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Petr Danecek

ResearcherPublications, citations & collaboration network

Petr Danecek is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Petr Danecek have?

ScholarIQindexed works

Petr Danecek has 97 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Petr Danecek have?

ScholarIQcitation count

Petr Danecek has 97,458 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Petr Danecek?

ScholarIQh-index

Petr Danecek has an h-index of 46 in OpenAlex.

What is the i10-index of Petr Danecek?

ScholarIQi10-index

Petr Danecek has an i10-index of 63 in OpenAlex.

What is the ORCID of Petr Danecek?

ScholarIQorcid

The ORCID for Petr Danecek is on the source record.

What is the OpenAlex record for Petr Danecek?

ScholarIQopenalex

The OpenAlex for Petr Danecek is on the source record.

What are the most-cited papers on Petr Danecek?

ScholarIQmost cited works
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy, Yang Luo, Arthur Gilly, Jeffrey C. Barrett, Eleftheria Zeggini, Nicole Soranzo, Klaudia Walter, Carl A. Anderson, Richard Durbin, Sayantan Das, Hyun Min Kang, Christian Fuchsberger, Alan Kwong, Laura J. Scott, Sai Chen, Michael Boehnke, Abecasis Gb, Warren Kretzschmar, Anubha Mahajan, Mark I McCarthy, Jonathan Marchini, Olivier Delaneau, Andrew R Wood, Marcus A. Tuke, Timothy Frayling, Alexander Teumer, Matthias Nauck, Petr Danecek, Kevin Sharp, Carlo Sidore, Andrea Angius, Fabio Busonero, Francesco Cucca, Nicholas J. Timpson, Laura J. Corbin, George Davey Smith, Josine L. Min, Seppo Koskinen, V Salomaa, Scott Vrieze, He Zhang, Cristen J. Willer, Jan H. Veldink, Leonard H. van den Berg, Wouter van Rheenen, Annelot M. Dekker, Ulrike Peters, Tabitha A. Harrison, Charles Kooperberg, Carlos N. Pato, Michele T. Pato, Cornelia M. van Duijn, Christopher E. Gillies, Matthew G. Sampson, Ilaria Gandin, Massimiliano Cocca, Nicola Pirastu, Paolo Gasparini, Massimo Mezzavilla, Michela Traglia, Cinzia Sala, Daniela Toniolo, Dorrett Boomsma, Kari Branham, Gerome Breen, Chad M. Brummett, Ross M. Fraser, Harry Campbell, James F. Wilson, Andrew T. Chan, Matthias Kretzler, Emily Y. Chew, Francis S. Collins, George Dedoussis, Aliki‐Eleni Farmaki, Marcus Dörr, Uwe Völker, Luigi Ferrucci, Lukas Forer, Sebastian Schoenherr, Stacey Gabriel, Palotie A, David Altshuler, Shawn Levy, R Myers, Leif Groop, Andrew Hattersley, Oddgeir L. Holmen, Kristian Hveem, James Lee, M McGue, William Iacono, Thomas Meitinger, David Melzer, Karen L Mohlke, John B Vincent, Deborah Nickerson, Melvin McInnis, J Brent Richards, Kerrin Small
Nature Genetics. 20163,312 CitationsOPEN ACCESS
The UK10K project identifies rare variants in health and disease
Writing group, Klaudia Walter, Josine L. Min, Jie Huang, Lucy Crooks, Yasin Memari, Shane McCarthy, John R. B. Perry, Changjiang Xu, Marta Futema, Daniel Lawson, Valentina Iotchkova, Stephan Schiffels, Audrey E. Hendricks, Petr Danecek, Rui Li, James S. Floyd, Louise V. Wain, Inês Barroso, Steve E. Humphries, Matthew E. Hurles, Eleftheria Zeggini, Jeffrey C. Barrett, Vincent Plagnol, J. Brent Richards, Celia M. T. Greenwood, Nicholas J. Timpson, Richard Durbin, Nicole Soranzo, Production group, Senduran Bala, Peter Clapham, Guy Coates, Tony Cox, Allan Daly, Petr Danecek, Yuanping Du, Richard Durbin, Sarah Edkins, Peter Ellis, Paul Flicek, Xiaosen Guo, Xueqin Guo, Liren Huang, David K. Jackson, Christopher Joyce, Thomas Keane, Anja Kolb-Kokocinski, Cordelia Langford, Rui Li, Jieqin Liang, Hong Lin, Ryan Liu, John Maslen, Shane McCarthy, Dawn Muddyman, Michael A. Quail, Jim Stalker, Jianping Sun, Jing Tian, Guangbiao Wang, Jun Wang, Yu Wang, Kim Wong, Pingbo Zhang, Cohorts group, Inês Barroso, Ewan Birney, Chris Boustred, Lu Chen, Gail Clement, Massimiliano Cocca, Petr Danecek, George Davey Smith, Ian N.M. Day, Aaron Day-Williams, Thomas A. Down, Ian Dunham, Richard Durbin, David M. Evans, Tom R. Gaunt, Matthias Geihs, Celia M. T. Greenwood, Deborah Hart, Audrey E. Hendricks, Bryan Howie, Jie Huang, Tim Hubbard, Pirro G. Hysi, Valentina Iotchkova, Yalda Jamshidi, Konrad J. Karczewski, John P. Kemp, Geneviève Lachance, Daniel Lawson, Monkol Lek, Margarida Lopes, Daniel G. MacArthur, Jonathan Marchini, Massimo Mangino
Nature. 20151,194 CitationsOPEN ACCESS
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Joanna Kaplanis, Kaitlin E. Samocha, Laurens Wiel, Zhancheng Zhang, Kevin J. Arvai, Ruth Y. Eberhardt, Giuseppe Gallone, Stefan H. Lelieveld, Hilary C. Martin, Jeremy F. McRae, Patrick Short, Rebecca I. Torene, Elke de Boer, Petr Danecek, Eugene J. Gardner, Ni Huang, Jenny Lord, Iñigo Martincorena, Rolph Pfundt, Margot R.F. Reijnders, Alison Yeung, Helger G. Yntema, Deciphering Developmental Disorders Study, Sílvia Borràs, Caroline Clark, John Dean, Zosia Miedzybrodzka, Alison Ross, Stephen Tennant, Tabib Dabir, Deirdre Donnelly, Mervyn Humphreys, Alex Magee, Vivienne McConnell, Shane McKee, Susan McNerlan, Patrick J. Morrison, Gillian Rea, Fiona Stewart, Trevor Cole, Nicola Cooper, Lisa Cooper‐Charles, Helen Cox, Lily Islam, Joanna Jarvis, Rebecca Keelagher, Derek Lim, Dominic McMullan, Jenny Morton, Swati Naik, Mary O’Driscoll, Kai‐Ren Ong, Deborah Osio, Nicola Ragge, Sarah Turton, Julie Vogt, Denise Williams, Simon Bodek, Alan Donaldson, Alison Hills, Karen Low, Ruth Newbury‐Ecob, Andrew Norman, Eileen Roberts, Ingrid Scurr, Sarah Smithson, Madeleine Tooley, Steve Abbs, Ruth Armstrong, Carolyn Dunn, Simon Holden, Soo‐Mi Park, Joan Paterson, Lucy Raymond, Evan Reid, Richard Sandford, Ingrid Simonic, Marc Tischkowitz, Geoff Woods, Lisa Bradley, Joanne Comerford, Andrew Green, Sally Ann Lynch, Shirley McQuaid, Brendan Mullaney, Jonathan Berg, David Goudie, Eleni Mavrak, Joanne McLean, Catherine McWilliam, Eleanor Reavey, Tara Azam, Elaine Cleary, Andrew P. Jackson, Wayne Lam, Anne Lampe, David Moore, Mary Porteous, Emma L. Baple, Júlia Baptista
Nature. 2020690 CitationsOPEN ACCESS
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Olivier Delaneau, Jonathan Marchini, Gil McVean, Peter Donnelly, Gerton Lunter, Jonathan Marchini, Simon Myers, Anjali Gupta Hinch, Zamin Iqbal, Iain Mathieson, Andy Rimmer, Dionysia K. Xifara, Angeliki Kerasidou, Claire Churchhouse, Olivier Delaneau, David Altshuler, Stacey Gabriel, Eric S. Lander, Namrata Gupta, Mark J. Daly, Mark A. DePristo, Eric Banks, Gaurav Bhatia, Mauricio O. Carneiro, Guillermo del Angel, Giulio Genovese, Robert E. Handsaker, Chris Hart, Steven A. McCarroll, James Nemesh, Ryan Poplin, S. F. Schaffner, Khalid Shakir, Pardis C. Sabeti, Sharon R. Grossman, Shervin Tabrizi, Ridhi Tariya, Heng Li, David Reich, Richard Durbin, Matthew E. Hurles, Senduran Balasubramaniam, John H. Burton, Petr Danecek, Thomas Keane, Anja Kolb-Kokocinski, Shane McCarthy, James Stalker, Michael A. Quail, Qasim Ayub, Yuan Chen, Alison J. Coffey, Vincenza Colonna, Ni Huang, Luke Jostins, Aylwyn Scally, Klaudia Walter, Yali Xue, Yujun Zhang, Ben Blackburne, Sarah Lindsay, Zemin Ning, Adam Frankish, Jennifer Harrow, Chris Tyler‐Smith, Gonalo R. Abecasis, Hyun Min Kang, Paul Anderson, Tom Blackwell, Fabio Busonero, Christian Fuchsberger, Goo Jun, Andrea Maschio, Eleonora Porcu, Carlo Sidore, Adrian Tan, Mary Kate Trost, David Bentley, Russell Grocock, Sean Humphray, Terena James, Zoya Kingsbury, Markus Bauer, R. Keira Cheetham, Tony Cox, Michael A. Eberle, Lisa Murray, Richard J. Shaw, Aravinda Chakravarti, Andrew G. Clark, Alon Keinan, Juan L. Rodríguez-Flores, Francisco M. De La Vega, Jeremiah D. Degenhardt, Evan E. Eichler, Paul Flicek, Laura Clarke, Rasko Leinonen, Richard E. Smith, Xiangqun Zheng-Bradley
Nature Communications. 2014460 CitationsOPEN ACCESS

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