Benjamin M. Neale

ScholarGPS® ID: 12768551963381

Affiliation
Massachusetts General Hospital, Boston, United States
Affiliation History

Field
Life Sciences
Discipline
Genetics
Top Specialties
Attention Deficit Hyperactivity Disorder | Human Genetics | Schizophrenia | Medical Genetics | Mutation | Translational Medicine | Biological Psychiatry | Meta-analysis | Autism | Autism Spectrum | Genetic Architecture | Spectrum Disorder | Exome Sequencing | Genomics | Molecular Genetics
Metrics Summary
Publication Count
250
Predicted Citations
73,420
Predicted h-index
88
Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

  • Publications
  • Books
  • Patents
  • NIH/NSF
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Improving fine-mapping by modeling infinitesimal effects (journal article)
Cui, Ran | Elzur, Roy A. | Kanai, Masahiro | Ulirsch, Jacob C. | Weissbrod, Omer | Daly, Mark J. | Neale, Benjamin M. | Fan, Zhou | Finucane, Hilary K.
Nature Genetics, volume 56, issue 1, pages 162-169 (2024).
10.1038/s41588-023-01597-3
Cite | Source
CHARR efficiently estimates contamination from DNA sequencing data (journal article)
Lu, Wenhan | Gauthier, Laura D. | Poterba, Timothy | Giacopuzzi, Edoardo | Goodrich, Julia K. | Stevens, Christine R. | King, Daniel | Daly, Mark J. | Neale, Benjamin M. | Karczewski, Konrad J.
The American Journal of Human Genetics, volume 110, issue 12, pages 2068-2076 (2023).
10.1016/j.ajhg.2023.10.011
Cited by (1) | Cite | Source
Bayesian multivariate genetic analysis improves translational insights (journal article)
Urbut, Sarah M. | Koyama, Satoshi | Hornsby, Whitney | Bhukar, Rohan | Kheterpal, Sumeet | Truong, Buu | Selvaraj, Margaret S. | Neale, Benjamin | O’Donnell, Christopher J. | Peloso, Gina M. | Natarajan, Pradeep
iScience, volume 26, issue 10, pages 107854- (2023).
10.1016/j.isci.2023.107854
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T83. CONTRIBUTION OF COMMON AND RARE VARIANTS TO SCHIZOPHRENIA RISK IN EAST AND SOUTH ASIAN ANCESTRIES (journal article)
Kim, Soyeon | Hassan, Arsalan | Huai, Cong | Guo, Zhenglin | Vincent, John | Mattheisen, Manuel | Neale, Benjamin | Ayub, Muhammad | Qin, Shengying | Knowles, James | Huang, Hailiang
European Neuropsychopharmacology, volume 75 (2023).
10.1016/j.euroneuro.2023.08.367
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T63. CROSS-DISORDER ANALYSIS OF AUTISM AND ADHD USING RARE VARIANTS: INSIGHTS FROM DANISH IPSYCH EXOMES (journal article)
Duan, Jinjie | Grove, Jakob | Demontis, Ditte | Satterstrom, F. Kyle | Fu, Jack | Carey, Caitlin | Sanders, Stephan J. | Devlin, Bernie | Roeder, Kathryn | Buxbaum, Joseph | ... | Børglum, Anders
European Neuropsychopharmacology, volume 75 (2023).
10.1016/j.euroneuro.2023.08.348
Cite | Source
84. SCHEMA 3.0: INCREASING GENETIC DIVERSITY AND GENE DISCOVERY FOR RARE-VARIANT ANALYSIS OF SCHIZOPHRENIA (journal article)
Sealock, Julia | Neale, Benjamin
European Neuropsychopharmacology, volume 75 (2023).
10.1016/j.euroneuro.2023.08.188
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2. BIPEX 2.0: LARGE-SCALE EXOME SEQUENCING OF OVER 75,000 INDIVIDUALS IDENTIFIES NOVEL GENETIC INSIGHTS INTO BIPOLAR DISORDER (journal article)
Liao, Calwing | Talkowski, Michael | Neale, Benjamin
European Neuropsychopharmacology, volume 75 (2023).
10.1016/j.euroneuro.2023.08.113
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ENHANCING POLYGENIC PREDICTION WITH AN AGNOSTIC MULTI-PGS METHOD THAT LEVERAGES HUNDREDS OF POLYGENIC SCORES (journal article)
Albiñana, Clara | Zhu, Zhihong | Schork, Andrew | Ingason, Andres | Aschard, Hugues | Brikell, Isabell | Petersen, Liselotte | Agerbo, Esben | Grove, Jakob | Børglum, Anders | ... | Vilhjalmsson, Bjarni
European Neuropsychopharmacology, volume 75 (2023).
10.1016/j.euroneuro.2023.08.065
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INSIGHTS FROM >80 LOCI ASSOCIATED WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER (journal article)
Walters, Raymond | Demontis, Ditte | Athanasiadis, Georgios | Walters, G. Bragi | Zayats, Tetyana | Howrigan, Daniel | Faraone, Stephen V. | Stefansson, Kari | Werge, Thomas | Børglum, Anders | ... | Franke, Barbara
European Neuropsychopharmacology, volume 75 (2023).
10.1016/j.euroneuro.2023.08.048
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Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies (journal article)
Salehi Nowbandegani, Pouria | Wohns, Anthony Wilder | Ballard, Jenna L. | Lander, Eric S. | Bloemendal, Alex | Neale, Benjamin M. | O’Connor, Luke J.
Nature Genetics, volume 55, issue 9, pages 1494-1502 (2023).
10.1038/s41588-023-01487-8
Cited by (5) | Cite | Source
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans (journal article)
Gupta, Rahul | Kanai, Masahiro | Durham, Timothy J. | Tsuo, Kristin | McCoy, Jason G. | Kotrys, Anna V. | Zhou, Wei | Chinnery, Patrick F. | Karczewski, Konrad J. | Calvo, Sarah E. | ... | Mootha, Vamsi K.
Nature, volume 620, issue 7975, pages 839-848 (2023).
10.1038/s41586-023-06426-5
Cited by (31) | Cite | Source
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores (journal article)
Albiñana, Clara | Zhu, Zhihong | Schork, Andrew J. | Ingason, Andrés | Aschard, Hugues | Brikell, Isabell | Bulik, Cynthia M. | Petersen, Liselotte V. | Agerbo, Esben | Grove, Jakob | ... | Vilhjálmsson, Bjarni J.
Nature Communications, volume 14, issue 1 (2023).
10.1038/s41467-023-40330-w
Cited by (7) | Cite | Source
Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci (journal article)
Mignogna, Gianmarco | Carey, Caitlin E. | Wedow, Robbee | Baya, Nikolas | Cordioli, Mattia | Pirastu, Nicola | Bellocco, Rino | Malerbi, Kathryn Fiuza | Nivard, Michel G. | Neale, Benjamin M. | ... | Ganna, Andrea
Nature Human Behaviour, volume 7, issue 8, pages 1371-1387 (2023).
10.1038/s41562-023-01632-7
Cited by (7) | Cite | Source
Discordant calls across genotype discovery approaches elucidate variants with systematic errors (journal article)
Atkinson, Elizabeth G. | Artomov, Mykyta | Loboda, Alexander A. | Rehm, Heidi L. | MacArthur, Daniel G. | Karczewski, Konrad J. | Neale, Benjamin M. | Daly, Mark J.
Genome Research, volume 33, issue 6, pages 999-1005 (2023).
10.1101/gr.277908.123
Cite | Source
Analysis of genetic dominance in the UK Biobank (journal article)
Palmer, Duncan S. | Zhou, Wei | Abbott, Liam | Wigdor, Emilie M. | Baya, Nikolas | Churchhouse, Claire | Seed, Cotton | Poterba, Tim | King, Daniel | Kanai, Masahiro | ... | Neale, Benjamin M.
Science, volume 379, issue 6639, pages 1341-1348 (2023).
10.1126/science.abn8455
Cited by (11) | Cite | Source
Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility (journal article)
Meyer, Michelle N. | Appelbaum, Paul S. | Benjamin, Daniel J. | Callier, Shawneequa L. | Comfort, Nathaniel | Conley, Dalton | Freese, Jeremy | Garrison, Nanibaa' A. | Hammonds, Evelynn M. | Harden, K. Paige | ... | Parens, Erik
Hastings Center Report, volume 53, issue S1 (2023).
10.1002/hast.1477
Cited by (15) | Cite | Source
Polygenic architecture of rare coding variation across 394,783 exomes (journal article)
Weiner, Daniel J. | Nadig, Ajay | Jagadeesh, Karthik A. | Dey, Kushal K. | Neale, Benjamin M. | Robinson, Elise B. | Karczewski, Konrad J. | O’Connor, Luke J.
Nature, volume 614, issue 7948, pages 492-499 (2023).
10.1038/s41586-022-05684-z
Cited by (52) | Cite | Source
Ancestry: How researchers use it and what they mean by it (journal article)
Dauda, Bege | Molina, Santiago J. | Allen, Danielle S. | Fuentes, Agustin | Ghosh, Nayanika | Mauro, Madelyn | Neale, Benjamin M. | Panofsky, Aaron | Sohail, Mashaal | Zhang, Sarah R. | Lewis, Anna C. F.
Frontiers in Genetics, volume 14 (2023).
10.3389/fgene.2023.1044555
Cited by (8) | Cite | Source
Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity (journal article)
Tsuo, Kristin | Zhou, Wei | Wang, Ying | Kanai, Masahiro | Namba, Shinichi | Gupta, Rahul | Majara, Lerato | Nkambule, Lethukuthula L. | Morisaki, Takayuki | Okada, Yukinori | ... | Martin, Alicia R.
Cell Genomics, volume 2, issue 12, pages 100212- (2022).
10.1016/j.xgen.2022.100212
Cited by (27) | Cite | Source
A scoping review of guidelines for the use of race, ethnicity, and ancestry reveals widespread consensus but also points of ongoing disagreement (journal article)
Mauro, Madelyn | Allen, Danielle S. | Dauda, Bege | Molina, Santiago J. | Neale, Benjamin M. | Lewis, Anna C.F.
The American Journal of Human Genetics, volume 109, issue 12, pages 2110-2125 (2022).
10.1016/j.ajhg.2022.11.001
Cited by (13) | Cite | Source