Daniel J. Schaid
Active 1987–2024
- 155
- Papers
- 33,853
- Citations
- 96
- h-index
- 153
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.2%
- Mayo Clinic1%
- Johns Hopkins University0.7%
- Massachusetts General Hospital0.6%
- Broad Institute0.6%
- Brigham and Women's Hospital0.5%
- Other95.4%
Fields
- Medicine46.9%
- Biochemistry, Genetics and Molecular Biology41.6%
- Immunology and Microbiology3.2%
- Neuroscience3.1%
- Pharmacology, Toxicology and Pharmaceutics1%
- Psychology0.8%
- Other3.4%
Topics
- Genetic Associations and Epidemiology5.9%
- Genetic factors in colorectal cancer5.6%
- BRCA gene mutations in cancer3.1%
- Cancer Genomics and Diagnostics2.9%
- Genomics and Rare Diseases2.8%
- Colorectal Cancer Screening and Detection2%
- Other77.7%
Coauthors
- Shannon K. McDonnell44
- Stephen N. Thibodeau39
- Julie M. Cunningham21
- Iftikhar J. Kullo15
- Scott J. Hebbring12
- Johanna Schleutker11
- Richard M. Weinshilboum11
- Brett J. Peterson9
- Gail P. Jarvik9
- Janet L. Stanford9
- Michael L. Blute9
- Ozan Dikilitas9
- Steven J. Jacobsen9
- Amy J. French8
- Graham G. Giles8
- Lynn C. Hartmann8
- Anthony Batzler7
- David E. Neal7
- Demetrius M. Maraganore7
- Fergus J. Couch7
- Lawrence J. Burgart7
- Liang Wang7
- Thomas A. Sellers7
- Walter A. Rocca7
All papers
- REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
Authors: Nilah M. Ioannidis, Joseph H. Rothstein, Vikas Pejaver, Sumit Middha, Shannon K. McDonnell, Saurabh Baheti, Anthony M. Musolf, Qing Li, Emily Holzinger, Danielle M. Karyadi, Lisa Cannon‐Albright, Craig C. Teerlink, Janet L. Stanford, William B. Isaacs, Jianfeng Xu, Kathleen A. Cooney, Ethan M. Lange, Johanna Schleutker, John D. Carpten, Isaac J. Powell, Olivier Cussenot, Géraldine Cancel‐Tassin, Graham G. Giles, Robert J. MacInnis, Christiane Maier, Chih‐Lin Hsieh, Fredrik Wiklund, William J. Catàlona, William D. Foulkes, Diptasri Mandal, Rosalind A. Eeles, Zsofia Kote‐Jarai, Carlos D. Bustamante, Daniel J. Schaid, Trevor Hastie, Elaine A. Ostrander, Joan E. Bailey‐Wilson, Predrag Radivojac, Stephen N. Thibodeau, Alice S. Whittemore, Weiva Sieh - The American Journal of Human Genetics 2016 cited by 2,986
- From genome-wide associations to candidate causal variants by statistical fine-mapping
Authors: Daniel J. Schaid, Wenan Chen, Nicholas B. Larson - Nature Reviews Genetics 2018 cited by 967
- Principles and methods for transferring polygenic risk scores across global populations
Authors: Linda Kachuri, Nilanjan Chatterjee, Jibril Hirbo, Daniel J. Schaid, Iman K. Martin, Iftikhar J. Kullo, Eimear E. Kenny, Bogdan Paşaniuc, Paul L. Auer, Matthew P. Conomos, David V. Conti, Yi Ding, Ying Wang, Haoyu Zhang, Yuji Zhang, John S. Witte, Tian Ge - Nature Reviews Genetics 2023 cited by 313
- Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations
Authors: Niall J. Lennon, Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin, Jennifer E. Below, Sonja I. Berndt, Wendy K. Chung, James J. Cimino, Ellen Wright Clayton, John J. Connolly, David R. Crosslin, Ozan Dikilitas, Digna R. Velez Edwards, QiPing Feng, Marissa Fisher, Robert R. Freimuth, Tian Ge, Sonja Berndt, Joel N. Hirschhorn, Ruth J. F. Loos, Joseph Glessner, Allan Gordon, Candace Patterson, Håkon Håkonarson, Maegan Harden, Margaret Harr, Joel N. Hirschhorn, Clive Hoggart, Li Hsu, Marguerite R. Irvin, Gail P. Jarvik, Elizabeth W. Karlson, Atlas Khan, Amit V. Khera, Krzysztof Kiryluk, Iftikhar J. Kullo, Katie Larkin, Nita A. Limdi, Jodell E. Linder, Ruth J. F. Loos, Yuan Luo, Edyta Małolepsza, Teri A. Manolio, Lisa J. Martin, L.R. McCarthy, Elizabeth M. McNally, James B. Meigs, Tesfaye B. Mersha, Jonathan D. Mosley, Anjene Musick, Bahram Namjou, Nihal Pai, Lorenzo L. Pesce, Ulrike Peters, Josh F. Peterson, Cynthia A. Prows, Megan J. Puckelwartz, Heidi L. Rehm, Dan M. Roden, Elisabeth A. Rosenthal, Robb Rowley, Konrad Teodor Sawicki, Daniel J. Schaid, Roelof A. J. Smit, Johanna L. Smith, Jordan W. Smoller, Minta Thomas, Hemant K. Tiwari, Diana M. Toledo, Nataraja Sarma Vaitinadin, David L. Veenstra, Theresa L. Walunas, Zhe Wang, Wei‐Qi Wei, Chunhua Weng, Georgia L. Wiesner, Xianyong Yin, Eimear E. Kenny - Nature Medicine 2024 cited by 189
- Genome-wide polygenic score to predict chronic kidney disease across ancestries
Authors: Atlas Khan, Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru, Alana Jones, Edyta Małolepsza, Ozan Dikilitas, Iftikhar J. Kullo, Daniel J. Schaid, Elizabeth W. Karlson, Tian Ge, James B. Meigs, Jordan W. Smoller, Christoph Lange, David R. Crosslin, Gail P. Jarvik, Pavan K. Bhatraju, Jacklyn N. Hellwege, Paulette D. Chandler, Laura Rasmussen Torvik, Alex Fedotov, Cong Liu, Christopher Kachulis, Niall J. Lennon, Noura S. Abul‐Husn, Judy H. Cho, Iuliana Ionita‐Laza, Ali G. Gharavi, Wendy K. Chung, George Hripcsak, Chunhua Weng, Girish N. Nadkarni, Marguerite R. Irvin, Hemant K. Tiwari, Eimear E. Kenny, Nita A. Limdi, Krzysztof Kiryluk - Nature Medicine 2022 cited by 162
- Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
Authors: Tian Ge, Marguerite R. Irvin, Amit Patki, Vinodh Srinivasasainagendra, Kuang Lin, Hemant K. Tiwari, Nicole D. Armstrong, Barbara Benoit, Chia‐Yen Chen, Karmel W. Choi, James J. Cimino, Brittney H. Davis, Ozan Dikilitas, Bethany Etheridge, Yen‐Chen Anne Feng, Vivian S. Gainer, Hailiang Huang, Gail P. Jarvik, Christopher Kachulis, Eimear E. Kenny, Atlas Khan, Krzysztof Kiryluk, Leah C. Kottyan, Iftikhar J. Kullo, Christoph Lange, Niall J. Lennon, Aaron Leong, Edyta Małolepsza, Ayme D. Miles, Shawn N. Murphy, Bahram Namjou, Renuka Narayan, Mark J. O’Connor, Jennifer A. Pacheco, Emma Perez, Laura J. Rasmussen‐Torvik, Elisabeth A. Rosenthal, Daniel J. Schaid, Maria Stamou, Miriam S. Udler, Wei‐Qi Wei, Scott T. Weiss, Maggie C. Y. Ng, Jordan W. Smoller, Matthew S. Lebo, James B. Meigs, Nita A. Limdi, Elizabeth W. Karlson - Genome Medicine 2022 cited by 173
- Microsatellite Instability in Cancer of the Proximal Colon
Authors: Stephen N. Thibodeau, Gary D. Bren, Daniel J. Schaid - Science 1993 cited by 3,145
- Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates
Authors: Iftikhar J. Kullo, Hayan Jouni, Erin Austin, Sherry‐Ann Brown, Teresa Kruisselbrink, Iyad Isseh, Raad A. Haddad, Tariq S. Marroush, Khader Shameer, Janet E. Olson, Ulrich Broeckel, Robert C. Green, Daniel J. Schaid, Víctor M. Montori, Kent R. Bailey - Circulation 2016 cited by 270
- Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk
Authors: Minta Thomas, Lori C. Sakoda, Michael Hoffmeister, Elisabeth A. Rosenthal, Jeffrey K. Lee, Fränzel J.B. van Duijnhoven, Elizabeth A. Platz, Anna H. Wu, Christopher H. Dampier, Albert de la Chapelle, Alicja Wolk, Amit D. Joshi, Andrea N. Burnett‐Hartman, Andrea Gsur, Annika Lindblom, Antoni Castells, Aung Ko Win, Bahram Namjou, Bethany Van Guelpen, Catherine M. Tangen, Qianchuan He, Christopher I. Li, Clemens Schafmayer, Corinne E. Joshu, Cornelia M. Ulrich, D. Timothy Bishop, Daniel D. Buchanan, Daniel J. Schaid, David A. Drew, David C. Muller, David Duggan, David R. Crosslin, Demetrius Albanes, Edward L. Giovannucci, Eric B. Larson, Flora Qu, Frank Mentch, Graham G. Giles, Håkon Håkonarson, Heather Hampel, Ian B. Stanaway, Jane C. Figueiredo, Jeroen R. Huyghe, Jessica Minnier, Jenny Chang‐Claude, Jochen Hampe, John B. Harley, Kala Visvanathan, Keith R. Curtis, Kenneth Offit, Li Li, Loı̈c Le Marchand, Ludmila Vodičková, Marc J. Gunter, Mark A. Jenkins, Martha L. Slattery, Mathieu Lemire, Michael O. Woods, Mingyang Song, Neil Murphy, Noralane M. Lindor, Ozan Dikilitas, Paul D.P. Pharoah, Peter T. Campbell, Polly A. Newcomb, Roger L. Milne, Robert J. MacInnis, Sergi Castellvı́-Bel, Shuji Ogino, Sonja I. Berndt, Stéphane Bezieau, Stephen N. Thibodeau, Steven Gallinger, Syed Hassan Ejaz Zaidi, Tabitha A. Harrison, Temitope O. Keku, Thomas J. Hudson, Veronika Vymetálková, Vı́ctor Moreno, Vicente Martín, Volker Arndt, Wei‐Qi Wei, Wendy K. Chung, Yu‐Ru Su, Richard B. Hayes, Emily White, Pavel Vodička, Graham Casey, Stephen B. Gruber, Robert E. Schoen, Andrew T. Chan, John D. Potter, Hermann Brenner, Gail P. Jarvik, Douglas A. Corley, Ulrike Peters, Li Hsu - The American Journal of Human Genetics 2020 cited by 228
- Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics
Authors: Wenan Chen, Beth R. Larrabee, Inna G. Ovsyannikova, Richard B. Kennedy, Iana H. Haralambieva, Gregory A. Poland, Daniel J. Schaid - Genetics 2015 cited by 261
- Risk tables for parkinsonism and Parkinson's disease
Authors: Alexis Elbaz, James H. Bower, Demetrius M. Maraganore, Shannon K. McDonnell, Brett J. Peterson, J. Eric Ahlskog, Daniel J. Schaid, Walter A. Rocca - Journal of Clinical Epidemiology 2002 cited by 376
- Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups
Authors: Ozan Dikilitas, Daniel J. Schaid, Matthew Kosel, Robert J. Carroll, Christopher G. Chute, Joshua C. Denny, Alex Fedotov, QiPing Feng, Håkon Håkonarson, Gail P. Jarvik, Ming Ta Michael Lee, Jennifer A. Pacheco, Robb Rowley, Patrick Sleiman, Christoph Stein, Amy C. Sturm, Wei‐Qi Wei, Georgia L. Wiesner, Marc S. Williams, Yanfei Zhang, Teri A. Manolio, Iftikhar J. Kullo - The American Journal of Human Genetics 2020 cited by 173
- Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
Authors: Siddhartha Kar, Jonathan Beesley, Ali Amin Al Olama, Kyriaki Michailidou, Jonathan P. Tyrer, Zsofia Kote‐Jarai, Kate Lawrenson, Sara Lindström, Susan J. Ramus, Deborah J. Thompson, ABCTB Investigators, Adam S. Kibel, Agnieszka Dansonka‐Mieszkowska, Agnieszka Michael, Aida Karina Dieffenbach, Aleksandra Gentry‐Maharaj, Alice S. Whittemore, Alicja Wolk, Álvaro N.A. Monteiro, Ana Peixoto, Andrzej Kierzek, Angela Cox, Anja Rudolph, Anna González‐Neira, Anna H. Wu, Annika Lindblom, Anthony J. Swerdlow, AOCS Study Group & Australian Cancer Study (Ovarian Cancer), APCB BioResource, Argyrios Ziogas, Arif B. Ekici, Barbara Burwinkel, Beth Y. Karlan, Børge G. Nordestgaard, Carl Blomqvist, Catherine Phelan, Catriona McLean, Celeste Leigh Pearce, Celine M. Vachon, Cezary Cybulski, Chavdar Slavov, Christa Stegmaier, Christiane Maier, Christine B. Ambrosone, Claus Høgdall, Craig C. Teerlink, Daehee Kang, Daniel C. Tessier, Daniel J. Schaid, Daniel O. Stram, Daniel W. Cramer, David E. Neal, Diana Eccles, Dieter Flesch‐Janys, Digna R. Velez Edwards, Dominika Wokozorczyk, Douglas A. Levine, Drakoulis Yannoukakos, Elinor J. Sawyer, Elisa V. Bandera, Elizabeth M. Poole, Ellen L. Goode, Э. К. Хуснутдинова, Estrid Høgdall, Fengju Song, Fiona Bruinsma, Florian Heitz, Francesmary Modugno, Freddie C. Hamdy, Fredrik Wiklund, Graham G. Giles, Håkan Olsson, Hans Wildiers, Hans-Ulrich Ulmer, Hardev Pandha, Harvey A. Risch, Hatef Darabi, Helga B. Salvesen, Heli Nevanlinna, Henrik Grönberg, Hermann Brenner, Hiltrud Brauch, Hoda Anton‐Culver, Honglin Song, Hui-Yi Lim, Iain A. McNeish, Ian Campbell, Ignace Vergote, Jacek Gronwald, Jan Lubiński, Janet L. Stanford, Javier Benı́tez, Jennifer A. Doherty, Jennifer B. Permuth, Jenny Chang‐Claude, Jenny Donovan, Joe Dennis, Joellen M. Schildkraut, Johanna Schleutker, John L. Hopper and 129 more - Cancer Discovery 2016 cited by 214
- The kinship2 R Package for Pedigree Data
Authors: Jason P. Sinnwell, Terry M. Therneau, Daniel J. Schaid - Human Heredity 2014 cited by 236
- Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study
Authors: Questa Karlsson, Mark N. Brook, Tokhir Dadaev, Sarah Wakerell, Edward J. Saunders, Kenneth Muir, David E. Neal, Graham G. Giles, Robert J. MacInnis, Stephen N. Thibodeau, Shannon K. McDonnell, Lisa Cannon‐Albright, Manuel R. Teixeira, Paula Paulo, Marta Cardoso, Chad D. Huff, Donghui Li, Yao Yu, Paul Scheet, Jennifer B. Permuth, Janet L. Stanford, James Y. Dai, Elaine A. Ostrander, Olivier Cussenot, Géraldine Cancel‐Tassin, Josef Hoegel, Kathleen Herkommer, Johanna Schleutker, Teuvo L.J. Tammela, Venkat Rathinakannan, Csilla Sipeky, Fredrik Wiklund, Henrik Grönberg, Markus Aly, William B. Isaacs, Joanne L. Dickinson, Liesel M. FitzGerald, Melvin L.K. Chua, Tú Nguyen‐Dumont, Daniel J. Schaid, Melissa C. Southey, Rosalind A. Eeles, Zsofia Kote‐Jarai - European Urology Oncology 2021 cited by 72
- Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study
Authors: Andrew M. Glazer, Giovanni Davogustto, Christian M. Shaffer, Carlos G. Vanoye, Reshma R. Desai, Eric Farber‐Eger, Ozan Dikilitas, Ning Shang, Jennifer A. Pacheco, Tao Yang, Ayesha Muhammad, Jonathan D. Mosley, Sara L. Van Driest, Quinn S. Wells, Lauren Lee Shaffer, Olivia R. Kalash, Yuko Wada, Harris T. Bland, Zachary T. Yoneda, Devyn Mitchell, Brett M. Kroncke, Iftikhar J. Kullo, Gail P. Jarvik, Allan Gordon, Eric B. Larson, Teri A. Manolio, Tooraj Mirshahi, Jonathan Z. Luo, Daniel J. Schaid, Bahram Namjou, Tarek Alsaied, Rajbir Singh, Ashutosh Singhal, Cong Liu, Chunhua Weng, George Hripcsak, James D. Ralston, Elizabeth M. McNally, Wendy K. Chung, David Carrell, Kathleen A. Leppig, Håkon Håkonarson, Patrick Sleiman, Sunghwan Sohn, Joseph Glessner, the eMERGE Network, Joshua C. Denny, Wei‐Qi Wei, Alfred L. George, M. Benjamin Shoemaker, Dan M. Roden - Circulation 2021 cited by 49
- Efficacy of Bilateral Prophylactic Mastectomy in Women with a Family History of Breast Cancer
Authors: Lynn C. Hartmann, Daniel J. Schaid, John E. Woods, T. P. Crotty, Jeffrey L. Myers, Phillip G. Arnold, Paul M. Petty, Thomas A. Sellers, Joanne L. Johnson, Shannon K. McDonnell, Marlene H. Frost, Clive S. Grant, Virginia V. Michels, Robert B. Jenkins - New England Journal of Medicine 1999 cited by 1,426
- Score Tests for Association between Traits and Haplotypes when Linkage Phase Is Ambiguous
Authors: Daniel J. Schaid, Charles M. Rowland, David E. Tines, Robert M. Jacobson, Gregory A. Poland - The American Journal of Human Genetics 2002 cited by 1,796
- Anxiety disorders and depressive disorders preceding Parkinson's disease: A case-control study
Authors: Mitsuru Shiba, James H. Bower, Demetrius M. Maraganore, Shannon K. McDonnell, Brett J. Peterson, J. Eric Ahlskog, Daniel J. Schaid, Walter A. Rocca - Movement Disorders 2000 cited by 465
- Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk
Authors: Daniel J. Schaid, Jason P. Sinnwell, Anthony Batzler, Shannon K. McDonnell - The American Journal of Human Genetics 2022 cited by 28
- Phase III evaluation of four doses of megestrol acetate as therapy for patients with cancer anorexia and/or cachexia.
Authors: Charles L. Loprinzi, J C Michalak, Daniel J. Schaid, J A Mailliard, Laureen M. Athmann, Richard M. Goldberg, Loren K. Tschetter, Alan K. Hatfield, Roscoe F. Morton - Journal of Clinical Oncology 1993 cited by 223
- HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)
Authors: Jianfeng Xu, Ethan M. Lange, Lingyi Lu, Siqun L. Zheng, Zhong Wang, Stephen N. Thibodeau, Lisa Cannon‐Albright, Craig C. Teerlink, Nicola J. Camp, Anna Johnson, Kimberly A. Zuhlke, Janet L. Stanford, Elaine A. Ostrander, Kathleen E. Wiley, Sarah D. Isaacs, Patrick C. Walsh, Christiane Maier, Manuel Luedeke, Walther Vogel, Johanna Schleutker, Tiina Wahlfors, Teuvo L.J. Tammela, Daniel J. Schaid, Shannon K. McDonnell, Melissa S. DeRycke, Géraldine Cancel‐Tassin, Olivier Cussenot, Fredrik Wiklund, Henrik Grönberg, Rosalind A. Eeles, Doug Easton, Zsofia Kote‐Jarai, Alice S. Whittemore, Chih-Lin Hsieh, Graham G. Giles, John L. Hopper, Gianluca Severi, William J. Catàlona, Diptasri Mandal, Elisa M. Ledet, William D. Foulkes, Nancy Hamel, Lovise Mahle, Pål Møller, Isaac J. Powell, Joan E. Bailey‐Wilson, John D. Carpten, Daniela Seminara, Kathleen A. Cooney, William B. Isaacs - Human Genetics 2012 cited by 198
- Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study
Authors: Yao Hu, Mariaelisa Graff, Jeffrey Haessler, Steven Buyske, Stephanie A. Bien, Ran Tao, Heather M. Highland, Katherine K. Nishimura, Niha Zubair, Yingchang Lu, Marie Verbanck, Austin T. Hilliard, Derek Klarin, Scott M. Damrauer, Yuk‐Lam Ho, the VA Million Veteran Program, Peter W.F. Wilson, Kyong‐Mi Chang, Philip S. Tsao, Kelly Cho, Christopher J. O’Donnell, Themistocles L. Assimes, Lauren E. Petty, Jennifer E. Below, Ozan Dikilitas, Daniel J. Schaid, Matthew Kosel, Iftikhar J. Kullo, Laura J. Rasmussen‐Torvik, Gail P. Jarvik, QiPing Feng, Wei‐Qi Wei, Eric B. Larson, Frank Mentch, Berta Almoguera, Patrick Sleiman, Laura M. Raffield, Adolfo Correa, Lisa W. Martin, Martha L. Daviglus, Tara C. Matise, José Luis Ambite, Christopher S. Carlson, Ron Do, Ruth J. F. Loos, Lynne R. Wilkens, Loı̈c Le Marchand, C.A. Haiman, Daniel O. Stram, Lucia A. Hindorff, Kari E. North, Charles Kooperberg, Iona Cheng, Ulrike Peters - PLoS Genetics 2020 cited by 33
- Development and Evaluation of a Comprehensive Prediction Model for Incident Coronary Heart Disease Using Genetic, Social, and Lifestyle–Psychological Factors: A Prospective Analysis of the UK Biobank
Authors: Mohammadreza Naderian, Kristján Norland, Daniel J. Schaid, Iftikhar Kullo - Annals of Internal Medicine 2024 cited by 26
