Jakob Grove

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David HougaardDirector Department for Congenital Disorders, Statens Serum InstitutVerified email at ssi.dk
Thomas WergeDirector, Professor, RHP-Institute of Biological Psychiatry & University of CopenhagenVerified email at regionh.dk
Jonas Bybjerg-GrauholmStatens Serum insitutVerified email at ssi.dk
Ditte DemontisLektor i medicinsk genetik, Biomedicin, Aarhus UniveristetVerified email at hum-gen.au.dk
Benjamin NealeMassachusetts General Hospital; Broad Institute; Harvard Medical SchoolVerified email at broadinstitute.org
Elise RobinsonAssistant Professor of Psychiatry, Massachusetts General Hospital and Harvard Medical SchoolVerified email at broadinstitute.org
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteVerified email at atgu.mgh.harvard.edu
Naomi WrayUniversity of QueenslandVerified email at uq.edu.au
Bent Norgaard PedersenConsultant, Prof. emeritus, MD,DMSc Statens Serum Institute,DenmarkVerified email at ssi.dk
Mads Vilhelm HollegaardSection of Neonatal Genetics, Dept. Congenital Disorders, Statens Serum InstitutVerified email at ssi.dk
Erik Lykke MortensenUniversity of CpopenhagenVerified email at sund.ku.dk
Manuel MattheisenDalhousie UniversityVerified email at dal.ca
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité - Universitätsmedizin BerlinVerified email at charite.de
Verneri AnttilaPost-doctoral Fellow, Broad Institute / Harvard Medical SchoolVerified email at atgu.mgh.harvard.edu
Mette NyegaardProfessor and Director Department Congenital Disorders, Statens Serum InstitutVerified email at ssi.dk
Brendan Bulik-SullivanGVVerified email at gv.com
Francesco LescaiAssociate Professor of Bioinformatics, University of PaviaVerified email at unipv.it
Alexander (Sasha) GusevDana-Farber Cancer InstituteVerified email at dfci.harvard.edu
Po-Ru LohBrigham and Women's Hospital / Harvard Medical SchoolVerified email at broadinstitute.org
Bo JacobssonSahlgrenska University HospitalVerified email at obgyn.gu.se

Jakob Grove

Professor, Department of Biomedicine, Aarhus University

Verified email at biomed.au.dk

Bioinformatics statistics genetics psychiatry epidemiology


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ... Nature genetics 50 (5), 668-681, 2018	2844	2018
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	2335	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	2274	2019
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions DM Howard, MJ Adams, TK Clarke, JD Hafferty, J Gibson, M Shirali, ... Nature neuroscience 22 (3), 343-352, 2019	2248	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	2064	2020
Mapping genomic loci implicates genes and synaptic biology in schizophrenia V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ... Nature 604 (7906), 502-508, 2022	1748	2022
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection AF Pardiñas, P Holmans, AJ Pocklington, V Escott-Price, S Ripke, ... Nature genetics 50 (3), 381-389, 2018	1628	2018
Genome-wide association study identifies 30 loci associated with bipolar disorder EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ... Nature genetics 51 (5), 793-803, 2019	1509	2019
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1484	2018
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores BJ Vilhjálmsson, J Yang, H Finucane, A Gusev, S Lindström, S Ripke, ... American Journal of Human Genetics 97 (4), 576–592, 2015	1452	2015
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ... Cell 179 (7), 1469-1482. e11, 2019	1186	2019
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology N Mullins, AJ Forstner, KS O’Connell, B Coombes, JRI Coleman, Z Qiao, ... Nature genetics 53 (6), 817-829, 2021	1077	2021
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types HK Finucane, YA Reshef, V Anttila, K Slowikowski, A Gusev, A Byrnes, ... Nature genetics 50 (4), 621-629, 2018	979	2018
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa HJ Watson, Z Yilmaz, LM Thornton, C Hübel, JRI Coleman, HA Gaspar, ... Nature genetics 51 (8), 1207-1214, 2019	965	2019
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), 978-985, 2017	836*	2017
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), 2018	702	2018
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ... Am J Hum Genet 95 (5), 535–552, 2014	685	2014
Assessment of bidirectional relationships between physical activity and depression among adults: a 2-sample Mendelian randomization study KW Choi, CY Chen, MB Stein, YC Klimentidis, MJ Wang, KC Koenen, ... JAMA psychiatry 76 (4), 399-408, 2019	615	2019
Genetic identification of brain cell types underlying schizophrenia NG Skene, J Bryois, TE Bakken, G Breen, JJ Crowley, HA Gaspar, ... Nature genetics 50 (6), 825-833, 2018	608	2018
Rare coding variants in ten genes confer substantial risk for schizophrenia T Singh, T Poterba, D Curtis, H Akil, M Al Eissa, JD Barchas, N Bass, ... Nature 604 (7906), 509-516, 2022	605	2022

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