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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

Lea K. Davis Dongomei Yu; Clare L Keenan; Eric R Gamazon; Anuar I Konkashbaev; Eske M Derks; Benjamin M Neale; Jian Yang; S. Hong Lee; Patrick Evans; Cathy L Barr; Laura Bellodi; Fortu Benarroch; Gabriel Bedova Berrio; Oscar J Bienvenu; Michael H Bloch; Rianne M Blom; Ruth D Bruun; Cathy L Budman; Beatriz Camarena; Desmond Campbell; Carolina Cappi; Julio C. Cardona Salgado; Danielle C Cath; Maria C Cavallini; Denise A Chavira; Sylvain Chouinard; David V Conti; Edwin H Cook; Vladimir Coric; Bernadette A Cullen; Dieter Deforce; Richard Delorne; Yves Dion; Christopher K Edlund; Karin Egberts; Peter Falkai; Thomas V Fernandez; Patience J Gallagher; Helena Garrido; Daniel Geller; Simon L Girard; Hans J Grabe; Marco A Grados; Benjamin D Greenberg; Varda Gross Tsur; Stephen Haddad; Gary A Heiman; Sian M. J Hemmings; Ana G Hounie; Cornelia Illmann; Joseph Jankovic; Michael A Jenike; Robert A King; Barbara Kremeyer; Roger Kurlan; Nuria Lanzagorta; Marion Leboyer; James F Leckman; Leonhard Lennerts; Chunyu Liu; Christine Lochner; Thomas L Lowe; Fabio Macciardi; James T McCracken; Lauren MacGrant; Sandra C. Mesa Restrepo; Rainald Moessner; Jubel Morgan; Heike Muller; Dennis L Murphy; Allan L Naarden; William Cornejo Ochoa; Roel A Ophoff; Lisa Osieck; Andrew J Pakstis; Michele T Pato; Carlos N Pato; John Piacentini; Christopher Pittenger; Yehuda Pollak; Scott L Rauch; Tobias J Renner; Victor I Reus; Mark A Riddle; Mary M Robertson; Roxana Romero; Maria C Rosàrio; David Rosenberg; Guy A Rouleau; Stephan Ruhrmann; Andres Ruiz Linares; Aline S Sampaio; Jack Samuels; Paul Sandor; Brooke Sheppard; Harvey S Singer; Jan H Smit; Dan J Stein; E Strengman; Jay A Tischfield; Ana V. Valencia Duarte; Homero Pinto Vallada Filho; Filip Van Nieuwerburgh; Jeremy Veenstra VanderWeele; Susanne Walitza; Ying Wang; Jens R Wendland; Herman G. M Westenberg; Yin Yao Shugart; Eurípedes Constantino Miguel; William McMahon; Michael Wagner; Humberto Nicolini; Danielle Posthuma; Gregory L Hanna; Peter Heutink; Damiaan Denys; Paul D Arnold; Ben A Oostra; Gerald Nestadt; Nelson B Freimer; David L Pauls; Naomi R Wray; S. Evelyn Stewart; Carol A Mathews; James A Knowles; Nancy J Cox; Jeremiah M Scharf

Plos genetics San Francisco v. 9, n. 10, p. e1003864, 2013

San Francisco 2013

Localização: FM - Fac. Medicina    (BCSEP 483 2013 )(Acessar)

2
Clinical use of current polygenic risk scores may exacerbate health disparities
Clinical use of current polygenic risk scores may exacerbate health disparities
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Clinical use of current polygenic risk scores may exacerbate health disparities

Martin, Alicia R ; Kanai, Masahiro ; Kamatani, Yoichiro ; Okada, Yukinori ; Neale, Benjamin M ; Daly, Mark J

Nature genetics, 2019-04, Vol.51 (4), p.584-591 [Periódico revisado por pares]

United States: Nature Publishing Group

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3
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
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Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations

Martin, Alicia R. ; Gignoux, Christopher R. ; Walters, Raymond K. ; Wojcik, Genevieve L. ; Neale, Benjamin M. ; Gravel, Simon ; Daly, Mark J. ; Bustamante, Carlos D. ; Kenny, Eimear E.

American journal of human genetics, 2017-04, Vol.100 (4), p.635-649 [Periódico revisado por pares]

United States: Elsevier Inc

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4
Multi-trait analysis of genome-wide association summary statistics using MTAG
Multi-trait analysis of genome-wide association summary statistics using MTAG
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Multi-trait analysis of genome-wide association summary statistics using MTAG

Turley, Patrick ; Walters, Raymond K ; Maghzian, Omeed ; Okbay, Aysu ; Lee, James J ; Fontana, Mark Alan ; Nguyen-Viet, Tuan Anh ; Wedow, Robbee ; Zacher, Meghan ; Furlotte, Nicholas A ; Magnusson, Patrik ; Oskarsson, Sven ; Johannesson, Magnus ; Visscher, Peter M ; Laibson, David ; Cesarini, David ; Neale, Benjamin M ; Benjamin, Daniel J

Nature genetics, 2018-02, Vol.50 (2), p.229-237 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Predicting Polygenic Risk of Psychiatric Disorders
Predicting Polygenic Risk of Psychiatric Disorders
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Predicting Polygenic Risk of Psychiatric Disorders

Martin, Alicia R. ; Daly, Mark J. ; Robinson, Elise B. ; Hyman, Steven E. ; Neale, Benjamin M.

Biological psychiatry (1969), 2019-07, Vol.86 (2), p.97-109 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Phenome-wide heritability analysis of the UK Biobank
Phenome-wide heritability analysis of the UK Biobank
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Phenome-wide heritability analysis of the UK Biobank

Ge, Tian ; Chen, Chia-Yen ; Neale, Benjamin M ; Sabuncu, Mert R ; Smoller, Jordan W Domingue, Benjamin W.

PLoS genetics, 2017-04, Vol.13 (4), p.e1006711-e1006711 [Periódico revisado por pares]

United States: Public Library of Science

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7
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Gusev, Alexander ; Mancuso, Nicholas ; Won, Hyejung ; Kousi, Maria ; Finucane, Hilary K ; Reshef, Yakir ; Song, Lingyun ; Safi, Alexias ; McCarroll, Steven ; Neale, Benjamin M ; Ophoff, Roel A ; O'Donovan, Michael C ; Crawford, Gregory E ; Geschwind, Daniel H ; Katsanis, Nicholas ; Sullivan, Patrick F ; Pasaniuc, Bogdan ; Price, Alkes L

Nature genetics, 2018-04, Vol.50 (4), p.538-548 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Searching for missing heritability: Designing rare variant association studies
Searching for missing heritability: Designing rare variant association studies
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Searching for missing heritability: Designing rare variant association studies

Zuk, Or ; Schaffner, Stephen F ; Samocha, Kaitlin ; Do, Ron ; Hechter, Eliana ; Kathiresan, Sekar ; Daly, Mark J ; Neale, Benjamin M ; Sunyaev, Shamil R ; Lander, Eric S

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (4), p.E455-E464 [Periódico revisado por pares]

United States: National Academy of Sciences

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9
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
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Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

Genovese, Giulio ; Kähler, Anna K ; Handsaker, Robert E ; Lindberg, Johan ; Rose, Samuel A ; Bakhoum, Samuel F ; Chambert, Kimberly ; Mick, Eran ; Neale, Benjamin M ; Fromer, Menachem ; Purcell, Shaun M ; Svantesson, Oscar ; Landén, Mikael ; Höglund, Martin ; Lehmann, Sören ; Gabriel, Stacey B ; Moran, Jennifer L ; Lander, Eric S ; Sullivan, Patrick F ; Sklar, Pamela ; Grönberg, Henrik ; Hultman, Christina M ; McCarroll, Steven A

The New England journal of medicine, 2014-12, Vol.371 (26), p.2477-2487 [Periódico revisado por pares]

Waltham, MA: Massachusetts Medical Society

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10
Testing for an unusual distribution of rare variants
Testing for an unusual distribution of rare variants
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Testing for an unusual distribution of rare variants

Neale, Benjamin M ; Rivas, Manuel A ; Voight, Benjamin F ; Altshuler, David ; Devlin, Bernie ; Orho-Melander, Marju ; Kathiresan, Sekar ; Purcell, Shaun M ; Roeder, Kathryn ; Daly, Mark J Leal, Suzanne M.

PLoS genetics, 2011-03, Vol.7 (3), p.e1001322-e1001322 [Periódico revisado por pares]

United States: Public Library of Science

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Deste Autor:

  1. Knowles, J
  2. Yang, J
  3. Gallagher, P
  4. Fernandez, T
  5. Blom, R

Neste Assunto:

  1. Science & Technology
  2. Humans
  3. Life Sciences & Biomedicine
  4. Genetics & Heredity
  5. Genome-Wide Association Study

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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