Daniel P Howrigan (Daniel Howrigan)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 19

Top Topics

Dna Methylation

Autism Spectrum Disorder

Top Venues

Nature genetics

Nature human behaviour

bioRxiv : the preprint server for biology

Nature neuroscience

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

Publications

Caitlin E Carey, Rebecca Shafee, Robbee Wedow, Amanda Elliott, Duncan S Palmer, John Compitello, Masahiro Kanai, Liam Abbott, Patrick Schultz, Konrad J Karczewski, Samuel C Bryant, Caroline M Cusick, Claire Churchhouse, Daniel P Howrigan, Daniel King, George Davey Smith, Benjamin M Neale, Raymond K Walters, Elise B Robinson
Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation. Nature human behaviour 8 (8) (2024)
Caitlin E Carey, Rebecca Shafee, Robbee Wedow, Amanda Elliott, Duncan S Palmer, John Compitello, Masahiro Kanai, Liam Abbott, Patrick Schultz, Konrad J Karczewski, Samuel C Bryant, Caroline M Cusick, Claire Churchhouse, Daniel P Howrigan, Daniel King, George Davey Smith, Benjamin M Neale, Raymond K Walters, Elise B Robinson
Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation. Nature human behaviour 8 (8) (2024)
Toni A Boltz, Benjamin B Chu, Calwing Liao, Julia M Sealock, Robert Ye, Lerato Majara, Jack M Fu, Susan Service, Lingyu Zhan, Sarah E Medland, Sinéad B Chapman, Simone Rubinacci, Matthew DeFelice, Jonna L Grimsby, Tamrat Abebe, Melkam Alemayehu, Fred K Ashaba, Elizabeth G Atkinson, Tim B Bigdeli, Amanda B Bradway, Harrison Brand, Lori B Chibnik, Abebaw Fekadu, Michael Gatzen, Bizu Gelaye, Stella Gichuru, Marissa L Gildea, Toni C Hill, Hailiang Huang, Kalyn M Hubbard, Wilfred E Injera, Roxanne James, Moses Joloba, Christopher Kachulis, Phillip R Kalmbach, Kamulegeya Rogers, Gabriel Kigen, Soyeon Kim, Nastassja Koen, Edith Kamaru Kwobah, Joseph Kyebuzibwa, Seungmo Lee, Niall J Lennon, Penelope A Lind, Esteban A Lopera Maya, Johnstone Makale, Serghei Mangul, Justin McMahon, Pierre Mowlem, Henry Musinguzi, Rehema M Mwema, Noeline Nakasujja, Carter P Newman, Lethukuthula L Nkambule, Conor R O'Neil, Ana Maria Olivares, Catherine M Olsen, Linnet Ongeri, Sophie J Parsa, Adele Pretorius, Raj Ramesar, Faye L Reagan, Chiara Sabatti, Jacquelyn A Schneider, Welelta Shiferaw, Anne Stevenson, Erik Stricker, Rocky E Stroud, Jessie Tang, David C Whiteman, Mary T Yohannes, Mingrui Yu, Kai Yuan, null null, Dickens Akena, Lukoye Atwoli, Symon M Kariuki, Karestan C Koenen, Charles R J C Newton, Dan J Stein, Solomon Teferra, Zukiswa Zingela, Carlos N Pato, Michele T Pato, Carlos López-Jaramillo, Nelson Freimer, Roel A Ophoff, Loes M Olde Loohuis, Michael E Talkowski, Benjamin M Neale, Daniel P Howrigan, Alicia R Martin
A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner. bioRxiv : the preprint server for biology (2024)
Caitlin E Carey, Rebecca Shafee, Robbee Wedow, Amanda Elliott, Duncan S Palmer, John Compitello, Masahiro Kanai, Liam Abbott, Patrick Schultz, Konrad J Karczewski, Samuel C Bryant, Caroline M Cusick, Claire Churchhouse, Daniel P Howrigan, Daniel King, George Davey Smith, Benjamin M Neale, Raymond K Walters, Elise B Robinson
Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation. Nature human behaviour 8 (8) (2024)
Caitlin E Carey, Rebecca Shafee, Robbee Wedow, Amanda Elliott, Duncan S Palmer, John Compitello, Masahiro Kanai, Liam Abbott, Patrick Schultz, Konrad J Karczewski, Samuel C Bryant, Caroline M Cusick, Claire Churchhouse, Daniel P Howrigan, Daniel King, George Davey Smith, Benjamin M Neale, Raymond K Walters, Elise B Robinson
Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation. Nature human behaviour (2024)
Matthew DeFelice, Jonna L Grimsby, Daniel P Howrigan, Kai Yuan, Sinéad B Chapman, Christine R Stevens, Samuel DeLuca, Megan Townsend, Joseph D Buxbaum, Margaret Pericak-Vance, Shengying Qin, Dan J Stein, Solomon Teferra, Ramnik J Xavier, Hailiang Huang, Alicia R Martin, Benjamin M Neale
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays. bioRxiv : the preprint server for biology (2024)
Matthew DeFelice, Jonna L Grimsby, Daniel P Howrigan, Kai Yuan, Sinéad B Chapman, Christine R Stevens, Samuel DeLuca, Megan Townsend, Joseph D Buxbaum, Margaret Pericak-Vance, Shengying Qin, Dan J Stein, Solomon Teferra, Ramnik J Xavier, Hailiang Huang, Alicia R Martin, Benjamin M Neale
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays. bioRxiv : the preprint server for biology (2024)
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, Artigas María Soler, 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, Artigas María Soler, 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, Artigas María Soler, 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)
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, Artigas María Soler, 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)
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, Artigas María Soler, 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)
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, Artigas María Soler, 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, Artigas María Soler, 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)
Duncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, Rolf Adolfsson, Nick Bass, Douglas H R Blackwood, Marco P M Boks, Chia-Yen Chen, Claire Churchhouse, Aiden P Corvin, Nicholas Craddock, David Curtis, Arianna Di Florio, Faith Dickerson, Nelson A Freimer, Fernando S Goes, Xiaoming Jia, Ian R Jones, Lisa A Jones, Lina Jonsson, Rene S Kahn, Mikaél Landén, Adam E Locke, Andrew M McIntosh, Andrew McQuillin, Derek W Morris, Michael C O'Donovan, Roel A Ophoff, Michael J Owen, Nancy L Pedersen, Danielle Posthuma, Andreas Reif, Neil Risch, Catherine Schaefer, Laura J Scott, Tarjinder Singh, Jordan W Smoller, Matthew Solomonson, David St Clair, Eli A Stahl, Annabel Vreeker, James T R Walters, Weiqing Wang, Nicholas A Watts, Robert Yolken, Peter P Zandi, Benjamin M Neale
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. Nature genetics 54 (5) (2022)
Rahul Gupta, Konrad J Karczewski, Daniel P Howrigan, Benjamin M Neale, Vamsi K Mootha
Human genetic analyses of organelles highlight the nucleus in age-related trait heritability. eLife 10 (2021)
Daniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, Menachem Fromer, Felecia Cerrato, Wei J Chen, Claire Churchhouse, Kimberly Chambert, Sharon D Chandler, Mark J Daly, Ashley Dumont, Giulio Genovese, Hai-Gwo Hwu, Nan Laird, Jack A Kosmicki, Jennifer L Moran, Cheryl Roe, Tarjinder Singh, Shi-Heng Wang, Stephen V Faraone, Stephen J Glatt, Steven A McCarroll, Ming T Tsuang, Benjamin M Neale
Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. Nature neuroscience 23 (2) (2020)
Sali M K Farhan, Daniel P Howrigan, Liam E Abbott, Joseph R Klim, Simon D Topp, Andrea E Byrnes, Claire Churchhouse, Hemali Phatnani, Bradley N Smith, Evadnie Rampersaud, Gang Wu, Joanne Wuu, Aleksey Shatunov, Alfredo Iacoangeli, Ahmad Al Khleifat, Daniel A Mordes, Sulagna Ghosh, null null, null null, null null, null null, Kevin C Eggan, Rosa Rademakers, Hengameh Shams, Rebecca Schüle, Stephan Züchner, Michael Benatar, J Paul Taylor, Michael Nalls, Marc Gotkine, Pamela J Shaw, Karen E Morrison, Ammar Al Chalabi, Bryan Traynor, Christopher E Shaw, David B Goldstein, Matthew B Harms, Mark J Daly, Benjamin M Neale
Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature neuroscience 22 (12) (2019)
Jakob Grove, Stephan Ripke, Thomas Damm Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole Andreas Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D Buxbaum, Jonas Byberg-Grauholm, Marie Bækvad-Hansen, Felecia Cerrato, Kimberly Chambert, Jane Hvarregaard Christensen, Claire Churchhouse, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley L Dumont, Jacqueline I Goldstein, Christine Søholm Hansen, Mads Engel Hauberg, Mads V Hollegaard, Sigrun Hope, Daniel P Howrigan, Hailiang Huang, Christina M Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R Martin, Jennifer L Moran, Mette Nyegaard, Terje Nærland, Duncan S Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beate St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise B Robinson, Kathryn Roeder, Panos Roussos, Evald Saemundsen, Sven Sandin, F Kyle Satterstrom, George Davey Smith, Hreinn Stefansson, Stacy Steinberg, Christine R Stevens, Patrick F Sullivan, Patrick Turley, G Bragi Walters, Xinyi Xu, null null, null null, null null, null null, Kári Stefánsson, Daniel H Geschwind, Merete Nordentoft, David Michael Hougaard, Thomas M Werge, Ole Mors, Preben Bo Mortensen, Benjamin M Neale, Mark J Daly, Anders Dupont Børglum
Identification of common genetic risk variants for autism spectrum disorder. Nature genetics 51 (3) (2019)