Literature DB >> 27021940

Rare genetic variants and schizophrenia.

Jonathan Flint1.   

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Year:  2016        PMID: 27021940     DOI: 10.1038/nn.4271

Source DB:  PubMed          Journal:  Nat Neurosci        ISSN: 1097-6256            Impact factor:   24.884


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  14 in total

1.  Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene.

Authors:  Atsushi Takata; Bin Xu; Iuliana Ionita-Laza; J Louw Roos; Joseph A Gogos; Maria Karayiorgou
Journal:  Neuron       Date:  2014-05-21       Impact factor: 17.173

2.  Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.

Authors:  E M Kenny; P Cormican; S Furlong; E Heron; G Kenny; C Fahey; E Kelleher; S Ennis; D Tropea; R Anney; A P Corvin; G Donohoe; L Gallagher; M Gill; D W Morris
Journal:  Mol Psychiatry       Date:  2013-10-15       Impact factor: 15.992

3.  Searching for missing heritability: designing rare variant association studies.

Authors:  Or Zuk; Stephen F Schaffner; Kaitlin Samocha; Ron Do; Eliana Hechter; Sekar Kathiresan; Mark J Daly; Benjamin M Neale; Shamil R Sunyaev; Eric S Lander
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-17       Impact factor: 11.205

4.  Increased exonic de novo mutation rate in individuals with schizophrenia.

Authors:  Simon L Girard; Julie Gauthier; Anne Noreau; Lan Xiong; Sirui Zhou; Loubna Jouan; Alexandre Dionne-Laporte; Dan Spiegelman; Edouard Henrion; Ousmane Diallo; Pascale Thibodeau; Isabelle Bachand; Jessie Y J Bao; Amy Hin Yan Tong; Chi-Ho Lin; Bruno Millet; Nematollah Jaafari; Ridha Joober; Patrick A Dion; Si Lok; Marie-Odile Krebs; Guy A Rouleau
Journal:  Nat Genet       Date:  2011-07-10       Impact factor: 38.330

5.  FTO Obesity Variant Circuitry and Adipocyte Browning in Humans.

Authors:  Melina Claussnitzer; Simon N Dankel; Kyoung-Han Kim; Gerald Quon; Wouter Meuleman; Christine Haugen; Viktoria Glunk; Isabel S Sousa; Jacqueline L Beaudry; Vijitha Puviindran; Nezar A Abdennur; Jannel Liu; Per-Arne Svensson; Yi-Hsiang Hsu; Daniel J Drucker; Gunnar Mellgren; Chi-Chung Hui; Hans Hauner; Manolis Kellis
Journal:  N Engl J Med       Date:  2015-08-19       Impact factor: 91.245

6.  A systematic survey of loss-of-function variants in human protein-coding genes.

Authors:  Daniel G MacArthur; Suganthi Balasubramanian; Adam Frankish; Ni Huang; James Morris; Klaudia Walter; Luke Jostins; Lukas Habegger; Joseph K Pickrell; Stephen B Montgomery; Cornelis A Albers; Zhengdong D Zhang; Donald F Conrad; Gerton Lunter; Hancheng Zheng; Qasim Ayub; Mark A DePristo; Eric Banks; Min Hu; Robert E Handsaker; Jeffrey A Rosenfeld; Menachem Fromer; Mike Jin; Xinmeng Jasmine Mu; Ekta Khurana; Kai Ye; Mike Kay; Gary Ian Saunders; Marie-Marthe Suner; Toby Hunt; If H A Barnes; Clara Amid; Denise R Carvalho-Silva; Alexandra H Bignell; Catherine Snow; Bryndis Yngvadottir; Suzannah Bumpstead; David N Cooper; Yali Xue; Irene Gallego Romero; Jun Wang; Yingrui Li; Richard A Gibbs; Steven A McCarroll; Emmanouil T Dermitzakis; Jonathan K Pritchard; Jeffrey C Barrett; Jennifer Harrow; Matthew E Hurles; Mark B Gerstein; Chris Tyler-Smith
Journal:  Science       Date:  2012-02-17       Impact factor: 47.728

7.  A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.

Authors:  Timothy M Frayling; Nicholas J Timpson; Michael N Weedon; Eleftheria Zeggini; Rachel M Freathy; Cecilia M Lindgren; John R B Perry; Katherine S Elliott; Hana Lango; Nigel W Rayner; Beverley Shields; Lorna W Harries; Jeffrey C Barrett; Sian Ellard; Christopher J Groves; Bridget Knight; Ann-Marie Patch; Andrew R Ness; Shah Ebrahim; Debbie A Lawlor; Susan M Ring; Yoav Ben-Shlomo; Marjo-Riitta Jarvelin; Ulla Sovio; Amanda J Bennett; David Melzer; Luigi Ferrucci; Ruth J F Loos; Inês Barroso; Nicholas J Wareham; Fredrik Karpe; Katharine R Owen; Lon R Cardon; Mark Walker; Graham A Hitman; Colin N A Palmer; Alex S F Doney; Andrew D Morris; George Davey Smith; Andrew T Hattersley; Mark I McCarthy
Journal:  Science       Date:  2007-04-12       Impact factor: 47.728

8.  A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing.

Authors:  X Hu; B Zhang; W Liu; S Paciga; W He; T A Lanz; R Kleiman; B Dougherty; S K Hall; A M McIntosh; S M Lawrie; A Power; S L John; D Blackwood; D St Clair; N J Brandon
Journal:  Mol Psychiatry       Date:  2013-10-15       Impact factor: 15.992

9.  Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

Authors:  Tarjinder Singh; Mitja I Kurki; David Curtis; Shaun M Purcell; Lucy Crooks; Jeremy McRae; Jaana Suvisaari; Himanshu Chheda; Douglas Blackwood; Gerome Breen; Olli Pietiläinen; Sebastian S Gerety; Muhammad Ayub; Moira Blyth; Trevor Cole; David Collier; Eve L Coomber; Nick Craddock; Mark J Daly; John Danesh; Marta DiForti; Alison Foster; Nelson B Freimer; Daniel Geschwind; Mandy Johnstone; Shelagh Joss; Georg Kirov; Jarmo Körkkö; Outi Kuismin; Peter Holmans; Christina M Hultman; Conrad Iyegbe; Jouko Lönnqvist; Minna Männikkö; Steve A McCarroll; Peter McGuffin; Andrew M McIntosh; Andrew McQuillin; Jukka S Moilanen; Carmel Moore; Robin M Murray; Ruth Newbury-Ecob; Willem Ouwehand; Tiina Paunio; Elena Prigmore; Elliott Rees; David Roberts; Jennifer Sambrook; Pamela Sklar; David St Clair; Juha Veijola; James T R Walters; Hywel Williams; Patrick F Sullivan; Matthew E Hurles; Michael C O'Donovan; Aarno Palotie; Michael J Owen; Jeffrey C Barrett
Journal:  Nat Neurosci       Date:  2016-03-14       Impact factor: 24.884

10.  De novo mutations in schizophrenia implicate synaptic networks.

Authors:  Menachem Fromer; Andrew J Pocklington; David H Kavanagh; Hywel J Williams; Sarah Dwyer; Padhraig Gormley; Lyudmila Georgieva; Elliott Rees; Priit Palta; Douglas M Ruderfer; Noa Carrera; Isla Humphreys; Jessica S Johnson; Panos Roussos; Douglas D Barker; Eric Banks; Vihra Milanova; Seth G Grant; Eilis Hannon; Samuel A Rose; Kimberly Chambert; Milind Mahajan; Edward M Scolnick; Jennifer L Moran; George Kirov; Aarno Palotie; Steven A McCarroll; Peter Holmans; Pamela Sklar; Michael J Owen; Shaun M Purcell; Michael C O'Donovan
Journal:  Nature       Date:  2014-01-22       Impact factor: 49.962

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  4 in total

Review 1.  Genetic-epigenetic interactions in cis: a major focus in the post-GWAS era.

Authors:  Catherine Do; Alyssa Shearer; Masako Suzuki; Mary Beth Terry; Joel Gelernter; John M Greally; Benjamin Tycko
Journal:  Genome Biol       Date:  2017-06-19       Impact factor: 13.583

2.  Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.

Authors:  Yanjie Yu; Yingni Lin; Yuto Takasaki; Chenyao Wang; Hiroki Kimura; Jingrui Xing; Kanako Ishizuka; Miho Toyama; Itaru Kushima; Daisuke Mori; Yuko Arioka; Yota Uno; Tomoko Shiino; Yukako Nakamura; Takashi Okada; Mako Morikawa; Masashi Ikeda; Nakao Iwata; Yuko Okahisa; Manabu Takaki; Shinji Sakamoto; Toshiyuki Someya; Jun Egawa; Masahide Usami; Masaki Kodaira; Akira Yoshimi; Tomoko Oya-Ito; Branko Aleksic; Kinji Ohno; Norio Ozaki
Journal:  Transl Psychiatry       Date:  2018-01-10       Impact factor: 6.222

3.  Accelerating Translational Research through Open Science: The Neuro Experiment.

Authors:  E Richard Gold
Journal:  PLoS Biol       Date:  2016-12-07       Impact factor: 8.029

4.  Genomic trade-offs: are autism and schizophrenia the steep price of the human brain?

Authors:  J M Sikela; V B Searles Quick
Journal:  Hum Genet       Date:  2018-01-15       Impact factor: 4.132

  4 in total

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