| Year |
Citation |
Score |
| 2023 |
Wang B, Vartak R, Zaltsman Y, Naing ZZC, Hennick KM, Polacco BJ, Bashir A, Eckhardt M, Bouhaddou M, Xu J, Sun N, Lasser M, Zhou Y, Guiley KZ, Chan U, ... ... State MW, et al. A foundational atlas of autism protein interactions reveals molecular convergence. Biorxiv : the Preprint Server For Biology. PMID 38076945 DOI: 10.1101/2023.12.03.569805 |
0.838 |
|
| 2023 |
Wang S, Wang B, Drury V, Drake S, Sun N, Alkhairo H, Arbelaez J, Duhn C, Bal VH, Langley K, Martin J, Hoekstra PJ, Dietrich A, Xing J, Heiman GA, ... ... State MW, et al. Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD. Nature Communications. 14: 8077. PMID 38057346 DOI: 10.1038/s41467-023-43776-0 |
0.723 |
|
| 2023 |
Lasser M, Sun N, Xu Y, Wang S, Drake S, Law K, Gonzalez S, Wang B, Drury V, Castillo O, Zaltsman Y, Dea J, Bader E, McCluskey KE, State MW, et al. Pleiotropy of autism-associated chromatin regulators. Development (Cambridge, England). PMID 37366052 DOI: 10.1242/dev.201515 |
0.816 |
|
| 2022 |
Parellada M, Andreu-Bernabeu Á, Burdeus M, San José Cáceres A, Urbiola E, Carpenter LL, Kraguljac NV, McDonald WM, Nemeroff CB, Rodriguez CI, Widge AS, State MW, Sanders SJ. In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review. The American Journal of Psychiatry. appiajp21100992. PMID 36475375 DOI: 10.1176/appi.ajp.21100992 |
0.717 |
|
| 2022 |
Willsey HR, Willsey AJ, Wang B, State MW. Genomics, convergent neuroscience and progress in understanding autism spectrum disorder. Nature Reviews. Neuroscience. PMID 35440779 DOI: 10.1038/s41583-022-00576-7 |
0.821 |
|
| 2021 |
Markenscoff-Papadimitriou E, Binyameen F, Whalen S, Price J, Lim K, Ypsilanti AR, Catta-Preta R, Pai EL, Mu X, Xu D, Pollard KS, Nord AS, State MW, Rubenstein JL. Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes. Cell Reports. 37: 110089. PMID 34879283 DOI: 10.1016/j.celrep.2021.110089 |
0.835 |
|
| 2021 |
Willsey HR, Exner CRT, Xu Y, Everitt A, Sun N, Wang B, Dea J, Schmunk G, Zaltsman Y, Teerikorpi N, Kim A, Anderson AS, Shin D, Seyler M, Nowakowski TJ, ... ... State MW, et al. Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience. Neuron. 109: 1409. PMID 33887193 DOI: 10.1016/j.neuron.2021.03.030 |
0.776 |
|
| 2021 |
Willsey HR, Exner CRT, Xu Y, Everitt A, Sun N, Wang B, Dea J, Schmunk G, Zaltsman Y, Teerikorpi N, Kim A, Anderson AS, Shin D, Seyler M, Nowakowski TJ, ... ... State MW, et al. Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience. Neuron. PMID 33497602 DOI: 10.1016/j.neuron.2021.01.002 |
0.826 |
|
| 2021 |
Manoli DS, State MW. Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms. The American Journal of Psychiatry. 178: 30-38. PMID 33384012 DOI: 10.1176/appi.ajp.2020.20111608 |
0.552 |
|
| 2020 |
Willsey HR, Xu Y, Everitt A, Dea J, Exner CRT, Willsey AJ, State MW, Harland RM. Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in embryos. Development (Cambridge, England). 147. PMID 33288503 DOI: 10.1242/dev.198317 |
0.786 |
|
| 2020 |
Quick VBS, Wang B, State MW. Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 32668441 DOI: 10.1038/S41386-020-0768-Y |
0.646 |
|
| 2020 |
Markenscoff-Papadimitriou E, Whalen S, Przytycki P, Thomas R, Binyameen F, Nowakowski TJ, Kriegstein AR, Sanders SJ, State MW, Pollard KS, Rubenstein JL. A Chromatin Accessibility Atlas of the Developing Human Telencephalon. Cell. PMID 32610082 DOI: 10.1016/J.Cell.2020.06.002 |
0.811 |
|
| 2020 |
Willsey HR, Xu Y, Everitt A, Dea J, Exner CRT, Willsey AJ, State MW, Harland RM. Neurodevelopmental disorder risk gene is required for ciliogenesis and brain size in embryos. Development (Cambridge, England). PMID 32467234 DOI: 10.1242/Dev.189290 |
0.826 |
|
| 2020 |
Fazel Darbandi S, Robinson Schwartz SE, Pai EL, Everitt A, Turner ML, Cheyette BNR, Willsey AJ, State MW, Sohal VS, Rubenstein JLR. Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants. Cell Reports. 31: 107495. PMID 32294447 DOI: 10.1016/J.Celrep.2020.03.059 |
0.355 |
|
| 2020 |
Werling DM, Pochareddy S, Choi J, An JY, Sheppard B, Peng M, Li Z, Dastmalchi C, Santpere G, Sousa AMM, Tebbenkamp ATN, Kaur N, Gulden FO, Breen MS, Liang L, ... ... State MW, et al. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Reports. 31: 107489. PMID 32268104 DOI: 10.1016/J.Celrep.2020.03.053 |
0.828 |
|
| 2020 |
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, Peng M, Collins R, Grove J, Klei L, Stevens C, Reichert J, Mulhern MS, Artomov M, Gerges S, ... ... State MW, et al. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell. PMID 31981491 DOI: 10.1016/J.Cell.2019.12.036 |
0.855 |
|
| 2020 |
Lord C, Brugha TS, Charman T, Cusack J, Dumas G, Frazier T, Jones EJH, Jones RM, Pickles A, State MW, Taylor JL, Veenstra-VanderWeele J. Autism spectrum disorder. Nature Reviews. Disease Primers. 6: 5. PMID 31949163 DOI: 10.1038/s41572-019-0138-4 |
0.417 |
|
| 2019 |
State M. 11.1 THE REVOLUTION HAS BEGUN: ASD, GENOMICS, AND THE ADVANCING SCIENCE OF NEURODEVELOPMENTAL DISORDERS Journal of the American Academy of Child & Adolescent Psychiatry. 58: S315. DOI: 10.1016/J.Jaac.2019.07.728 |
0.456 |
|
| 2019 |
Werling D, Pochareddy S, Choi J, An J, Sheppard B, Peng M, Santpere G, Gulden F, Breen M, Talkowski M, Roeder K, State M, Devlin B, Sanders S, Sestan N. 29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX European Neuropsychopharmacology. 29: S75-S76. DOI: 10.1016/J.Euroneuro.2019.07.170 |
0.785 |
|
| 2019 |
An J, Lin K, Zhu L, Werling D, Dong S, Brand H, Wang H, Zhao X, Sestan N, State M, Willsey J, Talkowski M, Devlin B, Roeder K, Sanders S. INSIGHTS INTO THE CONTRIBUTION OF RARE NONCODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING European Neuropsychopharmacology. 29: S36. DOI: 10.1016/J.Euroneuro.2019.07.073 |
0.834 |
|
| 2019 |
Werling D, Brand H, An J, Stone M, Glessner J, Zhu L, Collins R, Daly M, State M, Quinlan A, Marth G, Roeder K, Devlin B, Sanders S, Talkowski M. LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES European Neuropsychopharmacology. 29: S784-S785. DOI: 10.1016/J.Euroneuro.2017.08.010 |
0.854 |
|
| 2019 |
Willsey J, Fernandez T, Yu D, King R, Dietrich A, Xing J, Sanders S, Mandell J, Neale B, Coppola G, Mathews C, Tischfield J, Scharf J, State M, Heiman G. De Novo Coding Variants Are Strongly Associated with Tourette Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.065 |
0.841 |
|
| 2018 |
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... State MW, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544. PMID 30566877 DOI: 10.1016/j.celrep.2018.12.024 |
0.819 |
|
| 2018 |
Li M, Santpere G, Imamura Kawasawa Y, Evgrafov OV, Gulden FO, Pochareddy S, Sunkin SM, Li Z, Shin Y, Zhu Y, Sousa AMM, Werling DM, Kitchen RR, Kang HJ, Pletikos M, ... ... State MW, et al. Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science (New York, N.Y.). 362. PMID 30545854 DOI: 10.1126/Science.Aat7615 |
0.827 |
|
| 2018 |
An JY, Lin K, Zhu L, Werling DM, Dong S, Brand H, Wang HZ, Zhao X, Schwartz GB, Collins RL, Currall BB, Dastmalchi C, Dea J, Duhn C, Gilson MC, ... ... State MW, et al. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362. PMID 30545852 DOI: 10.1126/Science.Aat6576 |
0.832 |
|
| 2018 |
Sestan N, State MW. Lost in Translation: Traversing the Complex Path from Genomics to Therapeutics in Autism Spectrum Disorder. Neuron. 100: 406-423. PMID 30359605 DOI: 10.1016/J.Neuron.2018.10.015 |
0.757 |
|
| 2018 |
Fazel Darbandi S, Robinson Schwartz SE, Qi Q, Catta-Preta R, Pai EL, Mandell JD, Everitt A, Rubin A, Krasnoff RA, Katzman S, Tastad D, Nord AS, Willsey AJ, Chen B, State MW, et al. Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity. Neuron. PMID 30318412 DOI: 10.1016/J.Neuron.2018.09.027 |
0.825 |
|
| 2018 |
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... State MW, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 24: 3441-3454.e12. PMID 30257206 DOI: 10.1016/J.Celrep.2018.08.082 |
0.855 |
|
| 2018 |
Willsey AJ, Morris MT, Wang S, Willsey HR, Sun N, Teerikorpi N, Baum TB, Cagney G, Bender KJ, Desai TA, Srivastava D, Davis GW, Doudna J, Chang E, Sohal V, ... ... State MW, et al. The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders. Cell. 174: 505-520. PMID 30053424 DOI: 10.1016/J.Cell.2018.06.016 |
0.826 |
|
| 2018 |
Werling DM, Brand H, An JY, Stone MR, Zhu L, Glessner JT, Collins RL, Dong S, Layer RM, Markenscoff-Papadimitriou E, Farrell A, Schwartz GB, Wang HZ, Currall BB, Zhao X, ... ... State MW, et al. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics. PMID 29700473 DOI: 10.1038/S41588-018-0107-Y |
0.83 |
|
| 2018 |
Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, ... ... State MW, et al. Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. PMID 29549319 DOI: 10.1038/S41593-018-0102-8 |
0.786 |
|
| 2018 |
Fernandez TV, State MW, Pittenger C. Tourette disorder and other tic disorders. Handbook of Clinical Neurology. 147: 343-354. PMID 29325623 DOI: 10.1016/B978-0-444-63233-3.00023-3 |
0.78 |
|
| 2018 |
Gothelf D, State M. 22Q11 Deletion Syndrome as a Genetic High-Risk Model for Developmental Neuropsychiatric Disorders: From Circuitry to Treatments Journal of the American Academy of Child & Adolescent Psychiatry. 57: S283. DOI: 10.1016/J.Jaac.2018.07.668 |
0.432 |
|
| 2018 |
Hoffman EJ, Manoli D, State M. From Bench to Bedside: Molecular and Genetic Mechanisms in Neurodevelopmental Disorders Journal of the American Academy of Child & Adolescent Psychiatry. 57: S275-S276. DOI: 10.1016/J.Jaac.2018.07.640 |
0.678 |
|
| 2017 |
Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, ... ... State MW, et al. Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. 20: 1661-1668. PMID 29184211 DOI: 10.1038/S41593-017-0017-9 |
0.832 |
|
| 2017 |
Sousa AMM, Zhu Y, Raghanti MA, Kitchen RR, Onorati M, Tebbenkamp ATN, Stutz B, Meyer KA, Li M, Kawasawa YI, Liu F, Perez RG, Mele M, Carvalho T, Skarica M, ... ... State MW, et al. Molecular and cellular reorganization of neural circuits in the human lineage. Science (New York, N.Y.). 358: 1027-1032. PMID 29170230 DOI: 10.1126/Science.Aan3456 |
0.75 |
|
| 2017 |
Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HAF, Pujol A, Distel B, Robak LA, Bernstein JA, ... ... State MW, et al. De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. American Journal of Human Genetics. 101: 768-788. PMID 29100089 DOI: 10.1016/J.Ajhg.2017.10.003 |
0.814 |
|
| 2017 |
Willsey AJ, Fernandez TV, Yu D, King RA, Dietrich A, Xing J, Sanders SJ, Mandell JD, Huang AY, Richer P, Smith L, Dong S, Samocha KE, ... ... State MW, et al. De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron. 94: 486-499.e9. PMID 28472652 DOI: 10.1016/J.Neuron.2017.04.024 |
0.85 |
|
| 2017 |
State M. 18.5 Progress in the Genetics of Autism Spectrum Disorder: From Genes to Emerging Neurobiology Journal of the American Academy of Child & Adolescent Psychiatry. 56: S330. DOI: 10.1016/J.Jaac.2017.07.684 |
0.507 |
|
| 2017 |
Hoffman EJ, State M. 18.0 Molecular and Genetic Mechanisms in Autism: From Bench to Bedside Journal of the American Academy of Child & Adolescent Psychiatry. 56: S329. DOI: 10.1016/J.Jaac.2017.07.679 |
0.639 |
|
| 2016 |
Georgitsi M, Willsey AJ, Mathews CA, State M, Scharf JM, Paschou P. The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery. Frontiers in Neuroscience. 10: 351. PMID 27536211 DOI: 10.3389/Fnins.2016.00351 |
0.805 |
|
| 2016 |
Abdulkadir M, Tischfield JA, King RA, Fernandez TV, Brown LW, Cheon KA, Coffey BJ, de Bruijn SF, Elzerman L, Garcia-Delgar B, Gilbert DL, Grice DE, Hagstrøm J, Hedderly T, Heyman I, ... ... State MW, et al. Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder. Journal of Psychiatric Research. 82: 126-135. PMID 27494079 DOI: 10.1016/J.Jpsychires.2016.07.017 |
0.706 |
|
| 2016 |
Anazi S, Maddirevula S, Faqeih E, Alsedairy H, Alzahrani F, Shamseldin HE, Patel N, Hashem M, Ibrahim N, Abdulwahab F, Ewida N, Alsaif HS, Al Sharif H, Alamoudi W, Kentab A, ... ... State M, et al. Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield. Molecular Psychiatry. PMID 27431290 DOI: 10.1038/Mp.2016.113 |
0.56 |
|
| 2016 |
Fraguas D, Díaz-Caneja CM, State MW, O'Donovan MC, Gur RE, Arango C. Mental disorders of known aetiology and precision medicine in psychiatry: a promising but neglected alliance. Psychological Medicine. 1-5. PMID 27334937 DOI: 10.1017/S0033291716001355 |
0.384 |
|
| 2016 |
Hoffman EJ, Turner KJ, Fernandez JM, Cifuentes D, Ghosh M, Ijaz S, Jain RA, Kubo F, Bill BR, Baier H, Granato M, Barresi MJ, Wilson SW, Rihel J, State MW, et al. Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2. Neuron. PMID 26833134 DOI: 10.1016/J.Neuron.2015.12.039 |
0.697 |
|
| 2016 |
Ijaz S, Ghosh M, Wilson S, Rihel J, Giraldez AJ, State M, Hoffman EJ. 5.32 A ZEBRAFISH MODEL FOR IDENTIFYING COMMON BIOLOGICAL MECHANISMS AND PHARMACOLOGICAL PATHWAYS IN AUTISM SPECTRUM DISORDERS Journal of the American Academy of Child & Adolescent Psychiatry. 55: S194. DOI: 10.1016/J.Jaac.2016.09.291 |
0.688 |
|
| 2016 |
State M. 23.1 MOVING FROM GENES TO NEUROBIOLOGY IN NEURODEVELOPMENTAL DISORDERS Journal of the American Academy of Child & Adolescent Psychiatry. 55: S293. DOI: 10.1016/J.Jaac.2016.07.250 |
0.463 |
|
| 2016 |
Hoffman EJ, State M. 20.0 Molecular and Genetic Mechanisms in Autism Spectrum Disorder: From Bench to Bedside Journal of the American Academy of Child & Adolescent Psychiatry. 55: S288. DOI: 10.1016/J.Jaac.2016.07.231 |
0.692 |
|
| 2015 |
Lin Z, Sanders SJ, Li M, Sestan N, State MW, Zhao H. A MARKOV RANDOM FIELD-BASED APPROACH TO CHARACTERIZING HUMAN BRAIN DEVELOPMENT USING SPATIAL-TEMPORAL TRANSCRIPTOME DATA. The Annals of Applied Statistics. 9: 429-451. PMID 26877824 DOI: 10.1214/14-Aoas802 |
0.782 |
|
| 2015 |
Akbarian S, Liu C, Knowles JA, Vaccarino FM, Farnham PJ, Crawford GE, Jaffe AE, Pinto D, Dracheva S, Geschwind DH, Mill J, Nairn AC, Abyzov A, Pochareddy S, Prabhakar S, ... ... State MW, et al. The PsychENCODE project. Nature Neuroscience. 18: 1707-1712. PMID 26605881 DOI: 10.1038/Nn.4156 |
0.836 |
|
| 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, ... ... State MW, 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 |
0.839 |
|
| 2015 |
Geschwind DH, State MW. Gene hunting in autism spectrum disorder: on the path to precision medicine. The Lancet. Neurology. PMID 25891009 DOI: 10.1016/S1474-4422(15)00044-7 |
0.67 |
|
| 2015 |
Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D, Pihur V, Plona T, Pike K, Soppet DR, Smith MW, ... ... State MW, et al. Loss of δ-catenin function in severe autism. Nature. 520: 51-6. PMID 25807484 DOI: 10.1038/Nature14186 |
0.791 |
|
| 2015 |
Cotney J, Muhle RA, Sanders SJ, Liu L, Willsey AJ, Niu W, Liu W, Klei L, Lei J, Yin J, Reilly SK, Tebbenkamp AT, Bichsel C, Pletikos M, Sestan N, ... ... State MW, et al. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment. Nature Communications. 6: 6404. PMID 25752243 DOI: 10.1038/Ncomms7404 |
0.832 |
|
| 2015 |
Murdoch JD, Gupta AR, Sanders SJ, Walker MF, Keaney J, Fernandez TV, Murtha MT, Anyanwu S, Ober GT, Raubeson MJ, DiLullo NM, Villa N, Waqar Z, Sullivan C, Gonzalez L, ... ... State MW, et al. No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins. Plos Genetics. 11: e1004852. PMID 25621974 DOI: 10.1371/Journal.Pgen.1004852 |
0.832 |
|
| 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, ... ... State MW, 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 |
0.833 |
|
| 2015 |
State MW, Geschwind DH. Leveraging genetics and genomics to define the causes of mental illness. Biological Psychiatry. 77: 3-5. PMID 25483342 DOI: 10.1016/J.Biopsych.2014.11.003 |
0.567 |
|
| 2015 |
Willsey AJ, State MW. Autism spectrum disorders: from genes to neurobiology. Current Opinion in Neurobiology. 30: 92-9. PMID 25464374 DOI: 10.1016/J.Conb.2014.10.015 |
0.816 |
|
| 2015 |
Ercan-Sencicek AG, Jambi S, Franjic D, Nishimura S, Li M, El-Fishawy P, Morgan TM, Sanders SJ, Bilguvar K, Suri M, Johnson MH, Gupta AR, Yuksel Z, Mane S, Grigorenko E, ... ... State MW, et al. Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. European Journal of Human Genetics : Ejhg. 23: 165-72. PMID 24781755 DOI: 10.1038/Ejhg.2014.82 |
0.818 |
|
| 2015 |
Dietrich A, Fernandez TV, King RA, State MW, Tischfield JA, Hoekstra PJ, Heiman GA. The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods. European Child & Adolescent Psychiatry. 24: 141-51. PMID 24771252 DOI: 10.1007/S00787-014-0543-X |
0.756 |
|
| 2015 |
Lin Z, Sanders SJ, Li M, Sestan N, State MW, Zhao H. A markov random field-based approach to characterizing human brain development using spatial–temporal transcriptome data Annals of Applied Statistics. 9: 429-451. DOI: 10.1214/14-AOAS802 |
0.754 |
|
| 2014 |
Pauls DL, Fernandez TV, Mathews CA, State MW, Scharf JM. The Inheritance of Tourette Disorder: A review. Journal of Obsessive-Compulsive and Related Disorders. 3: 380-385. PMID 25506544 DOI: 10.1016/J.Jocrd.2014.06.003 |
0.754 |
|
| 2014 |
Griesi-Oliveira K, Acab A, Gupta AR, Sunaga DY, Chailangkarn T, Nicol X, Nunez Y, Walker MF, Murdoch JD, Sanders SJ, Fernandez TV, Ji W, Lifton RP, Vadasz E, Dietrich A, ... ... State MW, et al. Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons. Molecular Psychiatry. PMID 25385366 DOI: 10.1038/Mp.2014.141 |
0.83 |
|
| 2014 |
Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, ... ... State MW, et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature. 515: 216-21. PMID 25363768 DOI: 10.1038/Nature13908 |
0.825 |
|
| 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, ... ... State MW, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.834 |
|
| 2014 |
Dong S, Walker MF, Carriero NJ, DiCola M, Willsey AJ, Ye AY, Waqar Z, Gonzalez LE, Overton JD, Frahm S, Keaney JF, Teran NA, Dea J, Mandell JD, Hus Bal V, ... ... State MW, et al. De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. Cell Reports. 9: 16-23. PMID 25284784 DOI: 10.1016/J.Celrep.2014.08.068 |
0.853 |
|
| 2014 |
Glessner JT, Bick AG, Ito K, Homsy JG, Rodriguez-Murillo L, Fromer M, Mazaika E, Vardarajan B, Italia M, Leipzig J, DePalma SR, Golhar R, Sanders SJ, Yamrom B, Ronemus M, ... ... State MW, et al. Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data. Circulation Research. 115: 884-96. PMID 25205790 DOI: 10.1161/Circresaha.115.304458 |
0.788 |
|
| 2014 |
Gupta AR, Pirruccello M, Cheng F, Kang HJ, Fernandez TV, Baskin JM, Choi M, Liu L, Ercan-Sencicek AG, Murdoch JD, Klei L, Neale BM, Franjic D, Daly MJ, Lifton RP, ... ... State MW, et al. Rare deleterious mutations of the gene EFR3A in autism spectrum disorders. Molecular Autism. 5: 31. PMID 24860643 DOI: 10.1186/2040-2392-5-31 |
0.844 |
|
| 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, ... ... State MW, 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 |
0.839 |
|
| 2014 |
Krystal JH, State MW. Psychiatric disorders: diagnosis to therapy. Cell. 157: 201-14. PMID 24679536 DOI: 10.1016/J.Cell.2014.02.042 |
0.374 |
|
| 2014 |
Kim YS, State MW. Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders. International Journal of Epidemiology. 43: 465-75. PMID 24618187 DOI: 10.1093/Ije/Dyu037 |
0.613 |
|
| 2014 |
Liu L, Lei J, Sanders SJ, Willsey AJ, Kou Y, Cicek AE, Klei L, Lu C, He X, Li M, Muhle RA, Ma'ayan A, Noonan JP, Sestan N, McFadden KA, ... State MW, et al. DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics. Molecular Autism. 5: 22. PMID 24602502 DOI: 10.1186/2040-2392-5-22 |
0.845 |
|
| 2014 |
Tebbenkamp AT, Willsey AJ, State MW, Sestan N. The developmental transcriptome of the human brain: implications for neurodevelopmental disorders. Current Opinion in Neurology. 27: 149-56. PMID 24565942 DOI: 10.1097/Wco.0000000000000069 |
0.831 |
|
| 2014 |
Volkmar F, Siegel M, Woodbury-Smith M, King B, McCracken J, State M. Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 237-57. PMID 24472258 DOI: 10.1016/J.Jaac.2013.10.013 |
0.507 |
|
| 2014 |
Castellan Baldan L, Williams KA, Gallezot JD, Pogorelov V, Rapanelli M, Crowley M, Anderson GM, Loring E, Gorczyca R, Billingslea E, Wasylink S, Panza KE, Ercan-Sencicek AG, Krusong K, Leventhal BL, ... ... State MW, et al. Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice. Neuron. 81: 77-90. PMID 24411733 DOI: 10.1016/J.Neuron.2013.10.052 |
0.323 |
|
| 2014 |
Ahn K, Gotay N, Andersen TM, Anvari AA, Gochman P, Lee Y, Sanders S, Guha S, Darvasi A, Glessner JT, Hakonarson H, Lencz T, State MW, Shugart YY, Rapoport JL. High rate of disease-related copy number variations in childhood onset schizophrenia. Molecular Psychiatry. 19: 568-72. PMID 23689535 DOI: 10.1038/Mp.2013.59 |
0.769 |
|
| 2013 |
Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, ... ... State MW, et al. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell. 155: 997-1007. PMID 24267886 DOI: 10.1016/J.Cell.2013.10.020 |
0.847 |
|
| 2013 |
He X, Sanders SJ, Liu L, De Rubeis S, Lim ET, Sutcliffe JS, Schellenberg GD, Gibbs RA, Daly MJ, Buxbaum JD, State MW, Devlin B, Roeder K. Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. Plos Genetics. 9: e1003671. PMID 23966865 DOI: 10.1371/Journal.Pgen.1003671 |
0.849 |
|
| 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, ... ... State M, 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 |
0.823 |
|
| 2013 |
Sanna-Cherchi S, Sampogna RV, Papeta N, Burgess KE, Nees SN, Perry BJ, Choi M, Bodria M, Liu Y, Weng PL, Lozanovski VJ, Verbitsky M, Lugani F, Sterken R, Paragas N, ... ... State M, et al. Mutations in DSTYK and dominant urinary tract malformations. The New England Journal of Medicine. 369: 621-9. PMID 23862974 DOI: 10.1056/NEJMoa1214479 |
0.71 |
|
| 2013 |
Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M, Triche EW, Geschwind DH, State MW, Istrail S, Cook EH, Devlin B, Morrow EM. Intellectual disability is associated with increased runs of homozygosity in simplex autism. American Journal of Human Genetics. 93: 103-9. PMID 23830515 DOI: 10.1016/J.Ajhg.2013.06.004 |
0.859 |
|
| 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, ... ... State MW, 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 |
0.813 |
|
| 2013 |
Zaidi S, Choi M, Wakimoto H, Ma L, Jiang J, Overton JD, Romano-Adesman A, Bjornson RD, Breitbart RE, Brown KK, Carriero NJ, Cheung YH, Deanfield J, DePalma S, Fakhro KA, ... ... State MW, et al. De novo mutations in histone-modifying genes in congenital heart disease. Nature. 498: 220-3. PMID 23665959 DOI: 10.1038/Nature12141 |
0.813 |
|
| 2013 |
Murdoch JD, State MW. Recent developments in the genetics of autism spectrum disorders. Current Opinion in Genetics & Development. 23: 310-5. PMID 23537858 DOI: 10.1016/J.Gde.2013.02.003 |
0.831 |
|
| 2013 |
Zuo L, Wang K, Zhang XY, Pan X, Wang G, Tan Y, Zhong C, Krystal JH, State M, Zhang H, Luo X. Association between common alcohol dehydrogenase gene (ADH) variants and schizophrenia and autism. Human Genetics. 132: 735-43. PMID 23468174 DOI: 10.1007/S00439-013-1277-4 |
0.44 |
|
| 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, ... ... State MW, 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 |
0.823 |
|
| 2013 |
Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, ... ... State MW, et al. Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron. 77: 235-42. PMID 23352160 DOI: 10.1016/J.Neuron.2012.12.029 |
0.843 |
|
| 2013 |
Clark VE, Erson-Omay EZ, Serin A, Yin J, Cotney J, Ozduman K, Avşar T, Li J, Murray PB, Henegariu O, Yilmaz S, Günel JM, Carrión-Grant G, Yilmaz B, Grady C, ... ... State MW, et al. Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO. Science (New York, N.Y.). 339: 1077-80. PMID 23348505 DOI: 10.1126/science.1233009 |
0.716 |
|
| 2013 |
Moreno-De-Luca D, Sanders SJ, Willsey AJ, Mulle JG, Lowe JK, Geschwind DH, State MW, Martin CL, Ledbetter DH. Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts. Molecular Psychiatry. 18: 1090-5. PMID 23044707 DOI: 10.1038/Mp.2012.138 |
0.84 |
|
| 2013 |
Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... State MW, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69 |
0.737 |
|
| 2012 |
Buxbaum JD, Daly MJ, Devlin B, Lehner T, Roeder K, State MW. The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders. Neuron. 76: 1052-6. PMID 23259942 DOI: 10.1016/J.Neuron.2012.12.008 |
0.718 |
|
| 2012 |
Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini A, Corbani V, ... ... State M, et al. Copy-number disorders are a common cause of congenital kidney malformations. American Journal of Human Genetics. 91: 987-97. PMID 23159250 DOI: 10.1016/J.Ajhg.2012.10.007 |
0.844 |
|
| 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, ... ... State MW, 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 |
0.831 |
|
| 2012 |
State MW, Šestan N. Neuroscience. The emerging biology of autism spectrum disorders. Science (New York, N.Y.). 337: 1301-3. PMID 22984058 DOI: 10.1126/Science.1224989 |
0.711 |
|
| 2012 |
Novarino G, El-Fishawy P, Kayserili H, Meguid NA, Scott EM, Schroth J, Silhavy JL, Kara M, Khalil RO, Ben-Omran T, Ercan-Sencicek AG, Hashish AF, Sanders SJ, Gupta AR, Hashem HS, ... ... State MW, et al. Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy. Science (New York, N.Y.). 338: 394-7. PMID 22956686 DOI: 10.1126/Science.1224631 |
0.812 |
|
| 2012 |
Luo R, Sanders SJ, Tian Y, Voineagu I, Huang N, Chu SH, Klei L, Cai C, Ou J, Lowe JK, Hurles ME, Devlin B, State MW, Geschwind DH. Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. American Journal of Human Genetics. 91: 38-55. PMID 22726847 DOI: 10.1016/J.Ajhg.2012.05.011 |
0.857 |
|
| 2012 |
Griesi-Oliveira K, Moreira Dde P, Davis-Wright N, Sanders S, Mason C, Orabona GM, Vadasz E, Bertola DR, State MW, Passos-Bueno MR. A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 529-36. PMID 22592906 DOI: 10.1002/Ajmg.B.32059 |
0.795 |
|
| 2012 |
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, ... ... State MW, et al. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 485: 237-41. PMID 22495306 DOI: 10.1038/Nature10945 |
0.84 |
|
| 2012 |
Gulhan Ercan-Sencicek A, Davis Wright NR, Frost SJ, Fulbright RK, Felsenfeld S, Hart L, Landi N, Einar Mencl W, Sanders SJ, Pugh KR, State MW, Grigorenko EL. Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism. Brain & Development. 34: 700-3. PMID 22178197 DOI: 10.1016/J.Braindev.2011.11.003 |
0.737 |
|
| 2012 |
Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO, Raubeson MJ, Song Y, Yasuno K, Ho WS, Bilguvar K, Glessner J, Chu SH, Leckman JF, King RA, ... ... State MW, et al. Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biological Psychiatry. 71: 392-402. PMID 22169095 DOI: 10.1016/J.Biopsych.2011.09.034 |
0.842 |
|
| 2012 |
Scharf J, Yu D, Mathews C, Neale B, Stewart E, Fagerness J, Evans P, Gamazon E, Service S, Osiecki L, Illmann C, Cath D, King R, Dion Y, Sandor P, ... ... State M, et al. Genome-Wide Association Study of Gilles de la Tourette Syndrome (IN10-1.002) Neurology. 78: IN10-1.002-IN10-1.00. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In10-1.002 |
0.392 |
|
| 2011 |
State MW, Levitt P. The conundrums of understanding genetic risks for autism spectrum disorders. Nature Neuroscience. 14: 1499-506. PMID 22037497 DOI: 10.1038/Nn.2924 |
0.578 |
|
| 2011 |
Celestino-Soper PB, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH, ... ... State MW, et al. Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Human Molecular Genetics. 20: 4360-70. PMID 21865298 DOI: 10.1093/Hmg/Ddr363 |
0.795 |
|
| 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, ... ... State MW, 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 |
0.827 |
|
| 2011 |
State MW. The erosion of phenotypic specificity in psychiatric genetics: emerging lessons from CNTNAP2. Biological Psychiatry. 69: 816-7. PMID 21497679 DOI: 10.1016/J.Biopsych.2011.03.021 |
0.398 |
|
| 2011 |
Bloch M, State M, Pittenger C. Recent advances in Tourette syndrome Current Opinion in Neurology. 24: 119-125. PMID 21386676 DOI: 10.1097/Wco.0B013E328344648C |
0.39 |
|
| 2011 |
State MW. The genetics of Tourette disorder. Current Opinion in Genetics & Development. 21: 302-9. PMID 21277193 DOI: 10.1016/J.Gde.2011.01.007 |
0.574 |
|
| 2010 |
State MW. The genetics of child psychiatric disorders: focus on autism and Tourette syndrome. Neuron. 68: 254-69. PMID 20955933 DOI: 10.1016/J.Neuron.2010.10.004 |
0.476 |
|
| 2010 |
Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizo?lu D, Tüysüz B, Ca?layan AO, Gökben S, Kaymakçalan H, Barak T, Bakircio?lu M, Yasuno K, Ho W, ... ... State MW, et al. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature. 467: 207-10. PMID 20729831 DOI: 10.1038/Nature09327 |
0.821 |
|
| 2010 |
Hoffman EJ, State MW. Progress in cytogenetics: implications for child psychopathology. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 736-51; quiz 856-7. PMID 20643309 DOI: 10.1016/J.Jaac.2010.03.016 |
0.698 |
|
| 2010 |
State MW. Another piece of the autism puzzle. Nature Genetics. 42: 478-9. PMID 20502490 DOI: 10.1038/Ng0610-478 |
0.366 |
|
| 2010 |
Bayrakli F, Bilguvar K, Ceyhan D, Ercan-Sencicek AG, Cankaya T, Bayrakli S, Guney I, Mane SM, State MW, Gunel M. Heterozygous 5p13.3-13.2 deletion in a patient with type I Chiari malformation and bilateral Duane retraction syndrome. Clinical Genetics. 77: 499-502. PMID 20447154 DOI: 10.1111/J.1399-0004.2010.01411.X |
0.58 |
|
| 2010 |
Ercan-Sencicek AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE, Abbott T, Gupta A, King RA, Pauls DL, Tischfield JA, Heiman GA, Singer HS, Gilbert DL, Hoekstra PJ, ... ... State MW, et al. L-histidine decarboxylase and Tourette's syndrome. The New England Journal of Medicine. 362: 1901-8. PMID 20445167 DOI: 10.1056/Nejmoa0907006 |
0.817 |
|
| 2010 |
Yasuno K, Bilguvar K, Bijlenga P, Low SK, Krischek B, Auburger G, Simon M, Krex D, Arlier Z, Nayak N, Ruigrok YM, Niemelä M, Tajima A, von und zu Fraunberg M, Dóczi T, ... ... State MW, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nature Genetics. 42: 420-5. PMID 20364137 DOI: 10.1038/Ng.563 |
0.668 |
|
| 2010 |
Erturk O, Bilguvar K, Korkmaz B, Bayri Y, Bayrakli F, Arlier Z, Ozturk AK, Yalcinkaya C, Tuysuz B, State MW, Gunel M. A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting Dystrophin. American Journal of Medical Genetics. Part A. 152: 1039-42. PMID 20358624 DOI: 10.1002/Ajmg.A.33312 |
0.511 |
|
| 2010 |
O'Roak BJ, Morgan TM, Fishman DO, Saus E, Alonso P, Gratacòs M, Estivill X, Teltsh O, Kohn Y, Kidd KK, Cho J, Lifton RP, State MW. Additional support for the association of SLITRK1 var321 and Tourette syndrome. Molecular Psychiatry. 15: 447-50. PMID 20351724 DOI: 10.1038/Mp.2009.105 |
0.8 |
|
| 2010 |
El-Fishawy P, State MW. The genetics of autism: key issues, recent findings, and clinical implications. The Psychiatric Clinics of North America. 33: 83-105. PMID 20159341 DOI: 10.1016/J.Psc.2009.12.002 |
0.512 |
|
| 2010 |
Kolb LE, Arlier Z, Yalcinkaya C, Ozturk AK, Moliterno JA, Erturk O, Bayrakli F, Korkmaz B, DiLuna ML, Yasuno K, Bilguvar K, Ozcelik T, Tuysuz B, State MW, Gunel M. Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy. Neurogenetics. 11: 319-25. PMID 20082205 DOI: 10.1007/S10048-009-0232-Y |
0.634 |
|
| 2010 |
Fernandez TV, State MW, Davalos-Rodriguez NO. Reply to 3p deletion and (skewed) literature review American Journal of Medical Genetics, Part A. 152: 1060. DOI: 10.1002/Ajmg.A.33150 |
0.584 |
|
| 2009 |
DiLuna ML, Bilguvar K, Louvi A, Bizzarro M, Bayrakli F, Bayri Y, Bydon M, Schneider K, Duncan CC, State M, Lifton RP, Ment LR, Gunel M. Mutations in the Type IV Collagens, COL4A1 and COL4A2 are Associated with Intraventricular Hemorrhage in Preterm Infants: 956. Neurosurgery. 65: 419. PMID 28173201 DOI: 10.1227/01.Neu.0000358727.92507.Ea |
0.682 |
|
| 2009 |
Bilguvar K, Ozturk AK, Bayrakli F, Guzel A, DiLuna ML, Bayri Y, Tatli M, Tekes S, Arlier Z, Yasuno K, Mason CE, Lifton RP, State MW, Gunel M. The syndrome of pachygyria, mental retardation, and arachnoid cysts maps to 11p15. American Journal of Medical Genetics. Part A. 149: 2569-72. PMID 19876906 DOI: 10.1002/Ajmg.A.33063 |
0.721 |
|
| 2009 |
Bayrakli F, Guney I, Bayri Y, Ercan-Sencicek AG, Ceyhan D, Cankaya T, Mason C, Bilguvar K, Bayrakli S, Mane SM, State MW, Gunel M. A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family group. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 16: 1610-4. PMID 19793656 DOI: 10.1016/J.Jocn.2009.03.022 |
0.72 |
|
| 2009 |
Johnson MB, Kawasawa YI, Mason CE, Krsnik Z, Coppola G, Bogdanovi? D, Geschwind DH, Mane SM, State MW, Sestan N. Functional and evolutionary insights into human brain development through global transcriptome analysis. Neuron. 62: 494-509. PMID 19477152 DOI: 10.1016/J.Neuron.2009.03.027 |
0.739 |
|
| 2009 |
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, ... ... State MW, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.629 |
|
| 2009 |
Volkmar FR, State M, Klin A. Autism and autism spectrum disorders: diagnostic issues for the coming decade. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 50: 108-15. PMID 19220594 DOI: 10.1111/J.1469-7610.2008.02010.X |
0.429 |
|
| 2009 |
Stillman AA, Krsnik Z, Sun J, Rasin MR, State MW, Sestan N, Louvi A. Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome. The Journal of Comparative Neurology. 513: 21-37. PMID 19105198 DOI: 10.1002/Cne.21919 |
0.8 |
|
| 2008 |
O'Roak BJ, State MW. Autism genetics: strategies, challenges, and opportunities. Autism Research : Official Journal of the International Society For Autism Research. 1: 4-17. PMID 19360646 DOI: 10.1002/Aur.3 |
0.776 |
|
| 2008 |
Bilguvar K, Yasuno K, Niemelä M, Ruigrok YM, von Und Zu Fraunberg M, van Duijn CM, van den Berg LH, Mane S, Mason CE, Choi M, Gaál E, Bayri Y, Kolb L, Arlier Z, Ravuri S, ... ... State MW, et al. Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nature Genetics. 40: 1472-7. PMID 18997786 DOI: 10.1038/Ng.240 |
0.729 |
|
| 2008 |
Fernandez TV, García-González IJ, Mason CE, Hernández-Zaragoza G, Ledezma-Rodríguez VC, Anguiano-Alvarez VM, E'Vega R, Gutiérrez-Angulo M, Maya ML, García-Bejarano HE, González-Cruz M, Barrios S, Atorga R, López-Cardona MG, Armendariz-Borunda J, ... State MW, et al. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature. American Journal of Medical Genetics. Part A. 146: 2746-52. PMID 18837054 DOI: 10.1002/Ajmg.A.32533 |
0.721 |
|
| 2008 |
Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW. Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. American Journal of Human Genetics. 82: 1385. PMID 18551756 DOI: 10.1016/j.ajhg.2008.04.021 |
0.711 |
|
| 2008 |
Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nature Genetics. 40: 592-9. PMID 18391953 DOI: 10.1038/Ng.118 |
0.815 |
|
| 2008 |
Tüysüz B, Bayrakli F, DiLuna ML, Bilguvar K, Bayri Y, Yalcinkaya C, Bursali A, Ozdamar E, Korkmaz B, Mason CE, Ozturk AK, Lifton RP, State MW, Gunel M. Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population. Neurogenetics. 9: 119-25. PMID 18322713 DOI: 10.1007/S10048-008-0121-9 |
0.774 |
|
| 2008 |
Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, ... ... State MW, et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. American Journal of Human Genetics. 82: 165-73. PMID 18179895 DOI: 10.1016/J.Ajhg.2007.09.017 |
0.845 |
|
| 2008 |
Speed WC, O'Roak BJ, Tárnok Z, Barta C, Pakstis AJ, State MW, Kidd KK. Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 463-6. PMID 18004766 DOI: 10.1002/Ajmg.B.30641 |
0.764 |
|
| 2007 |
Bilguvar K, Bydon M, Bayrakli F, Ercan-Sencicek AG, Bayri Y, Mason C, DiLuna ML, Seashore M, Bronen R, Lifton RP, State M, Gunel M. A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly: Laboratory investigation Journal of Neurosurgery. 107: 495-499. PMID 18154020 DOI: 10.3171/Ped-07/12/495 |
0.773 |
|
| 2007 |
Bayrakli F, Bilguvar K, Mason CE, DiLuna ML, Bayri Y, Gungor L, Terzi M, Mane SM, Lifton RP, State MW, Gunel M. Rapid identification of disease-causing mutations using copy number analysis within linkage intervals. Human Mutation. 28: 1236-40. PMID 17676595 DOI: 10.1002/Humu.20592 |
0.802 |
|
| 2007 |
Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... State M, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.728 |
|
| 2007 |
Gupta AR, State MW. Recent advances in the genetics of autism. Biological Psychiatry. 61: 429-37. PMID 16996486 DOI: 10.1016/J.Biopsych.2006.06.020 |
0.699 |
|
| 2006 |
State MW. A surprising METamorphosis: autism genetics finds a common functional variant. Proceedings of the National Academy of Sciences of the United States of America. 103: 16621-2. PMID 17075042 DOI: 10.1073/Pnas.0608027103 |
0.546 |
|
| 2006 |
Gupta AR, State MW. [Autism: genetics]. Revista Brasileira De Psiquiatria (SãO Paulo, Brazil : 1999). 28: S29-38. PMID 16791389 DOI: 10.1590/S1516-44462006000500005 |
0.675 |
|
| 2006 |
Plant LD, Bowers PN, Liu Q, Morgan T, Zhang T, State MW, Chen W, Kittles RA, Goldstein SA. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. The Journal of Clinical Investigation. 116: 430-5. PMID 16453024 DOI: 10.1172/Jci25618 |
0.347 |
|
| 2005 |
Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, ... ... State MW, et al. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science (New York, N.Y.). 310: 317-20. PMID 16224024 DOI: 10.1126/Science.1116502 |
0.819 |
|
| 2005 |
Drazinic CM, Ercan-Sencicek AG, Gault LM, Hisama FM, Qumsiyeh MB, Nowak NJ, Cubells JF, State MW. Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23). American Journal of Medical Genetics. Part A. 134: 282-9. PMID 15754353 DOI: 10.1002/Ajmg.A.30616 |
0.305 |
|
| 2005 |
Mani A, Radhakrishnan J, Farhi A, Carew KS, Warnes CA, Nelson-Williams C, Day RW, Pober B, State MW, Lifton RP. Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder. Proceedings of the National Academy of Sciences of the United States of America. 102: 2975-9. PMID 15684060 DOI: 10.1073/Pnas.0409852102 |
0.678 |
|
| 2005 |
Nahed BV, Seker A, Guclu B, Ozturk AK, Finberg K, Hawkins AA, DiLuna ML, State M, Lifton RP, Gunel M. Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13. American Journal of Human Genetics. 76: 172-9. PMID 15540160 DOI: 10.1086/426953 |
0.805 |
|
| 2004 |
Cuker A, State MW, King RA, Davis N, Ward DC. Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22. American Journal of Medical Genetics. Part A. 130: 37-9. PMID 15368493 DOI: 10.1002/Ajmg.A.30066 |
0.627 |
|
| 2004 |
Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW. Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. American Journal of Human Genetics. 74: 1286-93. PMID 15106122 DOI: 10.1086/421474 |
0.767 |
|
| 2004 |
Fernandez T, State M. Genetics and Genomics of Neurobehavioral Disorders Journal of the American Academy of Child & Adolescent Psychiatry. 43: 370-371. DOI: 10.1097/00004583-200403000-00021 |
0.713 |
|
| 2003 |
State MW, Greally JM, Cuker A, Bowers PN, Henegariu O, Morgan TM, Gunel M, DiLuna M, King RA, Nelson C, Donovan A, Anderson GM, Leckman JF, Hawkins T, Pauls DL, et al. Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype. Proceedings of the National Academy of Sciences of the United States of America. 100: 4684-9. PMID 12682296 DOI: 10.1073/Pnas.0730775100 |
0.783 |
|
| 2003 |
Pauls DL, Pulst SM, State MW. Genetics of Gilles de la Tourette Syndrome Genetics of Movement Disorders. 491-501. DOI: 10.1016/B978-012566652-7/50044-7 |
0.351 |
|
| 2001 |
Henegariu O, Grober L, Haskins W, Bowers PN, State MW, Ohmido N, Bray-Ward P, Ward DC. Rapid DNA fiber technique for size measurements of linear and circular DNA probes. Biotechniques. 31: 246-50. PMID 11515354 DOI: 10.2144/01312Bm01 |
0.401 |
|
| 2001 |
State MW, Pauls DL, Leckman JF. Tourette's syndrome and related disorders. Child and Adolescent Psychiatric Clinics of North America. 10: 317-31, ix. PMID 11351801 DOI: 10.1016/S1056-4993(18)30060-9 |
0.463 |
|
| 2000 |
State MW, Lombroso PJ, Pauls DL, Leckman JF. The genetics of childhood psychiatric disorders: a decade of progress. Journal of the American Academy of Child and Adolescent Psychiatry. 39: 946-62. PMID 10939224 DOI: 10.1097/00004583-200008000-00006 |
0.449 |
|
| 2000 |
State MW, Dykens EM. Genetics of childhood disorders: XV. Prader-Willi syndrome: genes, brain, and behavior. Journal of the American Academy of Child and Adolescent Psychiatry. 39: 797-800. PMID 10846317 DOI: 10.1097/00004583-200006000-00021 |
0.461 |
|
| 2000 |
Greally JM, State MW. Genetics of childhood disorders: XIII. Genomic imprinting: the indelible mark of the gamete. Journal of the American Academy of Child and Adolescent Psychiatry. 39: 532-5. PMID 10761358 DOI: 10.1097/00004583-200004000-00025 |
0.403 |
|
| 1999 |
Lin X, State MW, Vaccarino FM, Greally J, Hass M, Leckman JF. Identification, chromosomal assignment, and expression analysis of the human homeodomain-containing gene Orthopedia (OTP). Genomics. 60: 96-104. PMID 10458915 DOI: 10.1006/Geno.1999.5882 |
0.377 |
|
| 1999 |
Martin A, State M, Anderson GM, Kaye WM, Hanchett JM, McConaha CW, North WG, Leckman JF. Cerebrospinal fluid levels of oxytocin in Prader-Willi syndrome: a preliminary report. Biological Psychiatry. 44: 1349-52. PMID 9861478 DOI: 10.1016/S0006-3223(98)00190-5 |
0.443 |
|
| 1998 |
Leckman J, Schultz R, State M, Klin A, Gore J, Volkmar F. Genetics and neurobiology of autism: A modular approach European Neuropsychopharmacology. 8: S106. DOI: 10.1016/S0924-977X(98)80085-0 |
0.362 |
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