Klaudia Walter

Active 2004–2025

51
Papers
34,091
Citations
38
h-index
49
i10-index

Citations

Citations per year for Klaudia Walter1928: 1 citations1985: 1 citations1992: 1 citations1993: 2 citations1994: 1 citations1996: 1 citations2000: 2 citations2002: 2 citations2003: 1 citations2004: 3 citations2005: 24 citations2006: 42 citations2007: 41 citations2008: 30 citations2009: 156 citations2010: 241 citations2011: 290 citations2012: 314 citations2013: 462 citations2014: 604 citations2015: 726 citations2016: 703 citations2017: 696 citations2018: 627 citations2019: 1,467 citations2020: 1,344 citations2021: 1,313 citations2022: 942 citations2023: 706 citations2024: 996 citations2025: 397 citations2026: 25 citations1929–1984: no citations, so these years are not shown1986–1991: no citations, so these years are not shown1995: no citations, so this year is not shown1997–1999: no citations, so these years are not shown2001: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 5,845 citing papers, 21.7% of this breakdownUnited Kingdom: 2,771 citing papers, 10.3% of this breakdownChina: 1,648 citing papers, 6.1% of this breakdownGermany: 1,542 citing papers, 5.7% of this breakdownNetherlands: 1,091 citing papers, 4.1% of this breakdownCanada: 1,061 citing papers, 4% of this breakdownAustralia: 979 citing papers, 3.6% of this breakdownFrance: 840 citing papers, 3.1% of this breakdownItaly: 808 citing papers, 3% of this breakdownSweden: 800 citing papers, 3% of this breakdownSpain: 720 citing papers, 2.7% of this breakdownDenmark: 597 citing papers, 2.2% of this breakdown
0%21.7%Other 30.5%

Fields

  • Biochemistry, Genetics and Molecular Biology66.2%
  • Medicine21.1%
  • Immunology and Microbiology2.8%
  • Agricultural and Biological Sciences2.5%
  • Neuroscience2.4%
  • Computer Science1.5%
  • Other3.5%

Topics

  • Genetic Associations and Epidemiology9%
  • Genomics and Phylogenetic Studies5.2%
  • Genomics and Rare Diseases5%
  • Genomic variations and chromosomal abnormalities3.9%
  • Genetic Mapping and Diversity in Plants and Animals2.3%
  • Cancer Genomics and Diagnostics2.3%
  • Other72.3%

Coauthors

All papers

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  1. A reference panel of 64,976 haplotypes for genotype imputation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrew R. Wood, Marcus A. Tuke, Timothy M. Frayling, Alexander Teumer, Matthias Nauck, Alexander Teumer, Petr Danecek, Kevin Sharp, Veikko Salomaa, Andrea Angius, Fabio Busonero, Francesco Cucca, Carlo Sidore, Josine L. Min, Nicholas J. Timpson, George Davey Smith, Laura J. Corbin, Seppo Koskinen, Veikko Salomaa, Scott Vrieze, Scott Vrieze, Cristen J. Willer, He Zhang, Jan H. Veldink, Wouter van Rheenen, Leonard H. van den Berg, Annelot M. Dekker, Tabitha A. Harrison, Charles Kooperberg, Ulrike Peters, Ulrike Peters, Michele T. Pato, Carlos N. Pato, Cornelia M. van Duijn, Matthew G. Sampson, Christopher E. Gillies, Nicola Pirastu, Ilaria Gandin, Massimiliano Cocca, Paolo Gasparini, Massimo Mezzavilla, Massimo Mezzavilla, Paolo Gasparini, Daniela Toniolo, Michela Traglia, Cinzia Sala, Dorrett Boomsma, Kari Branham, Gerome Breen, Gerome Breen, Chad M. Brummett, Ross M. Fraser, James F. Wilson, Harry Campbell, Andrew T. Chan, Andrew T. Chan, Cristen J. Willer, Matthias Kretzler, Sai Chen, Cristen J. Willer, Matthias Kretzler, Sai Chen, Emily Y. Chew, Francis S. Collins, George Dedoussis, Aliki‐Eleni Farmaki, Marcus Dörr, Matthias Nauck, Uwe Völker, Marcus Dörr and 11 more - Nature Genetics 2016 cited by 3,273

  2. An integrated map of structural variation in 2,504 human genomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Taejeong Bae, Eliza Cerveira, Peter S. Chines, Zechen Chong, Laura Clarke, Elif Dal, Li Ding, Sarah B. Emery, Xian Fan, Madhusudan Gujral, Fatma Kahveci, Jeffrey M. Kidd, Yu Kong, Eric-Wubbo Lameijer, Shane McCarthy, Paul Flicek, Richard A. Gibbs, Gábor Marth, Christopher E. Mason, Androniki Menelaou, Donna M. Muzny, Bradley J. Nelson, Amina Noor, Nicholas F. Parrish, Matthew Pendleton, Andrew Quitadamo, Benjamin Raeder, Eric E. Schadt, Mallory Romanovitch, Andreas Schlattl, Robert Sebra, Andrey A. Shabalin, Andreas Untergasser, Jerilyn A. Walker, Min Wang, Fuli Yu, Chengsheng Zhang, Jing Zhang, Xiangqun Zheng-Bradley, Wanding Zhou, Thomas Zichner, Jonathan Sebat, Mark A. Batzer, Steven A. McCarroll, Ryan E. Mills, Mark Gerstein, Ali Bashir, Oliver Stegle, Scott E. Devine, Charles Lee, Evan E. Eichler, Jan O. Korbel - Nature 2015 cited by 2,695

  3. An atlas of genetic influences on human blood metabolites

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , M. Julia Brosnan, Christian Gieger, Gabi Kastenmüller, Tim D. Spector, Nicole Soranzo - Nature Genetics 2014 cited by 1,645

  4. An integrated map of genetic variation from 1,092 human genomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mark A. DePristo, David Reich, Matthew E. Hurles, Senduran Balasubramaniam, John Burton, Petr Danecek, Thomas M. Keane, Mark A. DePristo, Shane McCarthy, James Stalker, Michael Quail, Robert E. Handsaker, Yuan Chen, Alison J. Coffey, Vincenza Colonna, Ni Huang, Luke Jostins, Aylwyn Scally, Klaudia Walter, Yali Xue, Yujun Zhang, Ben Blackburne, Sarah J. Lindsay, Zemin Ning, Adam Frankish, Jennifer Harrow, Richard M. Durbin, Chris Tyler-Smith, Gonçalo R. Abecasis, Richard Durbin, Tom Blackwell, Fabio Busonero, Christian Fuchsberger, Goo Jun, Andrea Maschio, Eleonora Porcu, Carlo Sidore, Adrian Tan, Mary Kate Trost, Hyun Min Kang, David R. Bentley, Russell Grocock, Gonçalo R. Abecasis, Jin Yu, Zoya Kingsbury, Jin Yu, R. Keira Cheetham, Tony Cox, Michael Eberle, Lisa Murray, Richard Shaw, Aravinda Chakravarti, Andrew G. Clark, Alon Keinan, Juan L. Rodriguez-Flores, Francisco M. De La Vega, Jeremiah Degenhardt, Evan E. Eichler, Paul Flicek, Laura Clarke, Rasko Leinonen, Richard E. Smith, Xiangqun Zheng-Bradley, Kathryn Beal, Fiona Cunningham, Javier Herrero, William M. McLaren, Graham R. S. Ritchie, Jonathan Barker, Gavin Kelman and 263 more - Nature 2012 cited by 8,269

  5. The Polygenic and Monogenic Basis of Blood Traits and Diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter W.F. Wilson, Hélène Choquet, John Danesh, Emanuele Di Angelantonio, Niki Dimou, Jingzhong Ding, Paul Elliott, Tõnu Esko, Michele K. Evans, Stephan B. Felix, James S. Floyd, Linda Broer, Niels Grarup, Michael H. Guo, Qi Guo, Andreas Greinacher, Jeff Haessler, Torben Hansen, Joanna M. M. Howson, Wei Huang, Eric Jorgenson, Tim Kacprowski, Mika Kähönen, Yoichiro Kamatani, Masahiro Kanai, Savita Karthikeyan, Fotios Koskeridis, Leslie A. Lange, Terho Lehtimäki, Allan Linneberg, Yongmei Liu, Leo‐Pekka Lyytikäinen, Ani Manichaikul, Koichi Matsuda, Karen L. Mohlke, Nina Mononen, Yoshinori Murakami, Girish N. Nadkarni, Kjell Nikus, Nathan Pankratz, Oluf Pedersen, Michael Preuß, Bruce M. Psaty, Olli T. Raitakari, Stephen S. Rich, Blanca Rodríguez, Jonathan D. Rosen, Jerome I. Rotter, Petra Schubert, Cassandra N. Spracklen, Praveen Surendran, Hua Tang, Jean‐Claude Tardif, Mohsen Ghanbari, Uwe Völker, Henry Völzke, Nicholas A. Watkins, Stefan Weiß, Na Cai, Kousik Kundu, Stephen B. Watt, Klaudia Walter, Alan B. Zonderman, Kelly Cho, Yun Li, Ruth J. F. Loos, Julian C. Knight, Michel Georges, Oliver Stegle, Εvangelos Εvangelou and 12 more - Cell 2020 cited by 756

  6. Accurate whole human genome sequencing using reversible terminator chemistry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Isabelle Rasolonjatovo, Mark T. Reed, Roberto Rigatti, Chiara Rodighiero, Mark T. Ross, Andrea Sabot, S. V. Sankar, Aylwyn Scally, Gary P. Schroth, Mark E. B. Smith, Vincent P. Smith, Anastassia Spiridou, Peta E. Torrance, Svilen Tzonev, Eric H. Vermaas, Klaudia Walter, Xiaolin Wu, Lu Zhang, Mohammed D. Alam, Carole Anastasi, Ify C. Aniebo, David M. Bailey, Iain R. Bancarz, Saibal Banerjee, Selena G. Barbour, Primo Baybayan, Vincent A. Benoit, Kevin F. Benson, Claire Bevis, Phillip J. Black, Asha Boodhun, Joe S. Brennan, John A. Bridgham, Rob Brown, Andrew Brown, Dale H. Buermann, Abass A. Bundu, James C. Burrows, Nigel P. Carter, Néstor Castillo-Magallanes, Maria Chiara E. Catenazzi, Simon Chang, Rachel Cooley, Natasha R. Crake, Olubunmi O. Dada, Konstantinos D. Diakoumakos, Belen Dominguez‐Fernandez, David Earnshaw, Ugonna C. Egbujor, David W. Elmore, Sergey S. Etchin, Mark Ewan, Milan Fedurco, Louise Fraser, Karin V. Fuentes Fajardo, W. Scott Furey, David George, Kimberley J. Gietzen, C Goddard, George S. Golda, Philip A. Granieri, David E. Green, David Gustafson, Nancy F. Hansen, Kevin Harnish, Christian Haudenschild, Narinder I. Heyer, Matthew M. Hims, Johnny T. Ho, Adrian Horgan and 94 more - Nature 2008 cited by 3,798

  7. The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joost H.A. Martens, Stuart Meacham, Karyn Mégy, Jared O’Connell, R. Petersen, Nilofar Sharifi, Simon Sheard, James R Staley, Salih Tuna, Martijn van der Ent, Klaudia Walter, Shuang-Yin Wang, Eleanor Wheeler, Steven P. Wilder, Valentina Iotchkova, Carmel Moore, Jennifer Sambrook, Hendrik G. Stunnenberg, Emanuele Di Angelantonio, Stephen Kaptoge, Taco W. Kuijpers, Enrique Carrillo de Santa Pau, David Juan, Daniel Rico, Alfonso Valencia, Lu Chen, Bing Ge, Louella Vasquez, Tony Kwan, Diego Garrido-Martín, Stephen Watt, Ying Yang, Roderic Guigó, Stephan Beck, Dirk S. Paul, Tomi Pastinen, David Bujold, Guillaume Bourque, Mattia Frontini, John Danesh, David J. Roberts, Willem H. Ouwehand, Adam S. Butterworth, Nicole Soranzo - Cell 2016 cited by 1,425

  8. The UK10K project identifies rare variants in health and disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 249 more - Nature 2015 cited by 1,195

  9. Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Maxime Caron, Shu‐Huang Chen, Warren Cheung, Oliver Delaneau, Emmanouil T. Dermitzakis, Heather Elding, Irina Colgiu, Frederik Otzen Bagger, Paul Flicek, Ehsan Habibi, Valentina Iotchkova, Eva M. Janssen‐Megens, Bowon Kim, Hans Lehrach, Ernesto Lowy, Amit Mandoli, Filomena Matarese, Matthew T. Maurano, John Morris, Véra Pancaldi, Farzin Pourfarzad, Karola Rehnström, Augusto Rendon, Thomas S. Risch, Nilofar Sharifi, Marie-Michelle Simon, Marc Sultan, Alfonso Valencia, Klaudia Walter, Shuang-Yin Wang, Mattia Frontini, Stylianos E. Antonarakis, Laura Clarke, Marie‐Laure Yaspo, Stephan Beck, Roderic Guigó, Daniel Rico, Joost H.A. Martens, Willem H. Ouwehand, Taco W. Kuijpers, Dirk S. Paul, Hendrik G. Stunnenberg, Oliver Stegle, Kate Downes, Tomi Pastinen, Nicole Soranzo - Cell 2016 cited by 790

  10. A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , If Barnes, Clara Amid, Denise Carvalho‐Silva, Alexandra Bignell, Catherine Snow, Bryndís Yngvadóttir, Suzannah Bumpstead, D.N. Cooper, Yali Xue, Irene Gallego Romero, Jun Wang, Yingrui Li, Richard A. Gibbs, Steven A. McCarroll, Emmanouil T. Dermitzakis, Jonathan K. Pritchard, Jeffrey C. Barrett, Jennifer Harrow, Matthew E. Hurles, Mark Gerstein, Chris Tyler‐Smith - Science 2012 cited by 1,349

  11. Mapping copy number variation by population-scale genome sequencing

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ruibang Luo, Xinmeng Jasmine Mu, James Nemesh, Heather E. Peckham, Tobias Rausch, Aylwyn Scally, Xinghua Shi, Michael P. Strömberg, Adrian M. Stütz, Alexander E. Urban, Jerilyn A. Walker, Jiantao Wu, Yujun Zhang, Zhengdong D. Zhang, Mark A. Batzer, Li Ding, Gábor Marth, Gil McVean, Jonathan Sebat, M Snyder, Jun Wang, Kenny Ye, Evan E. Eichler, Mark Gerstein, Matthew E. Hurles, Charles Lee, Steven A. McCarroll, Jan O. Korbel - Nature 2011 cited by 1,215

  12. Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lauren E. Mokry, Alireza Moayyeri, Melina Claussnitzer, Chia‐Ho Cheng, Warren Cheung, Carolina Medina‐Gómez, Bing Ge, Shu‐Huang Chen, Kwangbom Choi, Ling Oei, James A. Fraser, Robert Kraaij, Matthew Hibbs, Celia L. Gregson, Denis Paquette, Albert Hofman, Carl Wibom, Gregory J. Tranah, Mhairi Marshall, Brooke Gardiner, Katie Cremin, Paul L. Auer, Li Hsu, Sue Ring, Joyce Y. Tung, Gudmar Thorleifsson, Anke W. Enneman, Natasja M. van Schoor, C.P.G.M. de Groot, Nathalie van der Velde, Beatrice Melin, John P. Kemp, Claus Christiansen, Adrian Sayers, Yanhua Zhou, Sophie Caldérari, Jeroen van Rooij, Chris Carlson, Ulrike Peters, Soizik Berlivet, Josée Dostie, André G. Uitterlinden, Stephen R. Williams, Charles R. Farber, Daniel Grinberg, Andrea Z. LaCroix, Jeff Haessler, Daniel I. Chasman, Franco Giulianini, Lynda M. Rose, Paul M. Ridker, John A. Eisman, Tuan V. Nguyen, Xavier Nogués, Natalia García‐Giralt, Lenore L. Launer, Vilmunder Gudnason, Dan Mellström, Liesbeth Vandenput, Najaf Amin, Cornelia M. van Duijn, Magnus K. Karlsson, Östen Ljunggren, Olle Svensson, Göran Hallmans, François Rousseau, Sylvie Giroux, Johanne Bussière, Pascal Arp, Fjorda Koromani and 55 more - Nature 2015 cited by 637

  13. Origins and functional impact of copy number variation in the human genome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2009 cited by 2,062

  14. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Juan P. Casas, John C. Chambers, Ruth Charlton, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebahattin Çırak, Peter Clapham, Gail Clement, Guy Coates, Massimiliano Cocca, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Ian N.M. Day, Aaron Day-Williams, George Dedoussis, Thomas A. Down, Yuanping Du, Cornelia M. van Duijn, Ian Dunham, Sarah Edkins, Rosemary Ekong, Peter Ellis, David M. Evans, I. Sadaf Farooqi, David Fitzpatrick, Paul Flicek, James Floyd, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Paolo Gasparini, Tom R. Gaunt, Matthias Geihs, Daniel H. Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xiaosen Guo, Xueqin Guo, Hugh Gurling, Deborah Hart, Audrey E. Hendricks, Peter Holmans, Liren Huang, Tim Hubbard, Steve E. Humphries, Matthew E. Hurles, Pirro G. Hysi, Valentina Iotchkova, Aaron Isaacs, David K. Jackson, Yalda Jamshidi, Jon Johnson, Christopher Joyce, Konrad J. Karczewski, Jane Kaye, Thomas Keane, John P. Kemp and 139 more - Nature Communications 2015 cited by 385

  15. Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 285 more - Nature Communications 2014 cited by 457

  16. GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals

    Authors: , , , , , , , , , - Nature Genetics 2019 cited by 223

  17. The impact of rare and low-frequency genetic variants in common disease

    Authors: , , - Genome biology 2017 cited by 367

  18. The Polygenic and Monogenic Basis of Blood Traits and Diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kelly Cho, Hélène Choquet, Adolfo Correa, John Danesh, Emanuele Di Angelantonio, Niki Dimou, Jingzhong Ding, Paul Elliott, Tõnu Esko, Michele K. Evans, Stephan B. Felix, James S. Floyd, Linda Broer, Niels Grarup, Michael H. Guo, Andreas Greinacher, Jeff Haessler, Torben Hansen, Joanna M. M. Howson, Wei Huang, Eric Jorgenson, Tim Kacprowski, Mika Kähönen, Yoichiro Kamatani, Masahiro Kanai, Savita Karthikeyan, Fotis Koskeridis, Leslie A. Lange, Terho Lehtimäki, Allan Linneberg, Yongmei Liu, Leo‐Pekka Lyytikäinen, Ani Manichaikul, Koichi Matsuda, Karen L. Mohlke, Nina Mononen, Yoshinori Murakami, Girish N. Nadkarni, Kjell Nikus, Nathan Pankratz, Oluf Pedersen, Michael Preuß, Bruce M. Psaty, Olli T. Raitakari, Stephen S. Rich, Benjamin A.T. Rodriguez, Jonathan D. Rosen, Jerome I. Rotter, Petra Schubert, Cassandra N. Spracklen, Praveen Surendran, Hua Tang, Jean‐Claude Tardif, Mohsen Ghanbari, Uwe Völker, Henry Völzke, Nicholas A. Watkins, Stefan Weiß, VA Million Veteran Program, Na Cai, Kousik Kundu, Stephen B. Watt, Klaudia Walter, Alan B. Zonderman, Peter W.F. Wilson, Yun Li, Ruth J. F. Loos, Julian C. Knight, Michel Georges, Oliver Stegle and 13 more - medRxiv 2020 cited by 65

  19. Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2021 cited by 76

  20. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hashem A. Shihab, Lorraine Southam, Beaté St Pourcain, Michela Traglia, Katerina Trajanoska, Gialuigi Zaza, Weihua Zhang, María Soler Artigas, Narinder Bansal, Marianne Benn, Zhongsheng Chen, Petr Danecek, Wei‐Yu Lin, Adam E. Locke, Jian’an Luan, Alisa K. Manning, Antonella Mulas, Carlo Sidore, Anne Tybjærg‐Hansen, Anette Varbo, Magdalena Żołędziewska, Chris Finan, Konstantinos Hatzikotoulas, Audrey E. Hendricks, John P. Kemp, Alireza Moayyeri, Kalliope Panoutsopoulou, Michał Szpak, Scott G. Wilson, Michael Boehnke, Francesco Cucca, Emanuele Di Angelantonio, Claudia Langenberg, Cecilia M. Lindgren, Mark I. McCarthy, Andrew P. Morris, Børge G. Nordestgaard, Robert A. Scott, Martin D. Tobin, Nicholas J. Wareham, Paul R. Burton, John C. Chambers, George Davey Smith, George Dedoussis, Janine F. Felix, Oscar H. Franco, Giovanni Gambaro, Paolo Gasparini, Christopher J. Hammond, Albert Hofman, Vincent W. V. Jaddoe, Marcus E. Kleber, Jaspal S. Kooner, Markus Perola, Caroline L. Relton, Susan M. Ring, Fernando Rivadeneira, Veikko Salomaa, Timothy D. Spector, Oliver Stegle, Daniela Toniolo, André G. Uitterlinden, Inês Barroso, Celia M.T. Greenwood, John R. B. Perry, Brian R. Walker, Adam S. Butterworth, Yali Xue, Richard Durbin, Kerrin S. Small and 3 more - The American Journal of Human Genetics 2017 cited by 218

  21. Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates

    Authors: , , , , , , , , , , , , , , - International Journal of Obesity 2021 cited by 79

  22. Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases

    Authors: , , , , , , , , , , , , , - Nature Genetics 2022 cited by 73

  23. Genetic basis of early onset and progression of type 2 diabetes in South Asians

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Karen A. Hunt, Matt Hurles, Shapna Hussain, Kamrul Islam, Vivek Iyer, Georgios Kalantzis, Ahsan Khan, Cath Lavery, Sang Hyuck Lee, Daniel G. MacArthur, Eamonn Maher, Daniel Malawsky, Sidra Malik, Hilary C. Martin, Dan Mason, Mohammed Bodrul Mazid, John McDermott, Caroline E Morton, Bill Newman, Vladimir Ovchinnikov, Elizabeth Owor, Iaroslav Popov, Asma Qureshi, Mehru Raza, Jessry Russell, Stuart Rison, Nishat Safa, Annum Salman, Michael A. Simpson, John Solly, Michael D. Taylor, Richard C. Trembath, Karen Tricker, David A. van Heel, Klaudia Walter, Jan Whalley, Caroline Winckley, S. M. Wood, John Wright, Sabina Yasmin, Ishevanhu Zengeya, Claudia Langenberg, David A. van Heel, Rohini Mathur, Moneeza K. Siddiqui, Sarah Finer - Nature Medicine 2024 cited by 38

  24. Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development

    Authors: , , , , , , , , , , , , , , , - PLoS Biology 2004 cited by 987