Paul L. Auer

Active 2010–2025

119
Papers
21,201
Citations
64
h-index
112
i10-index

Citations

Citations per year for Paul L. Auer1972: 1 citations1987: 1 citations1991: 4 citations2000: 1 citations2003: 3 citations2004: 2 citations2007: 1 citations2010: 1 citations2011: 15 citations2012: 16 citations2013: 36 citations2014: 53 citations2015: 112 citations2016: 120 citations2017: 197 citations2018: 234 citations2019: 779 citations2020: 921 citations2021: 1,062 citations2022: 1,100 citations2023: 872 citations2024: 1,269 citations2025: 624 citations2026: 35 citations1973–1986: no citations, so these years are not shown1988–1990: no citations, so these years are not shown1992–1999: no citations, so these years are not shown2001–2002: no citations, so these years are not shown2005–2006: no citations, so these years are not shown2008–2009: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,205 citing papers, 20.8% of this breakdownUnited Kingdom: 1,342 citing papers, 8.7% of this breakdownChina: 981 citing papers, 6.4% of this breakdownGermany: 763 citing papers, 5% of this breakdownCanada: 682 citing papers, 4.4% of this breakdownAustralia: 586 citing papers, 3.8% of this breakdownNetherlands: 556 citing papers, 3.6% of this breakdownSweden: 499 citing papers, 3.2% of this breakdownItaly: 492 citing papers, 3.2% of this breakdownFrance: 479 citing papers, 3.1% of this breakdownSpain: 389 citing papers, 2.5% of this breakdownDenmark: 365 citing papers, 2.4% of this breakdown
0%20.8%Other 32.9%

Fields

  • Biochemistry, Genetics and Molecular Biology55.5%
  • Medicine34.5%
  • Neuroscience2.2%
  • Immunology and Microbiology2%
  • Agricultural and Biological Sciences1.3%
  • Computer Science1.2%
  • Other3.3%

Topics

  • Genetic Associations and Epidemiology11.8%
  • BRCA gene mutations in cancer3.7%
  • Genomics and Rare Diseases3.5%
  • Bioinformatics and Genomic Networks2.2%
  • Genetic Mapping and Diversity in Plants and Animals2.1%
  • Cancer Genomics and Diagnostics1.9%
  • Other74.8%

Coauthors

All papers

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  1. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dan E. Arking, Stella Aslibekyan, Paul L. Auer, John Barnard, R. Graham Barr, Lucas Barwick, Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Daniel I. Chasman, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie S. Emery, Celeste Eng, Diane Fatkin, Tasha E. Fingerlin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos and 325 more - Nature 2021 cited by 2,355

  2. Association analysis identifies 65 new breast cancer risk loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Habibul Ahsan, Kristiina Aittomäki, Hoda Anton‐Culver, Natalia Antonenkova, Volker Arndt, Kristan J. Aronson, Banu Arun, Paul L. Auer, François Bacot, Myrto Barrdahl, Caroline Baynes, Matthias W. Beckmann, Sabine Behrens, Javier Benı́tez, Marina Bermisheva, Leslie Bernstein, Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Judith S. Brand, Hiltrud Brauch, Paul Brennan, Hermann Brenner, Louise A. Brinton, Per Broberg, Ian W. Brock, Annegien Broeks, Angela Brooks‐Wilson, Sara Y. Brucker, Thomas Brüning, Barbara Burwinkel, Katja Butterbach, Qiuyin Cai, Hui Cai, Trinidad Caldés, Federico Canzian, Ángel Carracedo, Brian D. Carter, Jose E. Castelao, Tsun Leung Chan, Ting‐Yuan David Cheng, Kee Seng Chia, Ji‐Yeob Choi, Hans Christiansen, Christine L. Clarke, NBCS Collaborators, Margriet Collée, Don Conroy, Emilie Cordina‐Duverger, Sten Cornelissen, David G. Cox, Angela Cox, Simon S. Cross, Julie M. Cunningham, Kamila Czene, Mary B. Daly, Peter Devilee, Kimberly F. Doheny, Thilo Dörk, Isabel dos‐Santos‐Silva, Martine Dumont, Lorraine Durcan, Miriam Dwek, Diana M. Eccles, Arif B. Ekici, A. Heather Eliassen, Carolina Ellberg, Mingajeva Elvira and 262 more - Nature 2017 cited by 1,598

  3. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Natalia Bogdanova, Stig E. Bojesen, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Hiltrud Brauch, Michael Bremer, Hermann Brenner, Adam R. Brentnall, Ian W. Brock, Angela Brooks‐Wilson, Sara Y. Brucker, Thomas Brüning, Barbara Burwinkel, Daniele Campa, Brian D. Carter, Jose E. Castelao, Stephen J. Chanock, Rowan T. Chlebowski, Hans Christiansen, Christine L. Clarke, J. Margriet Collée, Emilie Cordina‐Duverger, Sten Cornelissen, Fergus J. Couch, Angela Cox, Simon S. Cross, Kamila Czene, Mary B. Daly, Peter Devilee, Thilo Dörk, Isabel dos‐Santos‐Silva, Martine Dumont, Lorraine Durcan, Miriam Dwek, Diana M. Eccles, Arif B. Ekici, A. Heather Eliassen, Carolina Ellberg, Christoph Engel, Mikael Eriksson, D. Gareth Evans, Peter A. Fasching, Jonine D. Figueroa, Olivia Fletcher, Henrik Flyger, Asta Försti, Lin Fritschi, Marike Gabrielson, Manuela Gago-Domínguez, Susan M. Gapstur, José Á. García-Sáenz, Mia M. Gaudet, V. Georgoulias, Graham G. Giles, I. R. Gilyazova, Gord Glendon, Mark S. Goldberg, David E. Goldgar, Anna González‐Neira, Grethe I.G. Alnæs, Mervi Grip, Jacek Gronwald, Anne Grundy, Pascal Guénel, Lothar Haeberle, Eric Hahnen, Christopher A. Haiman, Niclas Håkansson, Ute Hamann, Susan E. Hankinson and 169 more - The American Journal of Human Genetics 2018 cited by 1,183

  4. A Population-Based Study of Genes Previously Implicated in Breast Cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Loı̈c Le Marchand, Sara Lindströem, Tricia Lindstrom, Huiyan Ma, Susan L. Neuhausen, Polly A. Newcomb, Katie M. O’Brien, Janet E. Olson, Irene M. Ong, Tuya Pal, Julie R. Palmer, Alpa V. Patel, Sonya Reid, Lynn Rosenberg, Dale P. Sandler, Christopher J. Scott, Rulla M. Tamimi, Jack A. Taylor, Amy Trentham‐Dietz, Celine M. Vachon, Clarice R. Weinberg, Song Yao, Argyrios Ziogas, Jeffrey N. Weitzel, David E. Goldgar, Susan M. Domchek, Katherine L. Nathanson, Peter Kraft, Eric C. Polley, Fergus J. Couch - New England Journal of Medicine 2021 cited by 866

  5. Principles and methods for transferring polygenic risk scores across global populations

    Authors: , , , , , , , , , , , , , , , , - Nature Reviews Genetics 2023 cited by 313

  6. Clonal haematopoiesis and risk of chronic liver disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Raymond T. Chung, Kathleen E. Corey, Daniel Levy, Christie M. Ballantyne, NHLBI TOPMed Hematology Working Group, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Nathan R. Blue, Donald W. Bowden, Russell P. Bowler, Jennifer A. Brody, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban G. Burchard, Carlos D. Bustamante, Erin Buth, Brian E. Cade, Jonathan Cardwell, Vincent J. Carey, Julie Carrier, April P. Carson, Cara L. Carty, Richard Casaburi, Juan P. Romero, James F. Casella, Peter J. Castaldi, Mark Chaffin, Christy Chang, Yi‐Cheng Chang, Daniel I. Chasman, Sameer Chavan, Bo-Juen Chen and 340 more - Nature 2023 cited by 201

  7. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Bernardo Bonanni, Davide Bondavalli, Åke Borg, Hiltrud Brauch, Hermann Brenner, Ignacio Briceño, Annegien Broeks, Sara Y. Brucker, Thomas Brüning, Barbara Burwinkel, Saundra S. Buys, Helen Byers, Trinidad Caldés, Maria A. Caligo, Mariarosaria Calvello, Daniele Campa, Jose E. Castelao, Jenny Chang‐Claude, Stephen J. Chanock, Melissa Christiaens, Hans Christiansen, Wendy K. Chung, Kathleen Claes, Christine L. Clarke, Sten Cornelissen, Fergus J. Couch, Angela Cox, Simon S. Cross, Kamila Czene, Mary B. Daly, Peter Devilee, Orland Dı́ez, Susan M. Domchek, Thilo Dörk, Miriam Dwek, Diana M. Eccles, Arif B. Ekici, D. Gareth Evans, Peter A. Fasching, Jonine D. Figueroa, Lenka Foretová, Florentia Fostira, Eitan Friedman, Debra Frost, Manuela Gago-Domínguez, Susan M. Gapstur, Judy E. Garber, José Á. García-Sáenz, Mia M. Gaudet, Simon A. Gayther, Graham G. Giles, Andrew K. Godwin, Mark S. Goldberg, David E. Goldgar, Anna González‐Neira, Mark H. Greene, Jacek Gronwald, Pascal Guénel, Lothar Häberle, Eric Hahnen, Christopher A. Haiman, Christopher R. Hake, Per Hall, Ute Hamann, Elaine F. Harkness, Bernadette A. M. Heemskerk‐Gerritsen, Peter Hillemanns and 176 more - Nature Genetics 2020 cited by 567

  8. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xihao Li, Zilin Li, Elise Lim, D. Y. Lin, Xihong Lin, Simin Liu, Yingchang Lu, JoAnn E. Manson, Lisa W. Martin, Caitlin McHugh, Julie Mikulla, Solomon K. Musani, Maggie Ng, Deborah A. Nickerson, Nicholette Palmer, James A. Perry, Ulrike Peters, Michael Preuß, Qibin Qi, Laura M. Raffield, Laura J. Rasmussen‐Torvik, Alex P. Reiner, Emily M. Russell, Colleen M. Sitlani, Jennifer A. Smith, Cassandra N. Spracklen, Tao Wang, Zhe Wang, Jennifer Wessel, Hanfei Xu, Mohammad Yaser, Sachiko Yoneyama, Kendra A. Young, Jingwen Zhang, Xinruo Zhang, Hufeng Zhou, Xiaofeng Zhu, Sebastian Zoellner, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis and 360 more - Nature Genetics 2022 cited by 359

  9. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie S. Emery, Diane Fatkin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos, Lori Garman, Robert E. Gerszten, Steven A. Lubitz, Kathryn L. Lunetta, Angel C. Y. Mak, Ani Manichaikul, Alisa K. Manning, Rasika A. Mathias, David D. McManus, Stephen T. McGarvey and 78 more - 2019 cited by 423

  10. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gonçalo R. Abecasis, Katja K.H. Aben, Dewan S Alam, Sameer Alharthi, Matthew Allison, Philippe Amouyel, Folkert W. Asselbergs, Paul L. Auer, Beverley Balkau, Lia E. Bang, Inês Barroso, Lisa Bastarache, Marianne Benn, Sven Bergmann, Lawrence F. Bielak, Matthias Blüher, Michael Boehnke, Heiner Boeing, Eric Boerwinkle, Carsten A. Böger, Jette Bork‐Jensen, Michiel L. Bots, Erwin P. Böttinger, Donald W. Bowden, Ivan Brandslund, Gerome Breen, Murray H. Brilliant, Linda Broer, Marco Brumat, Amber Burt, Adam S. Butterworth, Peter T. Campbell, Stefania Cappellani, David J. Carey, Eulalia Catamo, Mark J. Caulfield, John C. Chambers, Daniel I. Chasman, Yii‐Der Ida Chen, Rajiv Chowdhury, Cramer Christensen, Audrey Y. Chu, Massimiliano Cocca, Francis S. Collins, James P. Cook, Janie Corley, Jordi Corominas Galbany, Amanda J. Cox, David S. Crosslin, Gabriel Cuéllar-Partida, Angela D’Eustacchio, John Danesh, Gail Davies, Paul I. W. de Bakker, Mark de Groot, Renée de Mutsert, Ian J. Deary, George Dedoussis, Ellen W. Demerath, Martin den Heijer, Anneke I. den Hollander, Hester M. den Ruijter, Joe Dennis, Joshua C. Denny, Emanuele Di Angelantonio, Fotios Drenos, Mengmeng Du, Marie‐Pierre Dubé, Alison M. Dunning, Douglas F. Easton and 304 more - Nature Genetics 2017 cited by 428

  11. A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yukinori Okada, Buhm Han, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Eric Boerwinkle, Donald W. Bowden, Russell P. Bowler, Jennifer A. Brody, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban Burchard, Carlos D. Bustamante, Erin Buth, Brian E. Cade, Jonathan Cardwell, Vincent J. Carey, Julie Carrier, Cara L. Carty, Richard Casaburi, Juan P. Romero, James F. Casella, Peter J. Castaldi, Mark Chaffin, Christy Chang, Yi‐Cheng Chang, Daniel I. Chasman, Sameer Chavan, Bo‐Juen Chen, Wei‐Min Chen, Seung Hoan Choi, Lee‐Ming Chuang, Mina K. Chung and 332 more - Nature Genetics 2021 cited by 187

  12. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael C. Mahaney, Ani Manichaikul, Lisa W. Martin, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, May E. Montasser, Jill E. Moore, Alanna C. Morrison, Jeffrey R. O’Connell, Nicholette D. Palmer, Akhil Pampana, Juan M. Peralta, Patricia A. Peyser, Bruce M. Psaty, Susan Redline, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Hemant K. Tiwari, Michael Y. Tsai, Ramachandran S. Vasan, Fei Fei Wang, Daniel E. Weeks, Zhiping Weng, James G. Wilson, Lisa R. Yanek, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Lawrence F. Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Eric Boerwinkle, Donald W. Bowden, Russell P. Bowler, Jennifer Brody, Ulrich Broeckel, Jai Broome, Karen Bunting and 459 more - Nature Genetics 2020 cited by 290

  13. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jamie Allen, Christine B. Ambrosone, Christopher I. Amos, Irene L. Andrulis, Hoda Anton‐Culver, Natalia Antonenkova, Volker Arndt, Norbert Arnold, Kristan J. Aronson, Bernd Auber, Paul L. Auer, Margreet G.E.M. Ausems, Jacopo Azzollini, François Bacot, Judith Balmañà, Monica Barile, Laure Barjhoux, Rósa B. Barkardóttir, Myrto Barrdahl, Daniel R. Barnes, Daniel Barrowdale, Caroline Baynes, Matthias W. Beckmann, Javier Benı́tez, Marina Bermisheva, Leslie Bernstein, Yves‐Jean Bignon, Kathleen R. Blazer, Marinus J. Blok, Carl Blomqvist, William J. Blot, Kristie Bobolis, Bram Boeckx, Natalia Bogdanova, Anders Bojesen, Stig E. Bojesen, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Anikó Bozsik, Angela R. Bradbury, Judith S. Brand, Hiltrud Brauch, Hermann Brenner, Brigitte Bressac–de Paillerets, Carole Brewer, Louise A. Brinton, Per Broberg, Angela Brooks‐Wilson, Joan Brunet, Thomas Brüning, Barbara Burwinkel, Saundra S. Buys, Jinyoung Byun, Qiuyin Cai, Trinidad Caldés, Maria A. Caligo, Ian Campbell, Federico Canzian, Olivier Caron, Ángel Carracedo, Brian D. Carter, Jose E. Castelao, Laurent Castéra, Virginie Caux‐Moncoutier, Salina Chan, Jenny Chang‐Claude, Stephen J. Chanock, Xiaoqing Chen, Ting‐Yuan David Cheng, Jocelyne Chiquette and 376 more - Nature Genetics 2017 cited by 471

  14. 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

  15. Comparison of Proteomic Assessment Methods in Multiple Cohort Studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jerome I. Rotter, Paul L. Auer, Alex P. Reiner, Russell P. Tracy, Debby Ngo, Robert E. Gerszten, Wanda K. O’Neal, Russell P. Bowler - PROTEOMICS 2020 cited by 185

  16. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jessica D. Faul, Eric B. Fauman, Cristiano Fava, Teresa Ferreira, Christopher N. Foley, Nora Franceschini, He Gao, Olga Giannakopoulou, Franco Giulianini, Daníel F. Guðbjartsson, Xiuqing Guo, Sarah E. Harris, Aki S. Havulinna, Anna Helgadóttir, Jennifer E. Huffman, Shih‐Jen Hwang, Stavroula Kanoni, Jukka Kontto, Martin G. Larson, Ruifang Li‐Gao, Jaana Lindström, Luca A. Lotta, Yingchang Lu, Jian’an Luan, Anubha Mahajan, Giovanni Malerba, Nicholas G. D. Masca, Hao Mei, Cristina Menni, Dennis O. Mook‐Kanamori, David Mosén-Ansorena, Martina Müller‐Nurasyid, Guillaume Paré, Dirk S. Paul, Markus Perola, Alaitz Poveda, Rainer Rauramaa, Melissa A. Richard, Tom G. Richardson, Nuno Sepúlveda, Xueling Sim, Albert V. Smith, Jennifer A. Smith, James R Staley, Alena Stanáková, Patrick Sulem, Sébastien Thériault, Unnur Þorsteinsdóttir, Stella Trompet, Tibor V. Varga, Digna R. Velez Edwards, Giovanni Veronesi, Stefan Weiß, Sara M. Willems, Jie Yao, Robin Young, Bing Yu, Weihua Zhang, Jinghua Zhao, Wei Zhao, Wei Zhao, Εvangelos Εvangelou, Stefanie Aeschbacher, Eralda Asllanaj, Stefan Blankenberg, Lori L. Bonnycastle, Jette Bork‐Jensen, Ivan Brandslund, Peter S. Braund, Stephen Burgess and 212 more - Nature Genetics 2020 cited by 239

  17. Identification of nine new susceptibility loci for endometrial cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jennifer A. Doherty, Thilo Dörk, Sean C. Dowdy, Matthias Dürst, Arif B. Ekici, Peter A. Fasching, Brooke L. Fridley, Christine M. Friedenreich, Lin Fritschi, Jenny N. Fung, Montserrat García‐Closas, Mia M. Gaudet, Graham G. Giles, Ellen L. Goode, Maggie Gorman, Christopher A. Haiman, Per Hall, Susan E. Hankison, Catherine S. Healey, Alexander Hein, Peter Hillemanns, Shirley Hodgson, Erling A. Høivik, Elizabeth Holliday, John L. Hopper, David J. Hunter, Angela Jones, Camilla Krakstad, Vessela N. Kristensen, Diether Lambrechts, Loı̈c Le Marchand, Xiaolin Liang, Annika Lindblom, Jolanta Lissowska, Jirong Long, Lingeng Lu, Anthony M. Magliocco, Lynn Martin, Mark McEvoy, Alfons Meindl, Kyriaki Michailidou, Roger L. Milne, Miriam Mints, Grant W. Montgomery, Rami Nassir, Håkan Olsson, Irene Orlow, Geoffrey Otton, Claire Palles, John R. B. Perry, Julian Peto, Loreall Pooler, Jennifer Prescott, Tony Proietto, Timothy R. Rebbeck, Harvey A. Risch, Peter A. W. Rogers, Matthias Rübner, Ingo B. Runnebaum, Carlotta Sacerdote, Gloria E. Sarto, Fredrick R. Schumacher, Rodney J. Scott, Veronica Wendy Setiawan, Mitul Shah, Xin Sheng, Xiao‐Ou Shu, Melissa C. Southey, Anthony J. Swerdlow, Emma Tham and 25 more - Nature Communications 2018 cited by 326

  18. Rare and low-frequency coding variants alter human adult height

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Linda S. Adair, Dewan S Alam, Eva Albrecht, Kristine H. Allin, Matthew Allison, Philippe Amouyel, Emil V. R. Appel, Dominique Arveiler, Folkert W. Asselbergs, Paul L. Auer, Beverley Balkau, Bernhard Banas, Lia E. Bang, Marianne Benn, Sven Bergmann, Lawrence F. Bielak, Matthias Blüher, Heiner Boeing, Eric Boerwinkle, Carsten A. Böger, Lori L. Bonnycastle, Jette Bork‐Jensen, Michiel L. Bots, Erwin P. Böttinger, Donald W. Bowden, Ivan Brandslund, Gerome Breen, Murray H. Brilliant, Linda Broer, Amber Burt, Adam S. Butterworth, David J. Carey, Mark J. Caulfield, John C. Chambers, Daniel I. Chasman, Yii‐Der Ida Chen, Rajiv Chowdhury, Cramer Christensen, Audrey Y. Chu, Massimiliano Cocca, Francis S. Collins, James P. Cook, Janie Corley, Jordi Corominas Galbany, Amanda J. Cox, Gabriel Cuéllar-Partida, John Danesh, Gail Davies, Paul I. W. de Bakker, Gert J. de Borst, Simon de Denus, Mark de Groot, Renée de Mutsert, Ian J. Deary, George Dedoussis, Ellen W. Demerath, Anneke I. den Hollander, Joe Dennis, Emanuele Di Angelantonio, Fotios Drenos, Mengmeng Du, Alison M. Dunning, Douglas F. Easton, Tapani Ebeling, Todd L. Edwards, Patrick T. Ellinor, Paul Elliott, Εvangelos Εvangelou, Aliki‐Eleni Farmaki, Jessica D. Faul and 273 more - Nature 2017 cited by 666

  19. Exome-wide association study of plasma lipids in >300,000 individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , John C. Chambers, Daniel I. Chasman, Y Eugene Chen, Yii‐Der Ida Chen, Rajiv Chowdhury, Cramer Christensen, Audrey Y. Chu, John Connell, Francesco Cucca, L. Adrienne Cupples, Scott M. Damrauer, Gail Davies, Ian J. Deary, George Dedoussis, Joshua C. Denny, Anna F. Dominiczak, Marie‐Pierre Dubé, Tapani Ebeling, Guðný Eiríksdóttir, Tõnu Esko, Aliki‐Eleni Farmaki, Mary F. Feitosa, Maurizio Ferrario, Jean Ferrières, Ian Ford, Myriam Fornage, Paul W. Franks, Timothy M. Frayling, Ruth Frikke‐Schmidt, Lars G. Fritsche, Philippe Frossard, Valentı́n Fuster, Santhi K. Ganesh, Wei Gao, Melissa E. Garcia, Christian Gieger, Franco Giulianini, Mark O. Goodarzi, Harald Grallert, Niels Grarup, Leif Groop, Megan L. Grove, Vilmundur Guðnason, Torben Hansen, Tamara B. Harris, Caroline Hayward, Joel N. Hirschhorn, Oddgeir L. Holmen, Jennifer E. Huffman, Yong Huo, Kristian Hveem, Sehrish Jabeen, Anne Jackson, Jóhanna Jakobsdóttir, Marjo‐Riitta Järvelin, Gorm Boje Jensen, Marit E. Jørgensen, J. Wouter Jukema, Johanne Marie Justesen, Pia R. Kamstrup, Stavroula Kanoni, Fredrik Karpe, Frank Kee, Amit V. Khera, Derek Klarin, Heikki A. Koistinen, Jaspal S. Kooner, Charles Kooperberg, Kari Kuulasmaa, Johanna Kuusisto and 129 more - Nature Genetics 2017 cited by 595

  20. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Santhi K. Ganesh, Misa Graff, Namrata Gupta, Jiang He, Susan R. Heckbert, Bertha Hidalgo, Chani J. Hodonsky, Marguerite R. Irvin, Andrew D. Johnson, Eric Jorgenson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Charles Kooperberg, Jessica Lasky‐Su, Ruth J. F. Loos, Steven A. Lubitz, Rasika A. Mathias, Caitlin McHugh, Courtney G. Montgomery, Jee‐Young Moon, Alanna C. Morrison, Nicholette D. Palmer, Nathan Pankratz, George Papanicolaou, Juan M. Peralta, Patricia A. Peyser, Stephen S. Rich, Jerome I. Rotter, Edwin K. Silverman, Jennifer A. Smith, Nicholas L. Smith, Kent D. Taylor, Timothy A. Thornton, Hemant K. Tiwari, Russell P. Tracy, Tao Wang, Scott T. Weiss, Lu‐Chen Weng, Kerri L. Wiggins, James G. Wilson, Lisa R. Yanek, Sebastian Zöllner, Kari E. North, Paul L. Auer, TOPMed Hematology & Hemostasis Working Group, Laura M. Raffield, Alex P. Reiner, Yun Li - PLoS Genetics 2019 cited by 322

  21. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xiuqing Guo, Rita R. Kalyani, Charles Kooperberg, Brian G. Kral, Leslie A. Lange, Bridget M. Lin, Ani Manichaikul, Alisa K. Manning, Lisa W. Martin, Rasika A. Mathias, James B. Meigs, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Nicholette D. Palmer, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Alex P. Reiner, Muagututi‘a Sefuiva Reupena, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Kent D. Taylor, Margaret A. Taub, Ramachandran S. Vasan, Daniel E. Weeks, James G. Wilson, Lisa R. Yanek, Wei Zhao, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Nathan R. Blue, Russell P. Bowler, Ulrich Broeckel, Jai Broome, Deborah Brown and 413 more - Nature Methods 2022 cited by 109

  22. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Megan L. Grove, Albert V. Smith, Shih‐Jen Hwang, Han Chen, Tianxiao Huan, Gülüm Kosova, Nathan O. Stitziel, Sekar Kathiresan, Nilesh J. Samani, Heribert Schunkert, Panos Deloukas, Man Li, Christian Fuchsberger, Cristian Pattaro, Mathias Gorski, Charles Kooperberg, George Papanicolaou, Jacques E. Rossouw, Jessica D. Faul, Sharon L. R. Kardia, Claude Bouchard, Leslie J. Raffel, André G. Uitterlinden, Oscar H. Franco, Ramachandran S. Vasan, Christopher J. O’Donnell, Kent D. Taylor, Kiang Liu, Erwin P. Böttinger, Omri Gottesman, E. Warwick Daw, Franco Giulianini, Santhi K. Ganesh, Elias Salfati, Tamara B. Harris, Lenore J. Launer, Marcus Dörr, Stephan B. Felix, Rainer Rettig, Henry Völzke, Eric H. Kim, Wen‐Jane Lee, I‐Te Lee, Wayne H-H Sheu, Krystal S. Tsosie, Digna R. Velez Edwards, Ching‐Ti Liu, Adolfo Correa, David R. Weir, Uwe Völker, Paul M. Ridker, Eric Boerwinkle, Vilmundur Guðnason, Alex P. Reiner, Cornelia M. van Duijn, Ingrid B. Borecki, Todd L. Edwards, Aravinda Chakravarti, Jerome I. Rotter, Bruce M. Psaty, Ruth J. F. Loos, Myriam Fornage, Georg Ehret, Christopher Newton‐Cheh, Daniel Levy, Daniel I. Chasman - Nature Genetics 2016 cited by 273

  23. Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ­Rosario ­Tumino, Tyler J. VanderWeele, Walter C. Willett, Shumin Zhang, Julie E. Buring, Federico Canzian, Susan M. Gapstur, Brian E. Henderson, David J. Hunter, Graham G. Giles, Ross L. Prentice, Regina G. Ziegler, Peter Kraft, Montserrat García‐Closas, Nilanjan Chatterjee - JAMA Oncology 2016 cited by 409

  24. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Preuß, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Nicholette D. Palmer, Patricia A. Peyser, Muagututi‘a Sefuiva Reupena, Jennifer A. Smith, Xiao Sun, Kent D. Taylor, Russell P. Tracy, Michael Y. Tsai, Zhe Wang, Yuxuan Wang, Wei Bao, John T. Wilkins, Lisa R. Yanek, Wei Zhao, Donna K. Arnett, John Blangero, Eric Boerwinkle, Donald W. Bowden, Yii‐Der Ida Chen, Adolfo Correa, L. Adrienne Cupples, Susan K. Dutcher, Patrick T. Ellinor, Myriam Fornage, Stacey Gabriel, Søren Germer, Richard A. Gibbs, Jiang He, Robert C. Kaplan, Sharon L. R. Kardia, Ryan Kim, Charles Kooperberg, Ruth J. F. Loos, Karine A. Viaud‐Martinez, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, Deborah A. Nickerson, Kari E. North, Bruce M. Psaty, Susan Redline, Alex P. Reiner, Ramachandran S. Vasan, Stephen S. Rich, Cristen J. Willer, Jerome I. Rotter, Daniel J. Rader, Xihong Lin, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas and 338 more - Nature Communications 2022 cited by 74