Literature DB >> 30901538

Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders.

Patrick F Sullivan1, Daniel H Geschwind2.   

Abstract

Studies of the genetics of psychiatric disorders have become one of the most exciting and fast-moving areas in human genetics. A decade ago, there were few reproducible findings, and now there are hundreds. In this review, we focus on the findings that have illuminated the genetic architecture of psychiatric disorders and the challenges of using these findings to inform our understanding of pathophysiology. The evidence is now overwhelming that psychiatric disorders are "polygenic"-that many genetic loci contribute to risk. With the exception of a subset of those with ASD, few individuals with a psychiatric disorder have a single, deterministic genetic cause; rather, developing a psychiatric disorder is influenced by hundreds of different genetic variants, consistent with a polygenic model. As progressively larger studies have uncovered more about their genetic architecture, the need to elucidate additional architectures has become clear. Even if we were to have complete knowledge of the genetic architecture of a psychiatric disorder, full understanding requires deep knowledge of the functional genomic architecture-the implicated loci impact regulatory processes that influence gene expression and the functional coordination of genes that control biological processes. Following from this is cellular architecture: of all brain regions, cell types, and developmental stages, where and when are the functional architectures operative? Given that the genetic architectures of different psychiatric disorders often strongly overlap, we are challenged to re-evaluate and refine the diagnostic architectures of psychiatric disorders using fundamental genetic and neurobiological data.
Copyright © 2019 Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 30901538      PMCID: PMC6432948          DOI: 10.1016/j.cell.2019.01.015

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  154 in total

Review 1.  Autism spectrum disorder: outcomes in adulthood.

Authors:  Patricia Howlin; Iliana Magiati
Journal:  Curr Opin Psychiatry       Date:  2017-03       Impact factor: 4.741

2.  An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people.

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Journal:  Science       Date:  2012-05-17       Impact factor: 47.728

3.  Enhancer-promoter interactions are encoded by complex genomic signatures on looping chromatin.

Authors:  Sean Whalen; Rebecca M Truty; Katherine S Pollard
Journal:  Nat Genet       Date:  2016-04-04       Impact factor: 38.330

Review 4.  Genomewide association studies: history, rationale, and prospects for psychiatric disorders.

Authors:  Sven Cichon; Nick Craddock; Mark Daly; Stephen V Faraone; Pablo V Gejman; John Kelsoe; Thomas Lehner; Douglas F Levinson; Audra Moran; Pamela Sklar; Patrick F Sullivan
Journal:  Am J Psychiatry       Date:  2009-04-01       Impact factor: 18.112

5.  Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.

Authors:  Christian R Marshall; Daniel P Howrigan; Daniele Merico; Bhooma Thiruvahindrapuram; Wenting Wu; Douglas S Greer; Danny Antaki; Aniket Shetty; Peter A Holmans; Dalila Pinto; Madhusudan Gujral; William M Brandler; Dheeraj Malhotra; Zhouzhi Wang; Karin V Fuentes Fajarado; Michelle S Maile; Stephan Ripke; Ingrid Agartz; Margot Albus; Madeline Alexander; Farooq Amin; Joshua Atkins; Silviu A Bacanu; Richard A Belliveau; Sarah E Bergen; Marcelo Bertalan; Elizabeth Bevilacqua; Tim B Bigdeli; Donald W Black; Richard Bruggeman; Nancy G Buccola; Randy L Buckner; Brendan Bulik-Sullivan; William Byerley; Wiepke Cahn; Guiqing Cai; Murray J Cairns; Dominique Campion; Rita M Cantor; Vaughan J Carr; Noa Carrera; Stanley V Catts; Kimberley D Chambert; Wei Cheng; C Robert Cloninger; David Cohen; Paul Cormican; Nick Craddock; Benedicto Crespo-Facorro; James J Crowley; David Curtis; Michael Davidson; Kenneth L Davis; Franziska Degenhardt; Jurgen Del Favero; Lynn E DeLisi; Dimitris Dikeos; Timothy Dinan; Srdjan Djurovic; Gary Donohoe; Elodie Drapeau; Jubao Duan; Frank Dudbridge; Peter Eichhammer; Johan Eriksson; Valentina Escott-Price; Laurent Essioux; Ayman H Fanous; Kai-How Farh; Martilias S Farrell; Josef Frank; Lude Franke; Robert Freedman; Nelson B Freimer; Joseph I Friedman; Andreas J Forstner; Menachem Fromer; Giulio Genovese; Lyudmila Georgieva; Elliot S Gershon; Ina Giegling; Paola Giusti-Rodríguez; Stephanie Godard; Jacqueline I Goldstein; Jacob Gratten; Lieuwe de Haan; Marian L Hamshere; Mark Hansen; Thomas Hansen; Vahram Haroutunian; Annette M Hartmann; Frans A Henskens; Stefan Herms; Joel N Hirschhorn; Per Hoffmann; Andrea Hofman; Hailiang Huang; Masashi Ikeda; Inge Joa; Anna K Kähler; René S Kahn; Luba Kalaydjieva; Juha Karjalainen; David Kavanagh; Matthew C Keller; Brian J Kelly; James L Kennedy; Yunjung Kim; James A Knowles; Bettina Konte; Claudine Laurent; Phil Lee; S Hong Lee; Sophie E Legge; Bernard Lerer; Deborah L Levy; Kung-Yee Liang; Jeffrey Lieberman; Jouko Lönnqvist; Carmel M Loughland; Patrik K E Magnusson; Brion S Maher; Wolfgang Maier; Jacques Mallet; Manuel Mattheisen; Morten Mattingsdal; Robert W McCarley; Colm McDonald; Andrew M McIntosh; Sandra Meier; Carin J Meijer; Ingrid Melle; Raquelle I Mesholam-Gately; Andres Metspalu; Patricia T Michie; Lili Milani; Vihra Milanova; Younes Mokrab; Derek W Morris; Bertram Müller-Myhsok; Kieran C Murphy; Robin M Murray; Inez Myin-Germeys; Igor Nenadic; Deborah A Nertney; Gerald Nestadt; Kristin K Nicodemus; Laura Nisenbaum; Annelie Nordin; Eadbhard O'Callaghan; Colm O'Dushlaine; Sang-Yun Oh; Ann Olincy; Line Olsen; F Anthony O'Neill; Jim Van Os; Christos Pantelis; George N Papadimitriou; Elena Parkhomenko; Michele T Pato; Tiina Paunio; Diana O Perkins; Tune H Pers; Olli Pietiläinen; Jonathan Pimm; Andrew J Pocklington; John Powell; Alkes Price; Ann E Pulver; Shaun M Purcell; Digby Quested; Henrik B Rasmussen; Abraham Reichenberg; Mark A Reimers; Alexander L Richards; Joshua L Roffman; Panos Roussos; Douglas M Ruderfer; Veikko Salomaa; Alan R Sanders; Adam Savitz; Ulrich Schall; Thomas G Schulze; Sibylle G Schwab; Edward M Scolnick; Rodney J Scott; Larry J Seidman; Jianxin Shi; Jeremy M Silverman; Jordan W Smoller; Erik Söderman; Chris C A Spencer; Eli A Stahl; Eric Strengman; Jana Strohmaier; T Scott Stroup; Jaana Suvisaari; Dragan M Svrakic; Jin P Szatkiewicz; Srinivas Thirumalai; Paul A Tooney; Juha Veijola; Peter M Visscher; John Waddington; Dermot Walsh; Bradley T Webb; Mark Weiser; Dieter B Wildenauer; Nigel M Williams; Stephanie Williams; Stephanie H Witt; Aaron R Wolen; Brandon K Wormley; Naomi R Wray; Jing Qin Wu; Clement C Zai; Rolf Adolfsson; Ole A Andreassen; Douglas H R Blackwood; Elvira Bramon; Joseph D Buxbaum; Sven Cichon; David A Collier; Aiden Corvin; Mark J Daly; Ariel Darvasi; Enrico Domenici; Tõnu Esko; Pablo V Gejman; Michael Gill; Hugh Gurling; Christina M Hultman; Nakao Iwata; Assen V Jablensky; Erik G Jönsson; Kenneth S Kendler; George Kirov; Jo Knight; Douglas F Levinson; Qingqin S Li; Steven A McCarroll; Andrew McQuillin; Jennifer L Moran; Bryan J Mowry; Markus M Nöthen; Roel A Ophoff; Michael J Owen; Aarno Palotie; Carlos N Pato; Tracey L Petryshen; Danielle Posthuma; Marcella Rietschel; Brien P Riley; Dan Rujescu; Pamela Sklar; David St Clair; James T R Walters; Thomas Werge; Patrick F Sullivan; Michael C O'Donovan; Stephen W Scherer; Benjamin M Neale; Jonathan Sebat
Journal:  Nat Genet       Date:  2016-11-21       Impact factor: 38.330

6.  Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

Authors:  Brian J O'Roak; Laura Vives; Santhosh Girirajan; Emre Karakoc; Niklas Krumm; Bradley P Coe; Roie Levy; Arthur Ko; Choli Lee; Joshua D Smith; Emily H Turner; Ian B Stanaway; Benjamin Vernot; Maika Malig; Carl Baker; Beau Reilly; Joshua M Akey; Elhanan Borenstein; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Jay Shendure; Evan E Eichler
Journal:  Nature       Date:  2012-04-04       Impact factor: 49.962

7.  Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.

Authors:  Maja Bucan; Brett S Abrahams; Kai Wang; Joseph T Glessner; Edward I Herman; Lisa I Sonnenblick; Ana I Alvarez Retuerto; Marcin Imielinski; Dexter Hadley; Jonathan P Bradfield; Cecilia Kim; Nicole B Gidaya; Ingrid Lindquist; Ted Hutman; Marian Sigman; Vlad Kustanovich; Clara M Lajonchere; Andrew Singleton; Junhyong Kim; Thomas H Wassink; William M McMahon; Thomas Owley; John A Sweeney; Hilary Coon; John I Nurnberger; Mingyao Li; Rita M Cantor; Nancy J Minshew; James S Sutcliffe; Edwin H Cook; Geraldine Dawson; Joseph D Buxbaum; Struan F A Grant; Gerard D Schellenberg; Daniel H Geschwind; Hakon Hakonarson
Journal:  PLoS Genet       Date:  2009-06-26       Impact factor: 5.917

8.  Most genetic risk for autism resides with common variation.

Authors:  Trent Gaugler; Lambertus Klei; Stephan J Sanders; Corneliu A Bodea; Arthur P Goldberg; Ann B Lee; Milind Mahajan; Dina Manaa; Yudi Pawitan; Jennifer Reichert; Stephan Ripke; Sven Sandin; Pamela Sklar; Oscar Svantesson; Abraham Reichenberg; Christina M Hultman; Bernie Devlin; Kathryn Roeder; Joseph D Buxbaum
Journal:  Nat Genet       Date:  2014-07-20       Impact factor: 38.330

9.  Damaging de novo mutations diminish motor skills in children on the autism spectrum.

Authors:  Andreas Buja; Natalia Volfovsky; Abba M Krieger; Catherine Lord; Alex E Lash; Michael Wigler; Ivan Iossifov
Journal:  Proc Natl Acad Sci U S A       Date:  2018-02-06       Impact factor: 11.205

10.  Rare and low-frequency coding variants alter human adult height.

Authors:  Eirini Marouli; Mariaelisa Graff; Carolina Medina-Gomez; Ken Sin Lo; Andrew R Wood; Troels R Kjaer; Rebecca S Fine; Yingchang Lu; Claudia Schurmann; Heather M Highland; Sina Rüeger; Gudmar Thorleifsson; Anne E Justice; David Lamparter; Kathleen E Stirrups; Valérie Turcot; Kristin L Young; Thomas W Winkler; Tõnu Esko; Tugce Karaderi; Adam E Locke; Nicholas G D Masca; Maggie C Y Ng; Poorva Mudgal; Manuel A Rivas; Sailaja Vedantam; Anubha Mahajan; Xiuqing Guo; Goncalo Abecasis; Katja K Aben; Linda S Adair; Dewan S Alam; Eva Albrecht; Kristine H Allin; Matthew Allison; Philippe Amouyel; Emil V Appel; Dominique Arveiler; Folkert W Asselbergs; Paul L Auer; Beverley Balkau; Bernhard Banas; Lia E Bang; Marianne Benn; Sven Bergmann; Lawrence F Bielak; Matthias Blüher; Heiner Boeing; Eric Boerwinkle; Carsten A Böger; Lori L Bonnycastle; Jette Bork-Jensen; Michiel L Bots; Erwin P Bottinger; Donald W Bowden; Ivan Brandslund; Gerome Breen; Murray H Brilliant; Linda Broer; Amber A Burt; Adam S Butterworth; David J Carey; Mark J Caulfield; John C Chambers; Daniel I Chasman; Yii-Der Ida Chen; Rajiv Chowdhury; Cramer Christensen; Audrey Y Chu; Massimiliano Cocca; Francis S Collins; James P Cook; Janie Corley; Jordi Corominas Galbany; Amanda J Cox; Gabriel Cuellar-Partida; John Danesh; Gail Davies; Paul I W de Bakker; Gert J de Borst; Simon de Denus; Mark C H de Groot; Renée de Mutsert; Ian J Deary; George Dedoussis; Ellen W Demerath; Anneke I den Hollander; Joe G Dennis; Emanuele Di Angelantonio; Fotios Drenos; Mengmeng Du; Alison M Dunning; Douglas F Easton; Tapani Ebeling; Todd L Edwards; Patrick T Ellinor; Paul Elliott; Evangelos Evangelou; Aliki-Eleni Farmaki; Jessica D Faul; Mary F Feitosa; Shuang Feng; Ele Ferrannini; Marco M Ferrario; Jean Ferrieres; Jose C Florez; Ian Ford; Myriam Fornage; Paul W Franks; Ruth Frikke-Schmidt; Tessel E Galesloot; Wei Gan; Ilaria Gandin; Paolo Gasparini; Vilmantas Giedraitis; Ayush Giri; Giorgia Girotto; Scott D Gordon; Penny Gordon-Larsen; Mathias Gorski; Niels Grarup; Megan L Grove; Vilmundur Gudnason; Stefan Gustafsson; Torben Hansen; Kathleen Mullan Harris; Tamara B Harris; Andrew T Hattersley; Caroline Hayward; Liang He; Iris M Heid; Kauko Heikkilä; Øyvind Helgeland; Jussi Hernesniemi; Alex W Hewitt; Lynne J Hocking; Mette Hollensted; Oddgeir L Holmen; G Kees Hovingh; Joanna M M Howson; Carel B Hoyng; Paul L Huang; Kristian Hveem; M Arfan Ikram; Erik Ingelsson; Anne U Jackson; Jan-Håkan Jansson; Gail P Jarvik; Gorm B Jensen; Min A Jhun; Yucheng Jia; Xuejuan Jiang; Stefan Johansson; Marit E Jørgensen; Torben Jørgensen; Pekka Jousilahti; J Wouter Jukema; Bratati Kahali; René S Kahn; Mika Kähönen; Pia R Kamstrup; Stavroula Kanoni; Jaakko Kaprio; Maria Karaleftheri; Sharon L R Kardia; Fredrik Karpe; Frank Kee; Renske Keeman; Lambertus A Kiemeney; Hidetoshi Kitajima; Kirsten B Kluivers; Thomas Kocher; Pirjo Komulainen; Jukka Kontto; Jaspal S Kooner; Charles Kooperberg; Peter Kovacs; Jennifer Kriebel; Helena Kuivaniemi; Sébastien Küry; Johanna Kuusisto; Martina La Bianca; Markku Laakso; Timo A Lakka; Ethan M Lange; Leslie A Lange; Carl D Langefeld; Claudia Langenberg; Eric B Larson; I-Te Lee; Terho Lehtimäki; Cora E Lewis; Huaixing Li; Jin Li; Ruifang Li-Gao; Honghuang Lin; Li-An Lin; Xu Lin; Lars Lind; Jaana Lindström; Allan Linneberg; Yeheng Liu; Yongmei Liu; Artitaya Lophatananon; Jian'an Luan; Steven A Lubitz; Leo-Pekka Lyytikäinen; David A Mackey; Pamela A F Madden; Alisa K Manning; Satu Männistö; Gaëlle Marenne; Jonathan Marten; Nicholas G Martin; Angela L Mazul; Karina Meidtner; Andres Metspalu; Paul Mitchell; Karen L Mohlke; Dennis O Mook-Kanamori; Anna Morgan; Andrew D Morris; Andrew P Morris; Martina Müller-Nurasyid; Patricia B Munroe; Mike A Nalls; Matthias Nauck; Christopher P Nelson; Matt Neville; Sune F Nielsen; Kjell Nikus; Pål R Njølstad; Børge G Nordestgaard; Ioanna Ntalla; Jeffrey R O'Connel; Heikki Oksa; Loes M Olde Loohuis; Roel A Ophoff; Katharine R Owen; Chris J Packard; Sandosh Padmanabhan; Colin N A Palmer; Gerard Pasterkamp; Aniruddh P Patel; Alison Pattie; Oluf Pedersen; Peggy L Peissig; Gina M Peloso; Craig E Pennell; Markus Perola; James A Perry; John R B Perry; Thomas N Person; Ailith Pirie; Ozren Polasek; Danielle Posthuma; Olli T Raitakari; Asif Rasheed; Rainer Rauramaa; Dermot F Reilly; Alex P Reiner; Frida Renström; Paul M Ridker; John D Rioux; Neil Robertson; Antonietta Robino; Olov Rolandsson; Igor Rudan; Katherine S Ruth; Danish Saleheen; Veikko Salomaa; Nilesh J Samani; Kevin Sandow; Yadav Sapkota; Naveed Sattar; Marjanka K Schmidt; Pamela J Schreiner; Matthias B Schulze; Robert A Scott; Marcelo P Segura-Lepe; Svati Shah; Xueling Sim; Suthesh Sivapalaratnam; Kerrin S Small; Albert Vernon Smith; Jennifer A Smith; Lorraine Southam; Timothy D Spector; Elizabeth K Speliotes; John M Starr; Valgerdur Steinthorsdottir; Heather M Stringham; Michael Stumvoll; Praveen Surendran; Leen M 't Hart; Katherine E Tansey; Jean-Claude Tardif; Kent D Taylor; Alexander Teumer; Deborah J Thompson; Unnur Thorsteinsdottir; Betina H Thuesen; Anke Tönjes; Gerard Tromp; Stella Trompet; Emmanouil Tsafantakis; Jaakko Tuomilehto; Anne Tybjaerg-Hansen; Jonathan P Tyrer; Rudolf Uher; André G Uitterlinden; Sheila Ulivi; Sander W van der Laan; Andries R Van Der Leij; Cornelia M van Duijn; Natasja M van Schoor; Jessica van Setten; Anette Varbo; Tibor V Varga; Rohit Varma; Digna R Velez Edwards; Sita H Vermeulen; Henrik Vestergaard; Veronique Vitart; Thomas F Vogt; Diego Vozzi; Mark Walker; Feijie Wang; Carol A Wang; Shuai Wang; Yiqin Wang; Nicholas J Wareham; Helen R Warren; Jennifer Wessel; Sara M Willems; James G Wilson; Daniel R Witte; Michael O Woods; Ying Wu; Hanieh Yaghootkar; Jie Yao; Pang Yao; Laura M Yerges-Armstrong; Robin Young; Eleftheria Zeggini; Xiaowei Zhan; Weihua Zhang; Jing Hua Zhao; Wei Zhao; Wei Zhao; He Zheng; Wei Zhou; Jerome I Rotter; Michael Boehnke; Sekar Kathiresan; Mark I McCarthy; Cristen J Willer; Kari Stefansson; Ingrid B Borecki; Dajiang J Liu; Kari E North; Nancy L Heard-Costa; Tune H Pers; Cecilia M Lindgren; Claus Oxvig; Zoltán Kutalik; Fernando Rivadeneira; Ruth J F Loos; Timothy M Frayling; Joel N Hirschhorn; Panos Deloukas; Guillaume Lettre
Journal:  Nature       Date:  2017-02-01       Impact factor: 49.962

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  91 in total

Review 1.  Disentangling chromatin architecture to gain insights into the etiology of brain disorders.

Authors:  Janine M Lamonica; Zhaolan Zhou
Journal:  Curr Opin Genet Dev       Date:  2019-07-16       Impact factor: 5.578

Review 2.  Integrating CRISPR Engineering and hiPSC-Derived 2D Disease Modeling Systems.

Authors:  Kristina Rehbach; Michael B Fernando; Kristen J Brennand
Journal:  J Neurosci       Date:  2020-02-05       Impact factor: 6.167

3.  Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits.

Authors:  Amanda K Tilot; Arianna Vino; Katerina S Kucera; Duncan A Carmichael; Loes van den Heuvel; Joery den Hoed; Anton V Sidoroff-Dorso; Archie Campbell; David J Porteous; Beate St Pourcain; Tessa M van Leeuwen; Jamie Ward; Romke Rouw; Julia Simner; Simon E Fisher
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2019-10-21       Impact factor: 6.237

Review 4.  Functional genomics links genetic origins to pathophysiology in neurodegenerative and neuropsychiatric disease.

Authors:  Brie Wamsley; Daniel H Geschwind
Journal:  Curr Opin Genet Dev       Date:  2020-07-04       Impact factor: 5.578

Review 5.  Structural variation in the sequencing era.

Authors:  Steve S Ho; Alexander E Urban; Ryan E Mills
Journal:  Nat Rev Genet       Date:  2019-11-15       Impact factor: 53.242

6.  Brief Report: Genetic Links Between Autism and Suicidal Behavior-A Preliminary Investigation.

Authors:  Emily DiBlasi; Anne V Kirby; Eoin Gaj; Anna R Docherty; Brooks R Keeshin; Amanda V Bakian; Hilary Coon
Journal:  J Autism Dev Disord       Date:  2020-10

7.  Human CRY1 variants associate with attention deficit/hyperactivity disorder.

Authors:  O Emre Onat; M Ece Kars; Şeref Gül; Kaya Bilguvar; Yiming Wu; Ayşe Özhan; Cihan Aydın; A Nazlı Başak; M Allegra Trusso; Arianna Goracci; Chiara Fallerini; Alessandra Renieri; Jean-Laurent Casanova; Yuval Itan; Cem E Atbaşoğlu; Meram C Saka; İ Halil Kavaklı; Tayfun Özçelik
Journal:  J Clin Invest       Date:  2020-07-01       Impact factor: 14.808

Review 8.  Polygenic risk score as clinical utility in psychiatry: a clinical viewpoint.

Authors:  Masashi Ikeda; Takeo Saito; Tetsufumi Kanazawa; Nakao Iwata
Journal:  J Hum Genet       Date:  2020-08-07       Impact factor: 3.172

Review 9.  Uncovering the Genetic Architecture of Major Depression.

Authors:  Andrew M McIntosh; Patrick F Sullivan; Cathryn M Lewis
Journal:  Neuron       Date:  2019-04-03       Impact factor: 17.173

10.  Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium.

Authors:  Renato Polimanti; Raymond K Walters; Emma C Johnson; Jeanette N McClintick; Amy E Adkins; Daniel E Adkins; Silviu-Alin Bacanu; Laura J Bierut; Tim B Bigdeli; Sandra Brown; Kathleen K Bucholz; William E Copeland; E Jane Costello; Louisa Degenhardt; Lindsay A Farrer; Tatiana M Foroud; Louis Fox; Alison M Goate; Richard Grucza; Laura M Hack; Dana B Hancock; Sarah M Hartz; Andrew C Heath; John K Hewitt; Christian J Hopfer; Eric O Johnson; Kenneth S Kendler; Henry R Kranzler; Kenneth Krauter; Dongbing Lai; Pamela A F Madden; Nicholas G Martin; Hermine H Maes; Elliot C Nelson; Roseann E Peterson; Bernice Porjesz; Brien P Riley; Nancy Saccone; Michael Stallings; Tamara L Wall; Bradley T Webb; Leah Wetherill; Howard J Edenberg; Arpana Agrawal; Joel Gelernter
Journal:  Mol Psychiatry       Date:  2020-02-26       Impact factor: 15.992

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