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Donna M. Werling, B.S. - Publications

Affiliations: 
University of California, Los Angeles, Los Angeles, CA 
Area:
Neurogenetics, Autism
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30 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
2024 Kim SW, Lee H, Song DY, Lee GH, Ji J, Park JW, Han JH, Lee JW, Byun HJ, Son JH, Kim YR, Lee Y, Kim J, Jung A, Lee J, ... ... Werling DM, et al. Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism. Genome Medicine. 16: 114. PMID 39334436 DOI: 10.1186/s13073-024-01385-6  0.383
2024 Kim Y, Jeong M, Koh IG, Kim C, Lee H, Kim JH, Yurko R, Kim IB, Park J, Werling DM, Sanders SJ, An JY. CWAS-Plus: estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. Briefings in Bioinformatics. 25. PMID 38966948 DOI: 10.1093/bib/bbae323  0.814
2024 Kissel LT, Pochareddy S, An JY, Sestan N, Sanders SJ, Wang X, Werling DM. Sex-Differential Gene Expression in Developing Human Cortex and Its Intersection With Autism Risk Pathways. Biological Psychiatry Global Open Science. 4: 100321. PMID 38957312 DOI: 10.1016/j.bpsgos.2024.100321  0.776
2024 Kim Y, Jeong M, Koh IG, Kim C, Lee H, Kim JH, Yurko R, Kim IB, Park J, Werling DM, Sanders SJ, An JY. CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. Medrxiv : the Preprint Server For Health Sciences. PMID 38699372 DOI: 10.1101/2024.04.15.24305828  0.822
2021 Liang L, Fazel Darbandi S, Pochareddy S, Gulden FO, Gilson MC, Sheppard BK, Sahagun A, An JY, Werling DM, Rubenstein JLR, Sestan N, Bender KJ, Sanders SJ. Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain. Genome Medicine. 13: 135. PMID 34425903 DOI: 10.1186/s13073-021-00949-0  0.753
2020 Kissel LT, Werling DM. Neural Transcriptomic Analysis of Sex Differences in Autism Spectrum Disorder: Current Insights and Future Directions. Biological Psychiatry. PMID 33551190 DOI: 10.1016/j.biopsych.2020.11.023  0.389
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, 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  0.81
2019 Werling DM. Clinically Defined Subtypes of Bipolar Disorder Are Reflected in Genomic Architecture. Biological Psychiatry. 86: 78-80. PMID 31272529 DOI: 10.1016/J.Biopsych.2019.05.010  0.51
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  0.79
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  0.84
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  0.846
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, 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  0.819
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, 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  0.779
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, 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  0.785
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, et al. Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. PMID 29549319 DOI: 10.1038/S41593-018-0102-8  0.76
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, 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  0.801
2017 Grzadzinski R, Lord C, Sanders SJ, Werling D, Bal VH. Children with autism spectrum disorder who improve with fever: Insights from the Simons Simplex Collection. Autism Research : Official Journal of the International Society For Autism Research. PMID 28861935 DOI: 10.1002/Aur.1856  0.685
2017 Bishop SL, Farmer C, Bal V, Robinson EB, Willsey AJ, Werling DM, Havdahl KA, Sanders SJ, Thurm A. Identification of Developmental and Behavioral Markers Associated With Genetic Abnormalities in Autism Spectrum Disorder. The American Journal of Psychiatry. appiajp201716101115. PMID 28253736 DOI: 10.1176/Appi.Ajp.2017.16101115  0.773
2016 Werling DM. The role of sex-differential biology in risk for autism spectrum disorder. Biology of Sex Differences. 7: 58. PMID 27891212 DOI: 10.1186/S13293-016-0112-8  0.386
2016 Werling DM, Parikshak NN, Geschwind DH. Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders. Nature Communications. 7: 10717. PMID 26892004 DOI: 10.1038/Ncomms10717  0.748
2016 Werling DM, Sanders SJ. Gene coexpression modules in human cognition. Nature Neuroscience. 19: 173-5. PMID 26814582 DOI: 10.1038/Nn.4226  0.72
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, ... ... Werling DM, et al. The PsychENCODE project. Nature Neuroscience. 18: 1707-1712. PMID 26605881 DOI: 10.1038/Nn.4156  0.793
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, ... ... Werling DM, et al. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 87: 1215-1233. PMID 26402605 DOI: 10.1016/J.Neuron.2015.09.016  0.799
2015 Werling DM, Geschwind DH. Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins. Molecular Autism. 6: 27. PMID 25973164 DOI: 10.1186/S13229-015-0004-5  0.505
2015 Lowe JK, Werling DM, Constantino JN, Cantor RM, Geschwind DH. Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8. The American Journal of Psychiatry. 172: 266-75. PMID 25727539 DOI: 10.1176/Appi.Ajp.2014.14050576  0.567
2015 Werling DM, Geschwind DH. Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins Molecular Autism. DOI: 10.1186/s13229-015-0004-5  0.477
2014 Oguro-Ando A, Rosensweig C, Herman E, Nishimura Y, Werling D, Bill BR, Berg JM, Gao F, Coppola G, Abrahams BS, Geschwind DH. Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR. Molecular Psychiatry. PMID 25311365 DOI: 10.1038/Mp.2014.124  0.781
2014 Werling DM, Lowe JK, Luo R, Cantor RM, Geschwind DH. Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder. Molecular Autism. 5: 13. PMID 24533643 DOI: 10.1186/2040-2392-5-13  0.668
2013 Werling DM, Geschwind DH. Understanding sex bias in autism spectrum disorder. Proceedings of the National Academy of Sciences of the United States of America. 110: 4868-9. PMID 23476067 DOI: 10.1073/Pnas.1301602110  0.525
2013 Werling DM, Geschwind DH. Sex differences in autism spectrum disorders. Current Opinion in Neurology. 26: 146-53. PMID 23406909 DOI: 10.1097/Wco.0B013E32835Ee548  0.549
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