logo
科言猫学术研究的AI总结
language
手机端手机端
  • Phone Feature微信小程序
简体中文简体中文
notice消息通知
博客博客
arrow
B

Benjamin M. Neale

broad institute of mit and harvard
H指数:160
被引数:21.4万

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Contribution of copy number variants to schizophrenia in East Asian populations

东亚人群中拷贝数变异对精神分裂症的贡献

Nature Genetics
IF29
2026-09-110
OAAI
Yu Chen; Qidi Feng; Max Lam; Mingrui Yu; Yaoyao Sun; Cong Huai; Bimal Jana; Jack Fu; Calwing Liao; Robert Ye; Soyeon Kim; Justin D. Tubbs; Omar Shanta; Bhooma Thiruvahindrapuram; Yawen Jen; Guorui Zhao; Jess Wang; Juan Xu; Wenzhao Shi; Stephen W. Scherer; Feng Zhu; Chih-Min Liu; Zhenglin Guo; Daniel Howrigan; Mark Daly; Benjamin M. Neale; Akira Sawa; Jonathan Sebat; Michael E. Talkowski; Jinsong Tang; Xiancang Ma; Wei J. Chen; Shengying Qin; Weihua Yue; Tian Ge; Hailiang Huang
Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome

基因组分析暗示多囊卵巢综合征中的激素和代谢失调

Nature Genetics
IF29
2026-04-230
OAAI
Loes M. E. Moolhuijsen; Jia Zhu; Benjamin H. Mullin; Natàlia Pujol-Gualdo; Ky’Era V. Actkins; Jasmine A. Mack; Hridya Rao; Bhavi Trivedi; Katherine A. Kentistou; Yajie Zhao; David Westergaard; Jaakko S. Tyrmi; Gudmar Thorleifsson; Yanfei Zhang; Laura Wittemans; Amber DeVries; Kelly Brewer; Ryan Sisk; Rebecca Danning; Michael H. Preuss; Michelle R. Jones; Katherine S. Ruth; Marianne Andersen; Ricardo Azziz; Karina Banasik; Michael Boehnke; Linda Broer; Søren Brunak; Yee-Ming Chan; Daniel I. Chasman; Mark Daly; David A. Ehrmann; Bart C. Fauser; Lars G. Fritsche; M. Geoffrey Hayes; Chunyan He; Hongyan Huang; Irina Kowalska; Peter Kraft; Richard S. Legro; Nan Lin; Ruth J. Loos; Yvonne V. Louwers; Reedik Magi; Mark I. McCarthy; Laure Morin-Papunen; Jean V. Morrison; Cynthia Morton; Girish N. Nadkarni; Benjamin M. Neale; Henriette Svarre Nielsen; Mette Nyegaard; Sisse R. Ostrowski; Ole B. V. Pedersen; Erik Sørensen; Christina Mikkelsen; Christian Erikstrup; Kathrine A. Kaspersen; Mie T. Bruun; Bitten Aagaard; Henrik Ullum; Barbara Obermayer-Pietsch; Aarno Palotie; Mary P. Reeve; Andres Salumets; Richa Saxena; Timothy D. Spector; Bronwyn G. A. Stuckey; Unnur Thorsteinsdottir; André G. Uitterlinden; Margrit Urbanek; Sebastian Zöllner; David A. van Heel; Joel N. Hirschhorn; Kari Stefansson; John R. B. Perry; Unnur Styrkarsdottir; Scott G. Wilson; Terhi Piltonen; Triin Laisk; Marjo-Riitta Jarvelin; Kharis Burns; Anne E. Justice; Hannele Laivuori; Ken K. Ong; Mark O. Goodarzi; Lea K. Davis; Andrea Dunaif; Cecilia M. Lindgren; Joop S. E. Laven; Stephen Franks; Jenny A. Visser; Corrine K. Welt; Tugce Karaderi; Felix R. Day
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多祖先全基因组分析确定与甲状腺癌和良性甲状腺疾病相关的基因和生物学途径

Nature Genetics
IF29
2026-02-050
OAAI
Samantha L. White; Maizy S. Brasher; Jack Pattee; Wei Zhou; Sinéad Chapman; Yon Ho Jee; Caitlin C. Bell; Taylor L. Jamil; Martin Barrio; Christopher H. Arehart; Luke M. Evans; Jibril Hirbo; Nancy J. Cox; Peter Straub; Shinichi Namba; Emily Bertucci-Richter; Lindsay Guare; Ahmed Edris; Sam Morris; Ashley J. Mulford; Haoyu Zhang; Brian Fennessy; Martin D. Tobin; Jing Chen; Alexander T. Williams; Catherine John; David A. van Heel; Rohini Mathur; Sarah Finer; Marta R. Moksnes; Ben M. Brumpton; Bjørn Olav Åsvold; Raitis Peculis; Vita Rovite; Ilze Konrade; Ying Wang; Kristy Crooks; Sameer Chavan; Matthew J. Fisher; Nicholas Rafaels; Meng Lin; Jonathan A. Shortt; Alan R. Sanders; David C. Whiteman; Stuart MacGregor; Sarah E. Medland; Unnur Thorsteinsdóttir; Kári Stefánsson; Tugce Karaderi; Kathleen M. Egan; Therese Bocklage; Hilary C. McCrary; Gregory Riedlinger; Bodour Salhia; Craig Shriver; Minh D. Phan; Janice L. Farlow; Stephen Edge; Varinder Kaur; Michelle L. Churchman; Robert J. Rounbehler; Pamela L. Brock; Matthew D. Ringel; Milton Pividori; Rebecca Schweppe; Christopher D. Raeburn; Robin G. Walters; Zhengming Chen; Liming Li; Koichi Matsuda; Yukinori Okada; Sebastian Zöllner; Anurag Verma; Michael H. Preuss; Eimear Kenny; Audrey E. Hendricks; Lauren Fishbein; Peter Kraft; Mark J. Daly; Benjamin M. Neale; Alicia R. Martin; Joanne B. Cole; Bryan R. Haugen; Christopher R. Gignoux; Nikita Pozdeyev
Mapping the genetic landscape across 14 psychiatric disorders

绘制14种精神疾病的遗传图谱

Nature
IF48.5
2025-12-100
OA
Andrew D. Grotzinger; Josefin Werme; Wouter J. Peyrot; Oleksandr Frei; Christiaan de Leeuw; Lucy K. Bicks; Qiuyu Guo; Michael P. Margolis; Brandon J. Coombes; Anthony Batzler; Vanessa Pazdernik; Joanna M. Biernacka; Ole A. Andreassen; Verneri Anttila; Anders D. Børglum; Gerome Breen; Na Cai; Ditte Demontis; Howard J. Edenberg; Stephen V. Faraone; Barbara Franke; Michael J. Gandal; Joel Gelernter; Alexander S. Hatoum; John M. Hettema; Emma C. Johnson; Katherine G. Jonas; James A. Knowles; Karestan C. Koenen; Adam X. Maihofer; Travis T. Mallard; Manuel Mattheisen; Karen S. Mitchell; Benjamin M. Neale; Caroline M. Nievergelt; John I. Nurnberger; Kevin S. O’Connell; Roseann E. Peterson; Elise B. Robinson; Sandra S. Sanchez-Roige; Susan L. Santangelo; Jeremiah M. Scharf; Hreinn Stefansson; Kari Stefansson; Murray B. Stein; Nora I. Strom; Laura M. Thornton; Elliot M. Tucker-Drob; Brad Verhulst; Irwin D. Waldman; G. Bragi Walters; Naomi R. Wray; Dongmei Yu; Phil H. Lee; Kenneth S. Kendler; Jordan W. Smoller
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation

FAVOR 2.0：一个用于解释基因组变异的在线资源，该资源对变异的功能注释进行了再工程化

NUCLEIC ACIDS RESEARCH
IF13.1
2025-12-011
PRE
Zhou, Hufeng; Verma, Vineet; Li, Xihao; Li, Zilin; Shedd, Nicole; Li, Thomas Cheng; Yang, Haoyu; Zhang, Alvin; Borsari, Beatrice; Buyske, Steven; Gerstein, Mark; Matise, Tara; Zody, Michael C.; Neale, Benjamin; Weng, Zhiping; Sunyaev, Shamil R.; Lin, Xihong
Genetics and context for precision health in Greater Boston

精准健康在大波士顿地区的遗传学与背景

Nature Communications
IF15.7
2025-11-260
OAAI
Satoshi Koyama; Ying Wang; Kaavya Paruchuri; Md Mesbah Uddin; So Mi J. Cho; Sarah M. Urbut; Yang Sui; Akl C. Fahed; Himani Kamineni; Sara Haidermota; Whitney E. Hornsby; Robert C. Green; Mark J. Daly; Benjamin M. Neale; Patrick T. Ellinor; Jordan W. Smoller; Susan A. Slaugenhaupt; Matthew S. Lebo; Elizabeth W. Karlson; Alicia R. Martin; Pradeep Natarajan
Rare genetic variants confer a high risk of ADHD and implicate neuronal biology

稀有遗传变异会增加ADHD的风险，并涉及神经元生物学。

Nature
IF48.5
2025-11-120
OAAI
Ditte Demontis; Jinjie Duan; Yu-Han H. Hsu; Greta Pintacuda; Jakob Grove; Trine Tollerup Nielsen; Janne Thirstrup; Makayla Martorana; Travis Botts; F. Kyle Satterstrom; Jonas Bybjerg-Grauholm; Jason H. Y. Tsai; Simon Glerup; Martine Hoogman; Jan Buitelaar; Marieke Klein; Georg C. Ziegler; Christian Jacob; Oliver Grimm; Maximilian Bayas; Nene F. Kobayashi; Sarah Kittel-Schneider; Klaus-Peter Lesch; Barbara Franke; Andreas Reif; Esben Agerbo; Thomas Werge; Merete Nordentoft; Ole Mors; Preben Bo Mortensen; Kasper Lage; Mark J. Daly; Benjamin M. Neale; Anders D. Børglum
Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effects

全英生物银行全基因组关联分析增强了祖先富集效应的发现和解析

Nature Genetics
IF0
2025-09-180
PRE
Konrad J. Karczewski; Rahul Gupta; Masahiro Kanai; Wenhan Lu; Kristin Tsuo; Ying Wang; Raymond K. Walters; Patrick Turley; Shawneequa Callier; Nirav N. Shah; Nikolas Baya; Duncan S. Palmer; Jacqueline I. Goldstein; Gopal Sarma; Matthew Solomonson; Nathan Cheng; Sam Bryant; Claire Churchhouse; Caroline M. Cusick; Timothy Poterba; John Compitello; Daniel King; Wei Zhou; Cotton Seed; Hilary K. Finucane; Mark J. Daly; Benjamin M. Neale; Elizabeth G. Atkinson; Alicia R. Martin
Multipopulation GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish

多人群静脉血栓栓塞症的全基因组关联研究鉴定了新的位点，随后在斑马鱼中进行实验验证

Blood Advances
IF7.1
2025-06-260
OAAI
Brooke N. Wolford; Queena Yakun Zhao; Kuan-Han H. Wu; Xinge Yu; Catherine E. Richter; Laxmi Bhatta; Ben M. Brumpton; Karl C. Desch; Florian Thibord; Derek Klarin; Andrew D. Johnson; David-Alexandre Trégouët; Scott M. Damrauer; Nicholas L. Smith; Valeria Lo Faro; Kristin Tsuo; Mark J. Daly; Benjamin M. Neale; Wei Zhou; Cristen J. Willer; Jordan A. Shavit; Ida Surakka
IDENTIFICATION OF HUB GENES INVOLVED IN EARLY-ONSET SCHIZOPHRENIA USING GENETICALLY PREDICTED REGULATED GENE-EXPRESSION RISK SCORE FOR SCHIZOPHRENIA

使用遗传预测的精神分裂症调节基因表达风险评分鉴定早发性精神分裂症中涉及的枢纽基因

EUROPEAN NEUROPSYCHOPHARMACOLOGY
IF6.7
2024-10-010
PRE
Jen, Yawen; Yu, Sung-Liang; Hsiao, Po-Chang; Liu, Chih-Min; Liu, Chen-Chung; Hwang, Tzung-Jeng; Hsieh, Ming H.; Huang, Hailiang; Chandler, Sharon D.; Faraone, Stephen; Neale, Benjamin; McCarroll, Steve; Tsuang, Ming T.; Hwu, Hai-Gwo; Chen, Wei J.

研究方向

暂未获取到该数据
M
Mark J. Daly
H 指数:224论文数:1,263被引数:40.9万
A
Anders D. Børglum
H 指数:101论文数:705被引数:5.9万
R
Raymond K. Walters
H 指数:49论文数:132被引数:3.8万
T
Thomas Werge
H 指数:104论文数:766被引数:6.3万
S
Stephen V. Faraone
H 指数:197论文数:1,856被引数:16.8万
S
Stephan Ripke
H 指数:126论文数:532被引数:12.5万
D
Ditte Demontis
H 指数:58论文数:281被引数:4.7万
J
Jordan W. Smoller
H 指数:130论文数:889被引数:9.9万
A
Alicia R. Martin
H 指数:62论文数:224被引数:5.4万
B
Barbara Franke
H 指数:118论文数:979被引数:6.6万