Kimberly F. Doheny
Active 1993–2024
- 72
- Papers
- 22,578
- Citations
- 64
- h-index
- 72
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Biochemistry, Genetics and Molecular Biology54.3%
- Medicine34.8%
- Neuroscience3.7%
- Immunology and Microbiology1.2%
- Pharmacology, Toxicology and Pharmaceutics1%
- Nursing1%
- Other4%
Topics
- Genetic Associations and Epidemiology10.3%
- Genomics and Rare Diseases3.5%
- BRCA gene mutations in cancer2.5%
- Epigenetics and DNA Methylation2.3%
- Parkinson's Disease Mechanisms and Treatments2%
- Genomic variations and chromosomal abnormalities2%
- Other77.4%
Coauthors
- Elizabeth Pugh26
- Cathy C. Laurie13
- Kurt N. Hetrick11
- Hua Ling9
- Daniel B. Mirel7
- Laura J. Bierut7
- Nara Sobreira7
- Tatiana Foroud7
- Ada Hamosh6
- Anne Jackson6
- Howard J. Edenberg6
- Justin Paschall6
- Laura J. Scott6
- Peter S. Chines6
- Shalini N. Jhangiani6
- Alexandre R. Vieira5
- David R. Crosslin5
- David Valle5
- Demetrius Albanes5
- Eleanor Feingold5
- Eric Boerwinkle5
- Gail P. Jarvik5
- Heather M. Stringham5
- Joe Dennis5
All papers
- Genomic data in the All of Us Research Program
Authors: Manuscript Writing Group, Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura, Robert J. Carroll, Anjene Musick, Jodell E. Linder, I. King Jordan, Shashwat Deepali Nagar, Shivam Sharma, Robert Meller, Melissa Basford, Eric Boerwinkle, Mine Cicek, Kimberly F. Doheny, Evan E. Eichler, Stacey Gabriel, Richard A. Gibbs, David Glazer, Paul A. Harris, Gail P. Jarvik, Anthony Philippakis, Heidi L. Rehm, Dan M. Roden, Stephen N. Thibodeau, Scott Topper, Biobank, Mayo, Ashley L. Blegen, Samantha J. Wirkus, Victoria A. Wagner, Jeffrey G. Meyer, Mine Cicek, Donna M. Muzny, Eric Venner, Michelle Mawhinney, Sean Griffith, Elvin Hsu, Hua Ling, Marcia K. Adams, Kimberly Walker, Taobo Hu, HarshaVardhan Doddapaneni, Christie Kovar, Mullai Murugan, Shannon Dugan, Ziad Khan, Eric Boerwinkle, Niall J. Lennon, Christina Austin‐Tse, Eric Banks, Michael Gatzen, Namrata Gupta, Emma Henricks, Katie Larsson, Sheli McDonough, Steven M. Harrison, Christopher Kachulis, Matthew S. Lebo, Cynthia L. Neben, Marcie Steeves, Alicia Y. Zhou, Joshua D. Smith, Christian D. Frazar, Colleen Davis, Karynne Patterson, Marsha M. Wheeler, Sean McGee, Christina M. Lockwood, Brian H. Shirts, Colin C. Pritchard, Mitzi L. Murray, Valeria Vasta, Dru F. Leistritz, M Richardson, Jillian G. Buchan, Aparna Radhakrishnan, Niklas Krumm, Brenna Ehmen, Sophie Schwartz, M. Morgan T. Aster, Kristian Cibulskis, Andrea Haessly, Rebecca Asch, Aurora Cremer, Kylee Degatano, Akum Shergill, Laura D. Gauthier, Samuel K. Lee, Aaron Hatcher, George Grant, Genevieve R. Brandt, Miguel Covarrubias, Eric Banks, Ashley Able, Ashley E. Green, Robert J. Carroll, Jennifer Zhang, Henry Robert Condon and 15 more - Nature 2024 cited by 795
- Genetic analyses of diverse populations improves discovery for complex traits
Authors: Genevieve L. Wojcik, Mariaelisa Graff, Katherine K. Nishimura, Ran Tao, Jeffrey Haessler, Christopher R. Gignoux, Heather M. Highland, Yesha Patel, Elena P. Sorokin, Christy L. Avery, Gillian M. Belbin, Stephanie A. Bien, Iona Cheng, Sinéad Cullina, Chani J. Hodonsky, Yao Hu, Laura M. Huckins, Janina M. Jeff, Anne E. Justice, Jonathan Kocarnik, Unhee Lim, Bridget M. Lin, Yingchang Lu, Sarah C. Nelson, Sung-Shim L. Park, Hannah Poisner, Michael Preuß, Melissa A. Richard, Claudia Schurmann, Veronica Wendy Setiawan, Alexandra Sockell, Karan Vahi, Marie Verbanck, Abhishek Vishnu, Ryan W. Walker, Kristin L. Young, Niha Zubair, Victor Acuña-Alonso, José Luis Ambite, Kathleen C. Barnes, Eric Boerwinkle, Erwin P. Böttinger, Carlos D. Bustamante, Christian Caberto, Samuel Canizales‐Quinteros, Matthew P. Conomos, Ewa Deelman, Ron Do, Kimberly F. Doheny, Lindsay Fernández‐Rhodes, Myriam Fornage, Benyam Hailu, Gerardo Heiss, Brenna M. Henn, Lucia A. Hindorff, Rebecca D. Jackson, Cecelia Laurie, Cathy C. Laurie, Yuqing Li, Dan-Yu Lin, Andrés Moreno‐Estrada, Girish N. Nadkarni, Paul J. Norman, Loreall Pooler, Alex P. Reiner, Jane Romm, Chiara Sabatti, Karla Sandoval, Xin Sheng, Eli A. Stahl, Daniel O. Stram, Timothy A. Thornton, Christina L. Wassel, Lynne R. Wilkens, Cheryl A. Winkler, Sachi Yoneyama, Steven Buyske, Christopher A. Haiman, Charles Kooperberg, Loı̈c Le Marchand, Ruth J. F. Loos, Tara C. Matise, Kari E. North, Ulrike Peters, Eimear E. Kenny, Christopher S. Carlson - Nature 2019 cited by 1,151
- Association analysis identifies 65 new breast cancer risk loci
Authors: Kyriaki Michailidou, Sara Lindström, Joe Dennis, Jonathan Beesley, Shirley Hui, Siddhartha Kar, Audrey Lemaçon, Penny Soucy, Dylan M. Glubb, Asha Rostamianfar, Manjeet K. Bolla, Qin Wang, Jonathan P. Tyrer, Ed Dicks, Andrew Lee, Zhaoming Wang, Jamie Allen, Renske Keeman, Ursula Eilber, Juliet D. French, Xiao Qing Chen, Laura Fachal, Karen McCue, Amy E. McCart Reed, Maya Ghoussaini, Jason S. Carroll, Xia Jiang, Hilary K. Finucane, Marcia Adams, Muriel A. Adank, 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, Ãngel 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
- Discovery of common and rare genetic risk variants for colorectal cancer
Authors: Jeroen R. Huyghe, Stephanie A. Bien, Tabitha A. Harrison, Hyun Min Kang, Sai Chen, Stephanie L. Schmit, David V. Conti, Conghui Qu, Jihyoun Jeon, Christopher K. Edlund, Peyton Greenside, Michael Wainberg, Fredrick R. Schumacher, Joshua D. Smith, David Levine, Sarah C. Nelson, Nasa Sinnott-Armstrong, Demetrius Albanes, M. Henar Alonso, Kristin E. Anderson, Coral Arnau‐Collell, Volker Arndt, Christina Bamia, Barbara L. Banbury, John A. Baron, Sonja I. Berndt, Stéphane Bezieau, D. Timothy Bishop, Juergen Boehm, Heiner Boeing, Hermann Brenner, Stefanie Brezina, Stephan Buch, Daniel D. Buchanan, Andrea N. Burnett‐Hartman, Katja Butterbach, Bette J. Caan, Peter T. Campbell, Christopher S. Carlson, Sergi Castellvı́-Bel, Andrew T. Chan, Jenny Chang-Claude, Stephen J. Chanock, María‐Dolores Chirlaque, Sang‐Hee Cho, Charles M. Connolly, Amanda J. Cross, Katarina Ćuk, Keith R. Curtis, Albert de la Chapelle, Kimberly F. Doheny, David Duggan, Douglas F. Easton, Sjoerd G. Elias, Faye Elliott, Dallas R. English, Edith J. M. Feskens, Jane C. Figueiredo, Rocky Fischer, Liesel M. FitzGerald, David Forman, Manish Gala, Steven Gallinger, W. James Gauderman, Graham G. Giles, Elizabeth M. Gillanders, Jian Gong, Phyllis J. Goodman, William M. Grady, John Grove, Andrea Gsur, Marc J. Gunter, Robert W. Haile, Jochen Hampe, Heather Hampel, Sophia Harlid, Richard B. Hayes, Philipp Hofer, Michael Hoffmeister, John L. Hopper, Wan‐Ling Hsu, Wen‐Yi Huang, Thomas J. Hudson, David J. Hunter, Gemma Ibáñez‐Sanz, Gregory Idos, Roxann Ingersoll, Rebecca D. Jackson, Eric J. Jacobs, Mark A. Jenkins, Amit D. Joshi, Corinne E. Joshu, Temitope O. Keku, Timothy J. Key, Hyeong Rok Kim, Emiko Kobayashi, Laurence N. Kolonel, Charles Kooperberg, Tilman Kühn, Sébastien Küry and 99 more - Nature Genetics 2018 cited by 605
- Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Authors: Catherine M. Phelan, Karoline Kuchenbaecker, Jonathan P. Tyrer, Siddhartha Kar, Kate Lawrenson, Stacey J. Winham, Joe Dennis, Ailith Pirie, Marjorie J. Riggan, Ganna Chornokur, Madalene A. Earp, Paulo C. Lyra, Janet M. Lee, Simon G. Coetzee, Jonathan Beesley, Lesley McGuffog, Penny Soucy, Ed Dicks, Andrew Lee, Daniel Barrowdale, Julie Lecarpentier, Goska Leslie, Cora M. Aalfs, Katja K.H. Aben, Marcia Adams, Julian Adlard, Irene L. Andrulis, Hoda Anton‐Culver, Natalia Antonenkova, AOCS study group, Gerasimos Aravantinos, Norbert Arnold, Banu Arun, Brita Arver, Jacopo Azzollini, Judith Balmañà, Susana Banerjee, Laure Barjhoux, Rósa B. Barkardóttir, Yukie T. Bean, Matthias W Beckmann, Alicia Beeghly-Fadiel, Javier Benı́tez, Marina Bermisheva, Marcus Q. Bernardini, Michael J. Birrer, Line Bjorge, Amanda Black, Kenneth B. Blankstein, Marinus J. Blok, Clara Bodelón, Natalia Bogdanova, Anders Bojesen, Bernardo Bonanni, Åke Borg, Angela R. Bradbury, James D. Brenton, Carole Brewer, Louise A. Brinton, Per Broberg, Angela Brooks‐Wilson, Fiona Bruinsma, Joan Brunet, Bruno Buecher, Ralf Butzow, Saundra S. Buys, Trinidad Caldés, Maria A. Caligo, Ian Campbell, Rikki Cannioto, Michael E. Carney, Terence Cescon, Salina B Chan, Jenny Chang-Claude, Stephen J. Chanock, Xiao Qing Chen, Yoke-Eng Chiew, Jocelyne Chiquette, Wendy K. Chung, Kathleen Claes, Thomas Conner, Linda S. Cook, Jackie Cook, Daniel W. Cramer, Julie M. Cunningham, Aimee A. D’Aloisio, Mary B Daly, Francesca Damiola, Sakaeva Dina Damirovna, Agnieszka Dansonka‐Mieszkowska, Fanny Dao, Rosemarie Davidson, Anna DeFazio, Capucine Delnatte, Kimberly F. Doheny, Orland Dı́ez, Yuan Chun Ding, Jennifer A. Doherty, Susan M. Domchek, Cecilia M. Dorfling and 320 more - Nature Genetics 2017 cited by 553
- Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data
Authors: Goo Jun, Matthew Flickinger, Kurt N. Hetrick, Jane Romm, Kimberly F. Doheny, Gonçalo R. Abecasis, Michael Boehnke, Hyun Min Kang - The American Journal of Human Genetics 2012 cited by 551
- Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
Authors: Taye H. Hamza, Cyrus P. Zabetian, Albert Tenesa, Alain Laederach, Jennifer S. Montimurro, Dora Yearout, Denise M. Kay, Kimberly F. Doheny, Justin Paschall, Elizabeth Pugh, Victoria I. Kusel, Randall V. Collura, John W. Roberts, Alida Griffith, Ali Samii, William K. Scott, John G. Nutt, Stewart A. Factor, Haydeh Payami - Nature Genetics 2010 cited by 814
- A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants
Authors: Laura J. Scott, Karen L. Mohlke, Lori L. Bonnycastle, Cristen J. Willer, Yun Li, William L. Duren, Michael R. Erdos, Heather M. Stringham, Peter S. Chines, Anne Jackson, Ludmila Prokunina‐Olsson, Chia-Jen Ding, Amy J. Swift, Narisu Narisu, Tianle Hu, Randall Pruim, Rui Xiao, Xiaoyi Li, Karen N. Conneely, Nancy L. Riebow, Andrew G. Sprau, Maurine Tong, Peggy P. White, Kurt N. Hetrick, Michael W. Barnhart, Craig W. Bark, Janet L. Goldstein, Lee Watkins, Xiang Fang, Jouko Saramies, Thomas A. Buchanan, Richard M. Watanabe, Timo T. Valle, Leena Kinnunen, Gonçalo R. Abecasis, Elizabeth Pugh, Kimberly F. Doheny, Richard N. Bergman, Jaakko Tuomilehto, Francis S. Collins, Michael Boehnke - Science 2007 cited by 2,781
- Detectable clonal mosaicism from birth to old age and its relationship to cancer
Authors: Cathy C. Laurie, Cecelia Laurie, Kenneth Rice, Kimberly F. Doheny, Leila R. Zelnick, Caitlin McHugh, Hua Ling, Kurt N. Hetrick, Elizabeth Pugh, Chris Amos, Qingyi Wei, Lie Wang, Jeffrey E. Lee, Kathleen C. Barnes, Nadia N. Hansel, Rasika A. Mathias, Denise Daley, Terri H. Beaty, Alan F. Scott, Ingo Ruczinski, Rob Scharpf, Laura J. Bierut, Sarah M. Hartz, Maria Teresa Landi, Neal D. Freedman, Lynn R. Goldin, David Ginsburg, Jun Li, Karl C. Desch, Sara S. Strom, William J. Blot, Lisa B. Signorello, Sue A. Ingles, Stephen J. Chanock, Sonja I. Berndt, Loı̈c Le Marchand, Brian E. Henderson, Kristine R. Monroe, John A. Heit, Mariza de Andrade, Sebastian M. Armasu, C Régnier, William L. Lowe, M. Geoffrey Hayes, Mary L. Marazita, Eleanor Feingold, Jeffrey C. Murray, Mads Melbye, Bjarke Feenstra, Jae H. Kang, Janey L. Wiggs, Gail P. Jarvik, Andrew McDavid, Venkatraman Seshan, Daniel B. Mirel, Andrew Crenshaw, Nataliya Sharopova, Anastasia L. Wise, Jess Shen, David R. Crosslin, David Levine, Xiuwen Zheng, Jenna Udren, Siiri Bennett, Sarah C. Nelson, Stephanie M. Gogarten, Matthew P. Conomos, Patrick J. Heagerty, Teri A. Manolio, Louis R. Pasquale, Christopher A. Haiman, Neil E. Caporaso, Bruce S. Weir - Nature Genetics 2012 cited by 599
- The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
Authors: Jessica X. Chong, Kati J. Buckingham, Shalini N. Jhangiani, Corinne D. Boehm, Nara Sobreira, Joshua D. Smith, Tanya M. Harrell, Margaret J. McMillin, Wojciech Wiszniewski, Tomasz Gambin, Zeynep H. Coban Akdemir, Kimberly F. Doheny, Alan F. Scott, Dimitri Avramopoulos, Aravinda Chakravarti, Julie Hoover‐Fong, Debra Mathews, P. Dane Witmer, Hua Ling, Kurt N. Hetrick, Lee Watkins, Karynne Patterson, Frédéric Reinier, Elizabeth Blue, Donna M. Muzny, Martin Kircher, Kaya Bilgüvar, Francesc López‐Giráldez, V. Reid Sutton, Holly K. Tabor, Suzanne M. Leal, Murat Günel, Shrikant Mane, Richard A. Gibbs, Eric Boerwinkle, Ada Hamosh, Jay Shendure, James R. Lupski, Richard P. Lifton, David Valle, Deborah A. Nickerson, Michael J. Bamshad - The American Journal of Human Genetics 2015 cited by 688
- Quality control and quality assurance in genotypic data for genome‐wide association studies
Authors: Cathy C. Laurie, Kimberly F. Doheny, Daniel B. Mirel, Elizabeth Pugh, Laura J. Bierut, Tushar Bhangale, Frederick J. Boehm, Neil E. Caporaso, Marilyn C. Cornelis, Howard J. Edenberg, Stacy Gabriel, Emily Harris, Frank B. Hu, Kevin B. Jacobs, Peter Kraft, Maria Teresa Landi, Thomas Lumley, Teri A. Manolio, Caitlin McHugh, Ian Painter, Justin Paschall, John P. Rice, Kenneth Rice, Xiuwen Zheng, Bruce S. Weir, for the GENEVA Investigators - Genetic Epidemiology 2010 cited by 498
- Quality Control Procedures for Genome‐Wide Association Studies
Authors: Stephen Turner, Loren L. Armstrong, Yuki Bradford, Christopher S. Carlson, Dana C. Crawford, Andrew Crenshaw, Mariza de Andrade, Kimberly F. Doheny, Jonathan L. Haines, Geoffrey Hayes, Gail P. Jarvik, Lan Jiang, Iftikhar J. Kullo, Rongling Li, Hua Ling, Teri A. Manolio, Martha Matsumoto, Catherine A. McCarty, Andrew McDavid, Daniel B. Mirel, Justin Paschall, Elizabeth Pugh, Luke V. Rasmussen, Russell A. Wilke, Rebecca L. Zuvich, Marylyn D. Ritchie - Current Protocols in Human Genetics 2011 cited by 378
- Centers for Mendelian Genomics: A decade of facilitating gene discovery
Authors: Samantha Baxter, Jennifer E. Posey, Nicole J. Lake, Nara Sobreira, Jessica X. Chong, Steven Buyske, Elizabeth Blue, Lisa H. Chadwick, Zeynep Coban‐Akdemir, Kimberly F. Doheny, Colleen Davis, Monkol Lek, Christopher Wellington, Shalini N. Jhangiani, Mark Gerstein, Richard A. Gibbs, Richard P. Lifton, Daniel G. MacArthur, Tara C. Matise, James R. Lupski, David Valle, Michael J. Bamshad, Ada Hamosh, Shrikant Mane, Deborah A. Nickerson, Marcia Adams, François Aguet, Gülsen Akay, Peter Anderson, Corina Antonescu, Harindra Arachchi, Mehmed M. Atik, Christina Austin‐Tse, Larry Babb, Tamara Bacus, Vahid Bahrambeigi, Suganthi Balasubramanian, Yavuz Bayram, Arthur L. Beaudet, Christine R. Beck, John W. Belmont, Jennifer E. Below, Kaya Bilgüvar, Corinne D. Boehm, Eric Boerwinkle, Philip M. Boone, Sara J. Bowne, Harrison Brand, Kati J. Buckingham, Alicia B. Byrne, Daniel G. Calame, Ian M. Campbell, Xiaolong Cao, Claudia M.B. Carvalho, Varuna Chander, Jaime Chang, Katherine R. Chao, Iván K. Chinn, Declan Clarke, Ryan L. Collins, Beryl B. Cummings, Zain Dardas, Moez Dawood, Kayla Delano, Stephanie DiTroia, HarshaVardhan Doddapaneni, Haowei Du, Renqian Du, Ruizhi Duan, Mohammad K. Eldomery, Christine M. Eng, Eleina England, Emily Evangelista, Selin Everett, Jawid M. Fatih, Adam L. Felsenfeld, Laurent C. Francioli, Christian D. Frazar, Jack Fu, Emmanuel Gamarra, Tomasz Gambin, Weiniu Gan, Mira Gandhi, Vijay Ganesh, Kiran Garimella, Laura D. Gauthier, Danielle Giroux, Claudia Gonzaga‐Jauregui, Julia K. Goodrich, William W. Gordon, Sean Griffith, Christopher M. Grochowski, Shen Gu, Sanna Gudmundsson, Stacey Hall, Adam Hansen, Tamar Harel, Arif Harmanci, Isabella Herman, Kurt N. Hetrick and 142 more - Genetics in Medicine 2022 cited by 80
- A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Authors: NBCS Collaborators, Lang Wu, kConFab/AOCS Investigators, Wei Shi, Jirong Long, Xingyi Guo, Kyriaki Michailidou, Jonathan Beesley, Manjeet K. Bolla, Xiao‐Ou Shu, Yingchang Lu, Qiuyin Cai, Fares Al‐Ejeh, Esdy Rozali, Qin Wang, Joe Dennis, Bingshan Li, Chenjie Zeng, Helian Feng, Alexander Gusev, Richard Barfield, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Kristan J. Aronson, Paul L. Auer, Myrto Barrdahl, Caroline Baynes, Matthias W. Beckmann, Javier Benı́tez, Marina Bermisheva, Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Hiltrud Brauch, Hermann Brenner, Louise A. Brinton, Per Broberg, Sara Y. Brucker, Barbara Burwinkel, Trinidad Caldés, Federico Canzian, Brian D. Carter, Jose E. Castelao, Jenny Chang‐Claude, Xiaoqing Chen, Ting‐Yuan David Cheng, Hans Christiansen, Christine L. Clarke, Margriet Collée, Sten Cornelissen, Fergus J. Couch, 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, Miriam Dwek, Diana M. Eccles, Ursula Eilber, A. Heather Eliassen, Christoph Engel, Mikael Eriksson, Laura Fachal, Peter A. Fasching, Jonine D. Figueroa, Dieter Flesch‐Janys, Olivia Fletcher, Henrik Flyger, Lin Fritschi, Marike Gabrielson, Manuela Gago-Domínguez, Susan M. Gapstur, Montserrat García‐Closas, Mia M. Gaudet, Maya Ghoussaini, Graham G. Giles, Mark S. Goldberg, David E. Goldgar, Anna González‐Neira, Pascal Guénel, Eric Hahnen, Christopher A. Haiman, Niclas Håkansson, Per Hall, Emily Hallberg, Ute Hamann, Patricia Harrington, Alexander Hein, Belynda Hicks, Peter Hillemanns, Antoinette Hollestelle, Robert N. Hoover, John L. Hopper and 112 more - Nature Genetics 2018 cited by 246
- Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
Authors: Wei Chen, Dwight Stambolian, Albert O. Edwards, Kari Branham, Mohammad Othman, Jóhanna Jakobsdóttir, Nirubol Tosakulwong, Margaret A. Pericak‐Vance, Peter A. Campochiaro, Michael L. Klein, Perciliz L. Tan, Yvette P. Conley, Atsuhiro Kanda, Laura J. Kopplin, Yanming Li, Katherine J. Augustaitis, Athanasios J. Karoukis, William K. Scott, Anita Agarwal, Jaclyn L. Kovach, Stephen G. Schwartz, Eric A. Postel, Matthew Brooks, Keith H. Baratz, William L. Brown, Alexander J. Brucker, Anton Orlin, Gary C. Brown, Allen C. Ho, Carl D. Regillo, Larry A. Donoso, Lifeng Tian, Brian Kaderli, Dexter Hadley, Stephanie A. Hagstrom, Neal S. Peachey, Ronald Klein, Barbara E.K. Klein, Norimoto Gotoh, Kenji Yamashiro, Frederick L. Ferris, Jesen Fagerness, Robyn Reynolds, Lindsay A. Farrer, Ivana K. Kim, Joan W. Miller, Marta Cortón, Ãngel Carracedo, Manuel Sánchez‐Salorio, Elizabeth Pugh, Kimberly F. Doheny, Marı́a Brión, Margaret M. DeAngelis, Daniel E. Weeks, Donald J. Zack, Emily Y. Chew, John R. Heckenlively, Nagahisa Yoshimura, Sudha K. Iyengar, Peter J. Francis, Nicholas Katsanis, Johanna M. Seddon, Jonathan L. Haines, Michael B. Gorin, Gonçalo R. Abecasis, Anand Swaroop, Robert N. Johnson, Everett Ai, H. Richard McDonald, Margaret Stolarczuk, Peter R. Pavan, Karina K. Billiris, Mohan Iyer, Matthew M. Menosky, Scott E. Pautler, Sharon M. Millard, G. Baker Hubbard, Thomas Aaberg, Lindy DuBois, Alice T. Lyon, Susan Anderson-Nelson, Lee M. Jampol, David V. Weinberg, Annie Muñana, Zuzanna Rozenbajgier, David H. Orth, Jack Cohen, Matthew MacCumber, Matthew MacCumber, Celeste Figliulo, Liz Porcz, James C. Folk, H. Culver Boldt, Stephen R. Russell, Rachel Ivins, Connie J. Hinz, Charles C. Barr, Steve Bloom, Ken Jaegers, Brian Kritchman and 68 more - National Academy of Sciences, Proceedings of the National Academy of Sciences 2010 cited by 516
- The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers
Authors: Christopher I. Amos, Joe Dennis, Zhaoming Wang, Jinyoung Byun, Fredrick R. Schumacher, Simon A. Gayther, Graham Casey, David J. Hunter, Thomas A. Sellers, Stephen B. Gruber, Alison M. Dunning, Kyriaki Michailidou, Laura Fachal, Kimberly F. Doheny, Amanda B. Spurdle, Yafang Li, Xiangjun Xiao, Jane Romm, Elizabeth Pugh, Gerhard A. Coetzee, Dennis J. Hazelett, Stig E. Bojesen, Charlisse Caga-Anan, Christopher A. Haiman, Ahsan Kamal, Craig Luccarini, Daniel C. Tessier, Daniel Vincent, François Bacot, David Van Den Berg, Stefanie A. Nelson, Stephen Demetriades, David E. Goldgar, Fergus J. Couch, Judith L. Forman, Graham G. Giles, David V. Conti, Heike Bickeböller, Angela Risch, Mélanie Waldenberger, Irene Brüske‐Hohlfeld, Belynda Hicks, Hua Ling, Lesley McGuffog, Andrew Lee, Karoline Kuchenbaecker, Penny Soucy, Judith Manz, Julie M. Cunningham, Katja Butterbach, Zsofia Kote‐Jarai, Peter Kraft, Liesel M. FitzGerald, Sara Lindström, Marcia Adams, James McKay, Catherine M. Phelan, Sara Benlloch, Linda E. Kelemen, Paul Brennan, Marjorie J. Riggan, Tracy A. O’Mara, Hongbing Shen, Yongyong Shi, Deborah J. Thompson, Marc T. Goodman, Sune F. Nielsen, Andrew Berchuck, Sylvie LaBoissière, Stephanie L. Schmit, Tameka Shelford, Christopher K. Edlund, Jack A. Taylor, John K. Field, Sue K. Park, Kenneth Offit, Mads Thomassen, Rita K. Schmutzler, Laura Ottini, Rayjean J. Hung, Jonathan Marchini, Ali Amin Al Olama, Ulrike Peters, Rosalind A. Eeles, Michael F. Seldin, Elizabeth M. Gillanders, Daniela Seminara, Antonis C. Antoniou, Paul D.P. Pharoah, Georgia Chenevix‐Trench, Stephen J. Chanock, Jacques Simard, Douglas F. Easton - Cancer Epidemiology Biomarkers & Prevention 2016 cited by 393
- Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer
Authors: Burcu F. Darst, Edward J. Saunders, Tokhir Dadaev, Xin Sheng, Peggy Wan, Loreall Pooler, Lucy Xia, Stephen Chanock, Sonja I. Berndt, Ying Wang, Alpa V. Patel, Demetrius Albanes, Stephanie J. Weinstein, Vincent J. Gnanapragasam, Chad D. Huff, Fergus J. Couch, Alicja Wolk, Graham G. Giles, Tú Nguyen‐Dumont, Roger L. Milne, Mark M. Pomerantz, Julie A. Schmidt, Ruth C. Travis, Timothy J. Key, Konrad H. Stopsack, Lorelei A. Mucci, William J. Catàlona, Beth Marosy, Kurt N. Hetrick, Kimberly F. Doheny, Robert J. MacInnis, Melissa C. Southey, Rosalind A. Eeles, Fredrik Wiklund, David V. Conti, Zsofia Kote‐Jarai, Christopher A. Haiman - JAMA Oncology 2023 cited by 51
- Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
Authors: Eric Venner, Donna M. Muzny, Joshua D. Smith, Kimberly Walker, Cynthia L. Neben, Christina M. Lockwood, Phillip E. Empey, Ginger Metcalf, Chris Kachulis, Sana Mian, Anjene Musick, Heidi L. Rehm, Steven M. Harrison, Stacey Gabriel, Richard A. Gibbs, Deborah A. Nickerson, Alicia Y. Zhou, Kimberly F. Doheny, Bradley A. Ozenberger, Scott Topper, Niall J. Lennon - Genome Medicine 2022 cited by 63
- Genome‐Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry
Authors: Kimberly E. Taylor, Quenna Wong, David Levine, Caitlin McHugh, Cathy C. Laurie, Kimberly F. Doheny, Mi Y. Lam, Alan N. Baer, Stephen Challacombe, Héctor Lanfranchi, Morten Schiødt, Muthiah Srinivasan, Hisanori Umehara, Frederick B. Vivino, Yan Zhao, Stephen Shiboski, Troy E. Daniels, John S. Greenspan, Caroline H. Shiboski, Lindsey A. Criswell - Arthritis & Rheumatology 2017 cited by 131
- Genomewide association study for susceptibility genes contributing to familial Parkinson disease
Authors: Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle, Anita L. DeStefano, Cheryl Halter, Elizabeth Pugh, Kimberly F. Doheny, James F. Gusella, William C. Nichols, Tatiana Foroud, Richard H. Myers, The PSG—PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories - Human Genetics 2008 cited by 444
- Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2
Authors: Nathan Pankratz, Gary W. Beecham, Anita L. DeStefano, Ted M. Dawson, Kimberly F. Doheny, Stewart A. Factor, Taye H. Hamza, Albert Y. Hung, Bradley T. Hyman, Adrian J. Ivinson, Dmitri Krainc, Jeanne C. Latourelle, Lorraine N. Clark, Karen Marder, Eden R. Martin, Richard Mayeux, Owen A. Ross, Clemens R. Scherzer, David K. Simon, Caroline M. Tanner, Jeffery M. Vance, Zbigniew K. Wszołek, Cyrus P. Zabetian, Richard H. Myers, Haydeh Payami, William K. Scott, Tatiana Foroud - Annals of Neurology 2011 cited by 299
- Insights into genetics, human biology and disease gleaned from family based genomic studies
Authors: Jennifer E. Posey, Anne O’Donnell‐Luria, Jessica X. Chong, Tamar Harel, Shalini N. Jhangiani, Zeynep H. Coban Akdemir, Steven Buyske, Davut Pehli̇van, Claudia M.B. Carvalho, Samantha Baxter, Nara Sobreira, Pengfei Liu, Nan Wu, Jill A. Rosenfeld, Sushant Kumar, Dimitri Avramopoulos, Janson J. White, Kimberly F. Doheny, P. Dane Witmer, Corinne D. Boehm, V. Reid Sutton, Donna M. Muzny, Eric Boerwinkle, Murat Günel, Deborah A. Nickerson, Shrikant Mane, Daniel G. MacArthur, Richard A. Gibbs, Ada Hamosh, Richard P. Lifton, Tara C. Matise, Heidi L. Rehm, Mark Gerstein, Michael J. Bamshad, David Valle, James R. Lupski - Genetics in Medicine 2019 cited by 211
- Identification of HKDC1 and BACE2 as Genes Influencing Glycemic Traits During Pregnancy Through Genome-Wide Association Studies
Authors: M. Geoffrey Hayes, Margrit Urbanek, Marie‐France Hivert, Loren L. Armstrong, Jean Morrison, Cong Guo, Lynn P. Lowe, Douglas A. Scheftner, Anna Pluzhnikov, David Levine, Caitlin McHugh, C. Ackerman, Luigi Bouchard, Diane Brisson, Brian T. Layden, Daniel B. Mirel, Kimberly F. Doheny, Marysa Leya, Rachel N. Lown-Hecht, Alan R. Dyer, Boyd E. Metzger, Timothy E. Reddy, Nancy J. Cox, William L. Lowe - Diabetes 2013 cited by 154
- Variant‐level matching for diagnosis and discovery: Challenges and opportunities
Authors: Eliete da S. Rodrigues, Sean Griffith, Renan Paulo Martin, Corina Antonescu, Jennifer E. Posey, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Kimberly F. Doheny, James R. Lupski, David Valle, Michael J. Bamshad, Ada Hamosh, Assaf Sheffer, Jessica X. Chong, Yaron Einhorn, Miro Cupak, Nara Sobreira - Human Mutation 2022 cited by 44
