Benjamin M Neale (Benjamin Neale, Ben Neale, Benjamine Neale)

ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 119

Top Venues

Nature genetics

Nature

medRxiv : the preprint server for health sciences

Nature communications

Massachusetts General Hospital

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Massachusetts General Hospital May 20o 2018

United States

Associate Professor :: Analytic and Translational Genetics Unit

Publications

Rahul Gupta, Masahiro Kanai, Timothy J Durham, Kristin Tsuo, Jason G McCoy, Patrick F Chinnery, Konrad J Karczewski, Sarah E Calvo, Benjamin M Neale, Vamsi K Mootha
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. medRxiv : the preprint server for health sciences (2023)
Kai Yuan, Ryan J Longchamps, Antonio F Pardiñas, Mingrui Yu, Tzu-Ting Chen, Shu-Chin Lin, Yu Chen, Max Lam, Ruize Liu, Yan Xia, Zhenglin Guo, Wenzhao Shi, Chengguo Shen, null null, Mark J Daly, Benjamin M Neale, Yen-Chen A Feng, Yen-Feng Lin, Chia-Yen Chen, Michael O'Donovan, Tian Ge, Hailiang Huang
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. medRxiv : the preprint server for health sciences (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature 614 (7948) (2023)
Kai Yuan, Ryan J Longchamps, Antonio F Pardiñas, Mingrui Yu, Tzu-Ting Chen, Shu-Chin Lin, Yu Chen, Max Lam, Ruize Liu, Yan Xia, Zhenglin Guo, Wenzhao Shi, Chengguo Shen, null null, Mark J Daly, Benjamin M Neale, Yen-Chen A Feng, Yen-Feng Lin, Chia-Yen Chen, Michael O'Donovan, Tian Ge, Hailiang Huang
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. medRxiv : the preprint server for health sciences (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Kai Yuan, Ryan J Longchamps, Antonio F Pardiñas, Mingrui Yu, Tzu-Ting Chen, Shu-Chin Lin, Yu Chen, Max Lam, Ruize Liu, Yan Xia, Zhenglin Guo, Wenzhao Shi, Chengguo Shen, null null, Mark J Daly, Benjamin M Neale, Yen-Chen A Feng, Yen-Feng Lin, Chia-Yen Chen, Michael O'Donovan, Tian Ge, Hailiang Huang
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. medRxiv : the preprint server for health sciences (2023)
null null, Siwei Chen, Benjamin M Neale, Samuel Frank Berkovic
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences (2023)
Elizabeth G Atkinson, Mykyta Artomov, Alexander A Loboda, Heidi L Rehm, Daniel G MacArthur, Konrad J Karczewski, Benjamin M Neale, Mark J Daly
Discordant calls across genotype discovery approaches elucidate variants with systematic errors. Genome research (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics (2023)
null null, Siwei Chen, Benjamin M Neale, Samuel Frank Berkovic
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences (2023)
Clara Albiñana, Zhihong Zhu, Andrew J Schork, Andrés Ingason, Hugues Aschard, Isabell Brikell, Cynthia M Bulik, Liselotte V Petersen, Esben Agerbo, Jakob Grove, Merete Nordentoft, David Michael Hougaard, Thomas M Werge, Anders Dupont Børglum, Preben Bo Mortensen, John G McGrath, Benjamin M Neale, Florian Privé, Bjarni Johann Vilhjalmsson
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores. Nature communications 14 (1) (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature (2023)
Frederik H Lassen, Samvida S Venkatesh, Nikolas Baya, Wei Zhou, Alex Bloemendal, Benjamin M Neale, Benedikt Mathias Kessler, Nicola Whiffin, Cecilia M Lindgren, Duncan S Palmer
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. medRxiv : the preprint server for health sciences (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics 55 (2) (2023)
Ran Cui, Roy A Elzur, Masahiro Kanai, Jacob C Ulirsch, Omer Weissbrod, Mark J Daly, Benjamin M Neale, Zhou Fan, Hilary K Finucane
Improving fine-mapping by modeling infinitesimal effects. Nature genetics (2023)
Duncan S Palmer, Wei Zhou, Liam Abbott, Emilie M Wigdor, Nikolas Baya, Claire Churchhouse, Cotton Seed, Tim Poterba, Daniel King, Masahiro Kanai, Alex Bloemendal, Benjamin M Neale
Analysis of genetic dominance in the UK Biobank. Science (New York, N.Y.) 379 (6639) (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Pouria Salehi Nowbandegani, Anthony Wilder Wohns, Jenna L Ballard, Eric S Lander, Alex Bloemendal, Benjamin M Neale, Luke O' Connor
Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies. Nature genetics (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature (2023)
Gianmarco Mignogna, Caitlin E Carey, Robbee Wedow, Nikolas Baya, Mattia Cordioli, Nicola Pirastu, Rino Bellocco, Kathryn Fiuza Malerbi, Michel G Nivard, Benjamin M Neale, Raymond K Walters, Andrea Ganna
Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci. Nature human behaviour (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics 55 (2) (2023)
Rahul Gupta, Masahiro Kanai, Timothy J Durham, Kristin Tsuo, Jason G McCoy, Patrick F Chinnery, Konrad J Karczewski, Sarah E Calvo, Benjamin M Neale, Vamsi K Mootha
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. medRxiv : the preprint server for health sciences (2023)
Duncan S Palmer, Wei Zhou, Liam Abbott, Emilie M Wigdor, Nikolas Baya, Claire Churchhouse, Cotton Seed, Tim Poterba, Daniel King, Masahiro Kanai, Alex Bloemendal, Benjamin M Neale
Analysis of genetic dominance in the UK Biobank. Science (New York, N.Y.) 379 (6639) (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature (2023)
Michael H Guo, Laurent C Francioli, Sarah L Stenton, Julia K Goodrich, Nicholas A Watts, Moriel H Singer-Berk, Emily Groopman, Philip W Darnowsky, Matthew Solomonson, Samantha Baxter, null null, Grace Tiao, Benjamin M Neale, Joel N Hirschhorn, Heidi L Rehm, Mark J Daly, Anne H O'Donnell-Luria, Konrad J Karczewski, Daniel G MacArthur, Kaitlin E Samocha
Inferring compound heterozygosity from large-scale exome sequencing data. bioRxiv : the preprint server for biology (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature (2023)
Siwei Chen, Laurent C Francioli, Julia K Goodrich, Ryan L Collins, Masahiro Kanai, Qingbo S Wang, Jessica Alfoldi, Nicholas A Watts, Christopher Vittal, Laura D Gauthier, Timothy Poterba, Michael W Wilson, Yekaterina Tarasova, William Phu, Riley Grant, Mary T Yohannes, Zan Koenig, Yossi Farjoun, Eric Banks, Stacey Donnelly, Stacey Gabriel, Namrata Gupta, Steven Ferriera, Charlotte Tolonen, Sam Novod, Louis Bergelson, David Roazen, Valentin Ruano-Rubio, Miguel Covarrubias, Christopher Llanwarne, Nikelle Petrillo, Gordon Wade, Thibault Jeandet, Ruchi Munshi, Kathleen Tibbetts, null null, Anne H O'Donnell-Luria, Matthew Solomonson, Cotton Seed, Alicia R Martin, Michael E Talkowski, Heidi L Rehm, Mark J Daly, Grace Tiao, Benjamin M Neale, Daniel G MacArthur, Konrad J Karczewski
A genomic mutational constraint map using variation in 76,156 human genomes. Nature (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics 55 (2) (2023)
Rahul Gupta, Masahiro Kanai, Timothy J Durham, Kristin Tsuo, Jason G McCoy, Anna V Kotrys, Wei Zhou, Patrick F Chinnery, Konrad J Karczewski, Sarah E Calvo, Benjamin M Neale, Vamsi K Mootha
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Nature (2023)
Rahul Gupta, Masahiro Kanai, Timothy J Durham, Kristin Tsuo, Jason G McCoy, Patrick F Chinnery, Konrad J Karczewski, Sarah E Calvo, Benjamin M Neale, Vamsi K Mootha
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. medRxiv : the preprint server for health sciences (2023)
Satoshi Koyama, Ying Wang, Kaavya Paruchuri, M D Mesbah Uddin, So Mi Jemma Cho, Sarah M Urbut, Sara Haidermota, Whitney E Hornsby, Robert C Green, Mark J Daly, Benjamin M Neale, Patrick T Ellinor, Jordan W Smoller, Matthew S Lebo, Elizabeth W Karlson, Alicia R Martin, Pradeep Natarajan
Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. medRxiv : the preprint server for health sciences (2023)
null null, Siwei Chen, Benjamin M Neale, Samuel Frank Berkovic
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences (2023)
Kai Yuan, Ryan J Longchamps, Antonio F Pardiñas, Mingrui Yu, Tzu-Ting Chen, Shu-Chin Lin, Yu Chen, Max Lam, Ruize Liu, Yan Xia, Zhenglin Guo, Wenzhao Shi, Chengguo Shen, null null, Mark J Daly, Benjamin M Neale, Yen-Chen A Feng, Yen-Feng Lin, Chia-Yen Chen, Michael O'Donovan, Tian Ge, Hailiang Huang
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. medRxiv : the preprint server for health sciences (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature 614 (7948) (2023)
Rahul Gupta, Masahiro Kanai, Timothy J Durham, Kristin Tsuo, Jason G McCoy, Patrick F Chinnery, Konrad J Karczewski, Sarah E Calvo, Benjamin M Neale, Vamsi K Mootha
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. medRxiv : the preprint server for health sciences (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature 614 (7948) (2023)
Wenhan Lu, Laura D Gauthier, Timothy Poterba, Edoardo Giacopuzzi, Julia K Goodrich, Christine R Stevens, Daniel King, Mark J Daly, Benjamin M Neale, Konrad J Karczewski
CHARR efficiently estimates contamination from DNA sequencing data. bioRxiv : the preprint server for biology (2023)
Rahul Gupta, Masahiro Kanai, Timothy J Durham, Kristin Tsuo, Jason G McCoy, Patrick F Chinnery, Konrad J Karczewski, Sarah E Calvo, Benjamin M Neale, Vamsi K Mootha
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. medRxiv : the preprint server for health sciences (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature 614 (7948) (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics (2023)
Ditte Demontis, G Bragi Walters, Georgios Athanasiadis, Raymond K Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas Damm Als, Jinjie Duan, F Kyle Satterstrom, Jonas Byberg-Grauholm, Marie Bækved-Hansen, Ólafur Ó Guðmundsson, Sigurður H Magnusson, Gisli Baldursson, Katrin Davidsdottir, Gyda S Haraldsdottir, Esben Agerbo, Gabriel E Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribases, Dorret I Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P Howrigan, Sarah E Medland, Tetyana Zayats, Veera Manikandan Rajagopal, null null, null null, Merete Nordentoft, Ole Mors, David Michael Hougaard, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Hreinn Stefansson, Panagiotis Roussos, Barbara Franke, Thomas M Werge, Benjamin M Neale, Kári Stefánsson, Anders Dupont Børglum
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. Nature genetics 55 (2) (2023)
Daniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, Kushal K Dey, Benjamin M Neale, Elise B Robinson, Konrad J Karczewski, Luke O' Connor
Polygenic architecture of rare coding variation across 394,783 exomes. Nature 614 (7948) (2023)
Michael H Guo, Laurent C Francioli, Sarah L Stenton, Julia K Goodrich, Nicholas A Watts, Moriel Singer-Berk, Emily Groopman, Philip W Darnowsky, Matthew Solomonson, Samantha Baxter, null null, Grace Tiao, Benjamin M Neale, Joel N Hirschhorn, Heidi L Rehm, Mark J Daly, Anne H O'Donnell-Luria, Konrad J Karczewski, Daniel G MacArthur, Kaitlin E Samocha
Inferring compound heterozygosity from large-scale exome sequencing data. Nature genetics (2023)
Manuel Mattheisen, Jakob Grove, Thomas Damm Als, Joanna Martin, Georgios Voloudakis, Sandra Meier, Ditte Demontis, Jaroslav Bendl, Raymond K Walters, Caitlin E Carey, Anders Rosengren, Nora I Strom, Mads Engel Hauberg, Biao Zeng, Gabriel E Hoffman, Wen Zhang, Jonas Byberg-Grauholm, Marie Bækvad-Hansen, Esben Agerbo, Bru Cormand, Merete Nordentoft, Thomas M Werge, Ole Mors, David Michael Hougaard, Joseph D Buxbaum, Stephen V Faraone, Barbara Franke, Søren Dalsgaard, Preben B Mortensen, Elise B Robinson, Panagiotis Roussos, Benjamin M Neale, Mark J Daly, Anders Dupont Børglum
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups. Nature genetics 54 (10) (2022)
Veera Manikandan Rajagopal, Jinjie Duan, Laura Vilar-Ribó, Jakob Grove, Tetyana Zayats, Josep-Antoni Ramos-Quiroga, F Kyle Satterstrom, María Soler Artigas, Jonas Byberg-Grauholm, Marie Bækvad-Hansen, Thomas Damm Als, Anders Rosengren, Mark J Daly, Benjamin M Neale, Merete Nordentoft, Thomas M Werge, Ole Mors, David Michael Hougaard, Preben B Mortensen, Marta Ribases, Anders Dupont Børglum, Ditte Demontis
Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder. Nature genetics 54 (8) (2022)
Wei Zhou, Wenjian Bi, Zhangchen Zhao, Kushal K Dey, Karthik A Jagadeesh, Konrad J Karczewski, Mark J Daly, Benjamin M Neale, Seunggeun Lee
SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests. Nature genetics 54 (10) (2022)
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Luke M Evans, Rasool Tahmasbi, Scott I Vrieze, Gonçalo R Abecasis, Sayantan Das, Steven Gazal, Douglas W Bjelland, Teresa R de Candia, null null, Michael E Goddard, Benjamin M Neale, Jian Yang, Peter M Visscher, Matthew C Keller
Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits. Nature genetics 50 (5) (2018)
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas Damm Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Byberg-Grauholm, Marie Bækvad-Hansen, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Ashley Dumont, Nicholas Eriksson, Michael Gandal, Jacqueline I Goldstein, Katrina L Grasby, Jakob Grove, Olafur O Gudmundsson, Christine Søholm Hansen, Mads Engel Hauberg, Mads V Hollegaard, Daniel P Howrigan, Hailiang Huang, Julian B Maller, Alicia R Martin, Nicholas G Martin, Jennifer Moran, Jonatan Pallesen, Duncan S Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise B Robinson, F Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G Bragi Walters, Hyejung Won, Margaret J Wright, null null, null null, null null, Ole Andreas Andreassen, Philip Asherson, Christie L Burton, Dorret I Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H Geschwind, Hakon Hakonarson, Jan Haavik, Henry R Kranzler, Jonna Kuntsi, Kate Langley, Klaus-Peter Lesch, Christel Middeldorp, Andreas Reif, Luis Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund J S Sonuga-Barke, Patrick F Sullivan, Anita Thapar, Joyce Y Tung, Irwin D Waldman, Sarah E Medland, Kári Stefánsson, Merete Nordentoft, David Michael Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J Daly, Stephen V Faraone, Anders Dupont Børglum, Benjamin M Neale
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature genetics 51 (1) (2018)

Benjamin M Neale.css-eqlu8i{font-size:small;padding-left:4px;} (Benjamin Neale, Ben Neale, Benjamine Neale)

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Benjamin M Neale (Benjamin Neale, Ben Neale, Benjamine Neale)