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Daniel J. Schaid

1987–2024 年に発表

155
論文数
33,853
被引用数
96
h 指数
153
i10 指数

被引用数

Daniel J. Schaid の年別被引用数1951 年: 被引用 1 件1972 年: 被引用 3 件1976 年: 被引用 1 件1980 年: 被引用 1 件1987 年: 被引用 2 件1989 年: 被引用 5 件1990 年: 被引用 6 件1991 年: 被引用 8 件1992 年: 被引用 6 件1993 年: 被引用 34 件1994 年: 被引用 89 件1995 年: 被引用 118 件1996 年: 被引用 109 件1997 年: 被引用 109 件1998 年: 被引用 144 件1999 年: 被引用 204 件2000 年: 被引用 239 件2001 年: 被引用 259 件2002 年: 被引用 259 件2003 年: 被引用 275 件2004 年: 被引用 319 件2005 年: 被引用 338 件2006 年: 被引用 346 件2007 年: 被引用 285 件2008 年: 被引用 354 件2009 年: 被引用 304 件2010 年: 被引用 286 件2011 年: 被引用 239 件2012 年: 被引用 194 件2013 年: 被引用 166 件2014 年: 被引用 155 件2015 年: 被引用 161 件2016 年: 被引用 162 件2017 年: 被引用 167 件2018 年: 被引用 199 件2019 年: 被引用 531 件2020 年: 被引用 545 件2021 年: 被引用 616 件2022 年: 被引用 518 件2023 年: 被引用 366 件2024 年: 被引用 716 件2025 年: 被引用 364 件2026 年: 被引用 26 件1952〜1971 年は被引用が無いため表示していません1973〜1975 年は被引用が無いため表示していません1977〜1979 年は被引用が無いため表示していません1981〜1986 年は被引用が無いため表示していません1988 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 4,375 件、この内訳の 29.8%イギリス: 引用元論文 1,275 件、この内訳の 8.7%ドイツ: 引用元論文 719 件、この内訳の 4.9%中国: 引用元論文 702 件、この内訳の 4.8%カナダ: 引用元論文 612 件、この内訳の 4.2%オーストラリア: 引用元論文 551 件、この内訳の 3.7%イタリア: 引用元論文 546 件、この内訳の 3.7%オランダ: 引用元論文 497 件、この内訳の 3.4%フランス: 引用元論文 492 件、この内訳の 3.3%スペイン: 引用元論文 373 件、この内訳の 2.5%スウェーデン: 引用元論文 355 件、この内訳の 2.4%日本: 引用元論文 334 件、この内訳の 2.3%
0%29.8%その他 26.3%

機関

分野

  • Medicine46.9%
  • Biochemistry, Genetics and Molecular Biology41.6%
  • Immunology and Microbiology3.2%
  • Neuroscience3.1%
  • Pharmacology, Toxicology and Pharmaceutics1%
  • Psychology0.8%
  • その他3.4%

トピック

  • 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%
  • その他77.7%

共著者

全論文

検索で開く
  1. REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

    著者: 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 被引用: 2,986

  2. From genome-wide associations to candidate causal variants by statistical fine-mapping

    著者: Daniel J. Schaid, Wenan Chen, Nicholas B. Larson - Nature Reviews Genetics 2018 被引用: 967

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

    著者: 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 被引用: 313

  4. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

    著者: 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 被引用: 189

  5. Genome-wide polygenic score to predict chronic kidney disease across ancestries

    著者: 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 被引用: 162

  6. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

    著者: 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 被引用: 173

  7. Microsatellite Instability in Cancer of the Proximal Colon

    著者: Stephen N. Thibodeau, Gary D. Bren, Daniel J. Schaid - Science 1993 被引用: 3,145

  8. Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates

    著者: 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 被引用: 270

  9. Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk

    著者: 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 被引用: 228

  10. Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics

    著者: Wenan Chen, Beth R. Larrabee, Inna G. Ovsyannikova, Richard B. Kennedy, Iana H. Haralambieva, Gregory A. Poland, Daniel J. Schaid - Genetics 2015 被引用: 261

  11. Risk tables for parkinsonism and Parkinson's disease

    著者: 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 被引用: 376

  12. Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups

    著者: 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 被引用: 173

  13. Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

    著者: 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 ほか 129 名 - Cancer Discovery 2016 被引用: 214

  14. The kinship2 R Package for Pedigree Data

    著者: Jason P. Sinnwell, Terry M. Therneau, Daniel J. Schaid - Human Heredity 2014 被引用: 236

  15. Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study

    著者: 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 被引用: 72

  16. Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study

    著者: 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 被引用: 49

  17. Efficacy of Bilateral Prophylactic Mastectomy in Women with a Family History of Breast Cancer

    著者: 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 被引用: 1,426

  18. Score Tests for Association between Traits and Haplotypes when Linkage Phase Is Ambiguous

    著者: Daniel J. Schaid, Charles M. Rowland, David E. Tines, Robert M. Jacobson, Gregory A. Poland - The American Journal of Human Genetics 2002 被引用: 1,796

  19. Anxiety disorders and depressive disorders preceding Parkinson's disease: A case-control study

    著者: 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 被引用: 465

  20. Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk

    著者: Daniel J. Schaid, Jason P. Sinnwell, Anthony Batzler, Shannon K. McDonnell - The American Journal of Human Genetics 2022 被引用: 28

  21. Phase III evaluation of four doses of megestrol acetate as therapy for patients with cancer anorexia and/or cachexia.

    著者: 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 被引用: 223

  22. HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)

    著者: 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 被引用: 198

  23. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

    著者: 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 被引用: 33

  24. 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

    著者: Mohammadreza Naderian, Kristján Norland, Daniel J. Schaid, Iftikhar Kullo - Annals of Internal Medicine 2024 被引用: 26