ScholarIQanswers from OpenAlex & ORCID
David M. Hougaard
ResearcherPublications, citations & collaboration network
David M. Hougaard is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does David M. Hougaard have?
ScholarIQindexed works
David M. Hougaard has 606 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does David M. Hougaard have?
ScholarIQcitation count
David M. Hougaard has 62,044 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of David M. Hougaard?
ScholarIQh-index
David M. Hougaard has an h-index of 99 in OpenAlex.
What is the i10-index of David M. Hougaard?
ScholarIQi10-index
David M. Hougaard has an i10-index of 382 in OpenAlex.
What is the ORCID of David M. Hougaard?
ScholarIQorcid
The ORCID for David M. Hougaard is on the source record.
What is the OpenAlex record for David M. Hougaard?
ScholarIQopenalex
The OpenAlex for David M. Hougaard is on the source record.
What are the most-cited papers on David M. Hougaard?
ScholarIQmost cited works
Identification of common genetic risk variants for autism spectrum disorder
Jakob Grove, BUPGEN, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Claire Churchhouse, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. 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, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum
Common variants conferring risk of schizophrenia
†Genetic Risk and Outcome in Psychosis (GROUP), Hreinn Stefánsson, Roel A. Ophoff, Stacy Steinberg, Ole A. Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli Pietiläinen, Ole Mors, Preben Bo Mortensen, Engilbert Sigurðsson, Ómar Gústafsson, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Folkmann Hansen, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Anders D. Børglum, Annette M. Hartmann, Anders Fink‐Jensen, Merete Nordentoft, David M. Hougaard, Bent Nørgaard‐Pedersen, Yvonne Böttcher, Jes Olesen, René Breuer, Hans‐Jürgen Möller, Ina Giegling, Henrik B. Rasmussen, Sally Timm, Manuel Mattheisen, István Bitter, János Réthelyi, Brynja B. Magnúsdóttir, Thordur Sigmundsson, Pall I. Olason, Gísli Másson, Jeffrey R. Gulcher, Magnús Haraldsson, Ragnheiður Fossdal, Thorgeir E. Thorgeirsson, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, Barbara Franke, Eric Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Julio Sanjuán, Rosa de Frutos, Elvira Bramon, Evangelos Vassos, Gillian Fraser, Ulrich Ettinger, Marco Picchioni, Nicholas Walker, Timi Toulopoulou, Anna C. Need, Dongliang Ge, Joeng Lim Yoon, Kevin V. Shianna, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Ãngel Carracedo, Celso Arango, Javier Costas, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Paul M. Matthews, Pierandrea Muglia, Leena Peltonen, David St Clair, David B. Goldstein, Kāri Stefánsson, David Collier
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
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 D. Als, Jinjie Duan, F. Kyle Satterstrom, Jonas Bybjerg‐Grauholm, Marie Bækved-Hansen, Ólafur Ó. Guðmundsson, Sigurður H. Magnússon, Gísli Baldursson, Katrín Davíðsdóttir, Gyða S. Haraldsdóttir, Esben Agerbo, Gabriel E. Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribasés, Dorret I. Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P. Howrigan, Sarah E. Medland, Tetyana Zayats, Veera M. Rajagopal, Alexandra Havdahl, Alysa E. Doyle, Andreas Reif, Anita Thapar, Bru Cormand, Calwing Liao, Christie L. Burton, Claiton H.D. Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Henrik Larsson, Ian R. Gizer, Irwin D. Waldman, Isabell Brikell, Jan Haavik, Jennifer Crosbie, James J. McGough, Jonna Kuntsi, Joseph Glessner, K. Langley, Klaus‐Peter Lesch, Luís Augusto Rohde, Mara Helena Hutz, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Michael O‘Donovan, Ole A. Andreassen, Patrick W. L. Leung, Pedro Mário Pan, Ridha Joober, Russell Schachar, Sandra K. Loo, Stephanie H. Witt, Ted Reichborn‐Kjennerud, Tobias Banaschewski, Ziarih Hawi, Mark J. Daly, Ole Mors, Merete Nordentoft, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Hreinn Stefánsson, Panos Roussos, Barbara Franke, Thomas Werge, Benjamin M. Neale, Kāri Stefánsson, Anders D. Børglum
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ãngel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations
Klaus Bønnelykke, Patrick Sleiman, Kasper Nielsen, Eskil Kreiner‐Møller, Josep M. Mercader, Danielle Belgrave, Herman T. den Dekker, Anders Husby, Astrid Sevelsted, Grissel Faura-Tellez, Li Juel Mortensen, Lavinia Paternoster, Richard Flaaten, Anne Mølgaard, David E. Smart, Philip Francis Thomsen, Morten Arendt Rasmussen, Sílvia Bonàs‐Guarch, Claus Holst, Ellen A. Nøhr, Rachita Yadav, Michael March, Thomas Blicher, Peter M. Lackie, Vincent W. V. Jaddoe, Angela Simpson, John W. Holloway, Liesbeth Duijts, Adnan Čustović, Donna E. Davies, David Torrents, Ramneek Gupta, Mads V. Hollegaard, David M. Hougaard, Håkon Håkonarson, Hans Bisgaard