Elise Robinson

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	Wszystkie	Od 2020
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Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteZweryfikowany adres z atgu.mgh.harvard.edu
Benjamin NealeMassachusetts General Hospital; Broad Institute; Harvard Medical SchoolZweryfikowany adres z broadinstitute.org
Verneri AnttilaPost-doctoral Fellow, Broad Institute / Harvard Medical SchoolZweryfikowany adres z atgu.mgh.harvard.edu
Stephan J. SandersProfessor, Oxford and UCSFZweryfikowany adres z ucsf.edu
Brendan Bulik-SullivanGVZweryfikowany adres z gv.com
Angelica RonaldProfessor of Psychology and Genetics, Faculty of Health and Medical Sciences, University of SurreyZweryfikowany adres z surrey.ac.uk
Jack A. KosmickiRegeneron Genetics CenterZweryfikowany adres z fas.harvard.edu
Francesca HappeMRC SGDP Centre, Institute of Psychiatry, King's College LondonZweryfikowany adres z kcl.ac.uk
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité - Universitätsmedizin BerlinZweryfikowany adres z charite.de
Kaitlin E. SamochaMassachusetts General HospitalZweryfikowany adres z partners.org
Daniel HowriganGroup LeaderZweryfikowany adres z broadinstitute.org
Roy PerlisMassachusetts General HospitalZweryfikowany adres z mgh.harvard.edu
Lauren M. McGrathUniversity of DenverZweryfikowany adres z du.edu
Ruben GurUniversity of Pennsylvania Zweryfikowany adres z upenn.edu
Caitlin C ClementsUniversity of Notre DameZweryfikowany adres z nd.edu
Daniel G MacArthurGarvan Institute of Medical Research, Murdoch Children's Research InstituteZweryfikowany adres z garvan.org.au
Mark TaylorPrincipal Researcher at Department of Medical Epidemiology & Biostatistics, Karolinska InstitutetZweryfikowany adres z ki.se
Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNZweryfikowany adres z email.chop.edu
Jian YangProfessor of Statistical Genetics, Westlake UniversityZweryfikowany adres z westlake.edu.cn
Patrick F SullivanProfessor of Genetics, University of North Carolina; Professor, MEB, Karolinska InstitutetZweryfikowany adres z med.unc.edu

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Elise Robinson

Assistant Professor of Psychiatry, Massachusetts General Hospital and Harvard Medical School

Zweryfikowany adres z broadinstitute.org - Strona główna

Neuropsychiatric disorders genetics


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
An atlas of genetic correlations across human diseases and traits B Bulik-Sullivan, HK Finucane, V Anttila, A Gusev, FR Day, PR Loh, ... Nature genetics 47 (11), 1236-1241, 2015	4033	2015
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ... Nature genetics 51 (1), 63-75, 2019	2364	2019
Identification of common genetic risk variants for autism spectrum disorder J Grove, S Ripke, TD Als, M Mattheisen, RK Walters, H Won, J Pallesen, ... Nature genetics 51 (3), 431-444, 2019	2196	2019
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ... Cell 180 (3), 568-584. e23, 2020	2054	2020
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ... Neuron 87 (6), 1215-1233, 2015	1598	2015
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1557	2018
A framework for the interpretation of de novo mutation in human disease KE Samocha, EB Robinson, SJ Sanders, C Stevens, A Sabo, LM McGrath, ... Nature genetics 46 (9), 944-950, 2014	1152	2014
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), eaap8757, 2018	720	2018
Examining and interpreting the female protective effect against autistic behavior EB Robinson, P Lichtenstein, H Anckarsäter, F Happé, A Ronald Proceedings of the National Academy of Sciences 110 (13), 5258-5262, 2013	604	2013
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia Molecular autism 8, 1-17, 2017	548	2017
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ... Nature genetics 49 (7), 978, 2017	505	2017
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ... Nature genetics 48 (5), 552-555, 2016	455	2016
Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%) EB Robinson, KC Koenen, MC McCormick, K Munir, V Hallett, F Happé, ... Archives of general psychiatry 68 (11), 1113-1121, 2011	392	2011
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples JA Kosmicki, KE Samocha, DP Howrigan, SJ Sanders, K Slowikowski, ... Nature genetics 49 (4), 504-510, 2017	363	2017
In vivo Perturb-Seq reveals neuronal and glial abnormalities associated with autism risk genes X Jin, SK Simmons, A Guo, AS Shetty, M Ko, L Nguyen, V Jokhi, ... Science 370 (6520), eaaz6063, 2020	269	2020
Predicting polygenic risk of psychiatric disorders AR Martin, MJ Daly, EB Robinson, SE Hyman, BM Neale Biological psychiatry 86 (2), 97-109, 2019	264	2019
Prenatal antidepressant exposure is associated with risk for attention-deficit hyperactivity disorder but not autism spectrum disorder in a large health system CC Clements, VM Castro, SR Blumenthal, HR Rosenfield, SN Murphy, ... Molecular psychiatry 20 (6), 727-734, 2015	252	2015
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants FK Satterstrom, RK Walters, T Singh, EM Wigdor, F Lescai, D Demontis, ... Nature neuroscience 22 (12), 1961-1965, 2019	240	2019
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ... Biological psychiatry 83 (12), 1044-1053, 2018	202	2018
Tumor cell-derived extracellular vesicle-coated nanocarriers: an efficient theranostic platform for the cancer-specific delivery of anti-miR-21 and imaging agents R JC Bose, S Uday Kumar, Y Zeng, R Afjei, E Robinson, K Lau, ... ACS nano 12 (11), 10817-10832, 2018	201	2018

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