j.ajog.2010.12.059  0.4
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  1
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  1
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  1
2011 Clay FS, Walsh CA, Walsh SR. Staples vs subcuticular sutures for skin closure at cesarean delivery: a metaanalysis of randomized controlled trials. American Journal of Obstetrics and Gynecology. 204: 378-83. PMID 21195384 DOI: 10.1016/j.ajog.2010.11.018  0.4
2011 Walsh CA, Moore KH. Overactive bladder in women: does low-count bacteriuria matter? A review. Neurourology and Urodynamics. 30: 32-7. PMID 21046657 DOI: 10.1002/nau.20927  0.4
2011 Walsh CA, Allen W, Parkin K, Mukerjee C, Moore KH. Low-count bacteriuria in refractory idiopathic detrusor overactivity versus controls Urogynaecologia International Journal. 25: e4. DOI: 10.4081/uij.2011.e4  0.4
2011 Rabiner JE, Fagan MJ, Walsh CA. Can you read this electrocardiogram? Clinical Pediatric Emergency Medicine. 12: 333-342. DOI: 10.1016/j.cpem.2011.09.003  0.36
2011 Poduri A, Mellado C, Walsh CA. Response to "The Role of Cytomegalovirus in Schizencephaly" by Spalice et al American Journal of Medical Genetics, Part A. 155: 1769. DOI: 10.1002/ajmg.a.33925  1
2010 Walsh CA, Pistilli M, Karantanis E. Cardiac arrhythmias and gynaecological laparoscopy: a reminder. Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology. 30: 878-9. PMID 21126142 DOI: 10.3109/01443615.2010.518260  0.4
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  1
2010 Nicholson GT, Walsh CA, Madan RP. Transfusion-associated babesiosis in a 7-month-old infant after bidirectional Glenn procedure. Congenital Heart Disease. 5: 607-13. PMID 21106022 DOI: 10.1111/j.1747-0803.2010.00384.x  0.36
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  1
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  1
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  1
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  1
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  1
2010 Walsh CA, Ahmed S. RE: Pregnant until proven otherwise. Irish Medical Journal. 103: 221. PMID 20845607  0.4
2010 Yousef AF, Fonseca GJ, Pelka P, Ablack JN, Walsh C, Dick FA, Bazett-Jones DP, Shaw GS, Mymryk JS. Identification of a molecular recognition feature in the E1A oncoprotein that binds the SUMO conjugase UBC9 and likely interferes with polySUMOylation. Oncogene. 29: 4693-704. PMID 20543865 DOI: 10.1038/onc.2010.226  1
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  1
2010 Walsh CA, Moore KH. Recurrent stress urinary incontinence after synthetic midurethral sling procedure. Obstetrics and Gynecology. 115: 1296-301. PMID 20502302 DOI: 10.1097/AOG.0b013e3181da3a48  0.4
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  1
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  1
2010 Walsh CA, Allen W, Moore KH. 'Urinary incontinence' post-radiotherapy: a diagnostic conundrum. Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology. 30: 424-5. PMID 20455740 DOI: 10.3109/01443611003725464  0.4
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  1
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  1
2010 Son M, Walsh CA, Baxi LV. Prenatal diagnosis of urinary ascites in a fetus with meningomyelocele. Fetal Diagnosis and Therapy. 28: 61-4. PMID 20389051 DOI: 10.1159/000312405  0.4
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  1
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  1
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  1
2010 Walsh CA. Evidence-based cesarean technique. Current Opinion in Obstetrics & Gynecology. 22: 110-5. PMID 20216417 DOI: 10.1097/GCO.0b013e3283372327  0.4
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  1
2010 Cheng Y, Mansfield KJ, Allen W, Walsh CA, Burcher E, Moore KH. Does adenosine triphosphate released into voided urodynamic fluid contribute to urgency signaling in women with bladder dysfunction? The Journal of Urology. 183: 1082-6. PMID 20092837 DOI: 10.1016/j.juro.2009.11.028  0.4
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  1
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  1
2010 Baxi LV, Walsh CA. Monoamniotic twins in contemporary practice: a single-center study of perinatal outcomes. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 23: 506-10. PMID 19718582 DOI: 10.3109/14767050903214590  0.4
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  1
2010 Chang BS, Walsh CA. Heritable Microgyrias Encyclopedia of Neuroscience. 1107-1112. DOI: 10.1016/B978-008045046-9.01506-0  1
2010 Ferland RJ, Walsh CA. Joubert Syndrome Encyclopedia of Neuroscience. 249-256. DOI: 10.1016/B978-008045046-9.01487-X  1
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  1
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  1
2009 Bhutta HY, Walsh SR, Tang TY, Walsh CA, Clarke JM. Ovarian vein syndrome: a review. International Journal of Surgery (London, England). 7: 516-20. PMID 19818884 DOI: 10.1016/j.ijsu.2009.09.008  0.4
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  1
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  0.56
2009 Walsh CA, Walsh SR. Extraabdominal vs intraabdominal uterine repair at cesarean delivery: a metaanalysis. American Journal of Obstetrics and Gynecology. 200: 625.e1-8. PMID 19344883 DOI: 10.1016/j.ajog.2009.01.009  0.4
2009 Walsh CA, Walsh SR, Tang TY, Slack M. Total abdominal hysterectomy versus total laparoscopic hysterectomy for benign disease: a meta-analysis. European Journal of Obstetrics, Gynecology, and Reproductive Biology. 144: 3-7. PMID 19324491 DOI: 10.1016/j.ejogrb.2009.01.003  0.4
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  1
2009 Walsh CA, Walsh SR. Laparoscopic appendectomy during pregnancy: an evidence-based review. Surgical Endoscopy. 23: 671. PMID 19057951 DOI: 10.1007/s00464-008-0208-2  0.4
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2008 Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, Curry CJ, McDonald-McGinn D, Medne L, Zackai E, Parsons J, Zand DJ, Hisama FM, Walsh CA, Leventer RJ, et al. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2. American Journal of Medical Genetics. Part A. 146: 1637-54. PMID 18536050 DOI: 10.1002/ajmg.a.32293  1
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  1
2008 Walsh CA, Foley ME. Ehlers-danlos syndrome in pregnancy. Fetal Diagnosis and Therapy. 24: 79. PMID 18504388 DOI: 10.1159/000132413  0.4
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  1
2008 Walsh CA, Tang T, Walsh SR. Laparoscopic versus open appendicectomy in pregnancy: a systematic review. International Journal of Surgery (London, England). 6: 339-44. PMID 18342590 DOI: 10.1016/j.ijsu.2008.01.006  0.4
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  1
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  0.4
2008 Walsh CA, McMenamin MB, Foley ME, Daly SF, Robson MS, Geary MP. Trends in intrapartum fetal death, 1979-2003. American Journal of Obstetrics and Gynecology. 198: 47.e1-7. PMID 17905174 DOI: 10.1016/j.ajog.2007.06.018  0.4
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  1
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  1
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  1
2007 Shen Y, Irons M, Miller DT, Cheung SW, Lip V, Sheng X, Tomaszewicz K, Shao H, Fang H, Tang HS, Irons M, Walsh CA, Platt O, Gusella JF, Wu BL. Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance. Clinical Chemistry. 53: 2051-9. PMID 17901113 DOI: 10.1373/clinchem.2007.090290  1
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  1
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  1
2007 Walsh CA, Mahony RT, Foley ME, Daly L, O'Herlihy C. Recurrence of fetal macrosomia in non-diabetic pregnancies. Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology. 27: 374-8. PMID 17654189 DOI: 10.1080/01443610701327545  0.4
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  1
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  1
2007 Kim S, Walsh CA. Numb, neurogenesis and epithelial polarity. Nature Neuroscience. 10: 812-3. PMID 17593942 DOI: 10.1038/nn0707-812  0.4
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  1
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  0.56
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  1
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  1
2007 Walsh CA, Reardon W, Foley ME. Unexplained prelabor uterine rupture in a term primigravida. Obstetrics and Gynecology. 109: 455. PMID 17267858 DOI: 10.1097/01.AOG.0000244699.66548.e3  0.4
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  1
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  0.4
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  0.72
2006 Walsh CA, O'Sullivan RJ, Foley ME. Unexplained prelabor uterine rupture in a term primigravida. Obstetrics and Gynecology. 108: 725-7. PMID 17018479 DOI: 10.1097/01.AOG.0000195065.38149.11  0.4
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  1
2006 Sun T, Walsh CA. Molecular approaches to brain asymmetry and handedness. Nature Reviews. Neuroscience. 7: 655-62. PMID 16858393 DOI: 10.1038/nrn1930  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.4
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  1
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  0.56
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  1
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  1
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  1
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  1
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  1
2005 Hill RS, Walsh CA. Molecular insights into human brain evolution. Nature. 437: 64-7. PMID 16136130 DOI: 10.1038/nature04103  0.4
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  1
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  0.4
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  0.72
2005 Walsh CA, Quinlan DM. Oncocytoma and synchronous urothelial carcinoma in same kidney: previously unreported association. Urology. 66: 194. PMID 15921729 DOI: 10.1016/j.urology.2005.01.003  0.4
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.72
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  0.72
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  1
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  1
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  0.56
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  0.56
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  1
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  1
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  0.4
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  1
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  1
2004 Dickson B, Walsh CA. Development. Current Opinion in Neurobiology. 14: 1-5. PMID 15018931 DOI: 10.1016/j.conb.2004.01.016  1
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  1
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  1
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  0.36
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  1
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  1
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  1
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  1
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  1
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  1
2003 Kim MH, Cierpicki T, Derewenda U, Krowarsch D, Feng Y, Devedjiev Y, Dauter Z, Walsh CA, Otlewski J, Bushweller JH, Derewenda ZS. The DCX-domain tandems of doublecortin and doublecortin-like kinase. Nature Structural Biology. 10: 324-33. PMID 12692530 DOI: 10.1038/nsb918  1
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  1
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  1
2003 Sheen VL, Wheless JW, Bodell A, Braverman E, Cotter PD, Rauen KA, Glenn O, Weisiger K, Packman S, Walsh CA, Sherr EH. Periventricular heterotopia associated with chromosome 5p anomalies. Neurology. 60: 1033-6. PMID 12654978 DOI: 10.1212/01.Wnl.0000052689.03214.61  1
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  1
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  1
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  0.4
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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 : the Official Journal of the Society For Neuroscience. 21: 6772-81. PMID 11517265  1
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  0.72
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  0.4
2001 Barkovich AJ, Simon EM, Walsh CA. Callosal agenesis with cyst: a better understanding and new classification. Neurology. 56: 220-7. PMID 11160959 DOI: 10.1212/WNL.56.2.220  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2000 Vanderhaeghen P, Lu Q, Prakash N, Frisén J, Walsh CA, Frostig RD, Flanagan JG. A mapping label required for normal scale of body representation in the cortex. Nature Neuroscience. 3: 358-65. PMID 10725925 DOI: 10.1038/73929  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
1998 Berg MJ, Schifitto G, Powers JM, Martinez-Capolino C, Fong CT, Myers GJ, Epstein LG, Walsh CA. X-linked female band heterotopia-male lissencephaly syndrome. Neurology. 50: 1143-6. PMID 9566411  1
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  1
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  1
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  1
1996 Allen KM, Walsh C. Shaking down new epilepsy genes Nature Medicine. 2: 516-518. PMID 8616704 DOI: 10.1038/nm0596-516  1
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