Howard J. Jacob

Active 1991–2025

120
Papers
24,945
Citations
82
h-index
116
i10-index

Citations

Citations per year for Howard J. Jacob1992: 13 citations1993: 17 citations1994: 31 citations1995: 38 citations1996: 50 citations1997: 60 citations1998: 79 citations1999: 70 citations2000: 106 citations2001: 86 citations2002: 167 citations2003: 163 citations2004: 175 citations2005: 165 citations2006: 156 citations2007: 106 citations2008: 124 citations2009: 130 citations2010: 138 citations2011: 146 citations2012: 162 citations2013: 223 citations2014: 215 citations2015: 186 citations2016: 157 citations2017: 178 citations2018: 174 citations2019: 467 citations2020: 488 citations2021: 461 citations2022: 456 citations2023: 506 citations2024: 1,129 citations2025: 451 citations2026: 16 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,345 citing papers, 29.2% of this breakdownChina: 1,306 citing papers, 11.4% of this breakdownUnited Kingdom: 960 citing papers, 8.4% of this breakdownGermany: 628 citing papers, 5.5% of this breakdownCanada: 432 citing papers, 3.8% of this breakdownFrance: 397 citing papers, 3.4% of this breakdownAustralia: 327 citing papers, 2.8% of this breakdownItaly: 318 citing papers, 2.8% of this breakdownNetherlands: 299 citing papers, 2.6% of this breakdownJapan: 297 citing papers, 2.6% of this breakdownSweden: 261 citing papers, 2.3% of this breakdownFinland: 228 citing papers, 2% of this breakdown
0%29.2%Other 23.2%

Fields

  • Biochemistry, Genetics and Molecular Biology58.5%
  • Medicine27.4%
  • Neuroscience3.7%
  • Immunology and Microbiology2.7%
  • Agricultural and Biological Sciences1.9%
  • Nursing1.7%
  • Other4.1%

Topics

  • Genetic Associations and Epidemiology5.3%
  • Genomics and Rare Diseases3.2%
  • Genetic Mapping and Diversity in Plants and Animals2.4%
  • Extracellular vesicles in disease2.3%
  • Bioinformatics and Genomic Networks2%
  • MicroRNA in disease regulation1.9%
  • Other82.9%

Coauthors

All papers

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  1. FinnGen provides genetic insights from a well-phenotyped isolated population

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin B. Sun, Christopher N. Foley, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, FinnGen, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja and 69 more - Nature 2023 cited by 4,257

  2. Characterization of human plasma-derived exosomal RNAs by deep sequencing

    Authors: , , , , , , , , , , , , , - BMC Genomics 2013 cited by 1,067

  3. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Huy Nguyen, Cara Mason, Christopher Farnham, Charlotte Tolonen, Laura D. Gauthier, Namrata Gupta, Daniel G. MacArthur, Heidi L. Rehm, Cotton Seed, Anthony Philippakis, Mark J. Daly, J. Wade Davis, Heiko Runz, Melissa Miller, Benjamin M. Neale - Cell Genomics 2022 cited by 295

  4. Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt and 11 more - Nature Genetics 2021 cited by 427

  5. FinnGen: Unique genetic insights from combining isolated population and national health register data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja, Sahar V. Mozaffari, Mari Niemi, Marianna Niemi and 66 more - medRxiv 2022 cited by 412

  6. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael F. Wangler, Monte Westerfield, Matthew T. Wheeler, Anastasia L. Wise, Elizabeth A. Worthey, Shinya Yamamoto, Euan A. Ashley - New England Journal of Medicine 2018 cited by 374

  7. Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ene Reimann, Bindu Swapna Madala, Tim R. Mercer, Chris Miller, Howard J. Jacob, Tiffany Truong, Ali Moshrefi, Aparna Natarajan, Ana Granat, Gary P. Schroth, Rasika Kalamegham, Eric Peters, Virginie Petitjean, Ashley Walton, Tsai-Wei Shen, Keyur Talsania, Cristobal Juan Vera, Kurt J. Langenbach, Maryellen de Mars, Jennifer Hipp, James C. Willey, Jing Wang, Jyoti Shetty, Yuliya Kriga, Arati Raziuddin, Bao Tran, Yuanting Zheng, Ying Yu, Margaret C. Cam, Parthav Jailwala, Cu Nguyen, Daoud Meerzaman, Qingrong Chen, Chunhua Yan, Ben Ernest, Urvashi Mehra, Roderick V. Jensen, Wendell Jones, Jian‐Liang Li, Brian N. Papas, Mehdi Pirooznia, Yunching Chen, Fayaz Seifuddin, Zhipan Li, Xue‐Lu Liu, Wolfgang Resch, Jingya Wang, Leihong Wu, Gökhan Yavaş, Corey J. Miles, Baitang Ning, Weida Tong, Christopher E. Mason, Eric Donaldson, Samir Lababidi, Louis M. Staudt, Živana Težak, Huixiao Hong, Charles Wang, Leming Shi - Nature Biotechnology 2021 cited by 213

  8. Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Satu Wedenoja, Satu Leminen, Aija Lähdesmäki, Susanna Mehtälä, Christina Salmén, Aarno Palotie, Mark J. Daly, Bridget Riley-Gills, Howard J. Jacob, Dirk S. Paul, Athena Matakidou, Adam Platt, Heiko Runz, Sally John, George Okafo, Nathan Lawless, Robert M. Plenge, Joseph Maranville, Mark I. McCarthy, Julie Hunkapiller, Margaret G. Ehm, Kirsi Auro, Simonne Longerich, Caroline S. Fox, Anders Mälarstig, K. Klinger, Deepak Raipal, Eric Green, Robert Graham, Robert Yang, Chris O ́Donnell, Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Antti Hakanen, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Juhani Junttila, Raisa Serpi, Tarja Laitinen, Veli‐Matti Kosma, Jari A. Laukkanen, Marco Hautalahti, Outi Tuovila, Raimo Pakkanen, Jeffrey F. Waring, Bridget Riley‐Gillis, Fedik Rahimov, Ioanna Tachmazidou, Chia‐Yen Chen, Zhihao Ding, Marc Jung, Shameek Biswas, Rion Pendergrass, David Pulford, Neha Raghavan, Adriana Huertas‐Vázquez, Jae-Hoon Sul, Xinli Hu, Sahar V. Mozaffari, Dawn Waterworth, Nicole Renaud, Ma ́en Obeidat, Johanna Schleutker, Mikko Arvas, Olli Carpén, Reetta Hinttala, Arto Mannermaa and 259 more - JAMA Cardiology 2023 cited by 131

  9. The role of polygenic risk and susceptibility genes in breast cancer over the course of life

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mervi Aavikko, Mitja Kurki, Oluwaseun Alexander Dada, Pietro Della Briotta Parolo, Risto Kajanne, Sina Rüeger, Susanna Lemmelä, Taru Tukiainen, Tiinamaija Tuomi, Timo P. Sipilä, Tuomo Kiiskinen, Vincent Llorens, Adam Ziemann, Anne Lehtonen, Apinya Lertratanakul, Bob Georgantas, Bridget Riley‐Gillis, Danjuma Quarless, Fedik Rahimov, Howard J. Jacob, Jeffrey F. Waring, J. Wade Davis, Nizar Smaoui, Relja Popovic, Sahar Esmaeeli, Athena Matakidou, Ben Challis, David A. Close, Eleonor Wigmore, Slavé Petrovski, Chia‐Yen Chen, Ellen Tsai, Heiko Runz, Jimmy Z. Liu, Paola G. Bronson, Sally John, Sanni Lahdenperä, Stephanie Loomis, Susan Eaton, Yunfeng Huang, Erika Kvikstad, Minal Çalışkan, Samir Wadhawan, Elmutaz Shaikho Elhaj Mohammed, Janet van Adelsberg, Joseph Maranville, Marla Hochfeld, Robert M. Plenge, Shameek Biswas, Steven M. Greenberg, Andrew S. Peterson, David F. Choy, Diana Chang, Edmond Teng, Erich C. Strauss, Geoff Kerchner, Hao Chen, Hubert Chen, Jennifer L. Schutzman, John A. Michon, Julie Hunkapiller, Mark I. McCarthy, Natalie Bowers, Sarah A. Pendergrass, Tushar Bhangale, David Pulford, Dawn Waterworth, Diptee Kulkarni, Fanli Xu, Jo Betts and 180 more - Nature Communications 2020 cited by 173

  10. Systematic single-variant and gene-based association testing of thousands of phenotypes in 426,370 UK Biobank exomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Huy Nguyen, Cara Mason, Christopher Farnham, Charlotte Tolonen, Laura D. Gauthier, Namrata Gupta, Daniel G. MacArthur, Heidi L. Rehm, Cotton Seed, Anthony Philippakis, Mark J. Daly, J. Wade Davis, Heiko Runz, Melissa Miller, Benjamin M. Neale - medRxiv 2021 cited by 62

  11. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Arto Lehistö, Elina Kilpeläinen, Georg Brein, Awaisa Ghazal, Jarmo Harju, Kalle Pärn, Pietro Della Briotta Parolo, Risto Kajanne, Susanna Lemmelä, Timo P. Sipilä, Tuomas Sipilä, Ulrike Lyhs, Vincent Llorens, Teemu Niiranen, Kati Kristiansson, Lotta Männikkö, Manuel González Jiménez, Markus Perola, Regis Wong, Terhi Kilpi, Tero Hiekkalinna, Elina Järvensivu, Essi Kaiharju, Hannele Mattsson, Markku Laukkanen, Päivi Laiho, Sini Lähteenmäki, Tuuli Sistonen, Sirpa Soini, Adam Ziemann, Anne Lehtonen, Apinya Lertratanakul, Bob Georgantas, Bridget Riley‐Gillis, Danjuma Quarless, Fedik Rahimov, Graham Heap, Howard J. Jacob, Jeffrey F. Waring, J. Wade Davis, Nizar Smaoui, Relja Popovic, Sahar Esmaeeli, Jeff Waring, Athena Matakidou, Ben Challis, David A. Close, Slavé Petrovski, Antti Karlsson, Johanna Schleutker, Kari Pulkki, Petri Virolainen, Lila Kallio, Arto Mannermaa, Sami Heikkinen, Veli‐Matti Kosma, Chia‐Yen Chen, Heiko Runz, Jimmy Liu, Paola G. Bronson, Sally John, Sanni Lahdenperä, Susan Eaton, Wei Zhou, Minna Hendolin, Outi Tuovila, Raimo Pakkanen, Joseph Maranville, Keith Usiskin, Marla Hochfeld and 161 more - Nature Communications 2019 cited by 195

  12. The Collaborative Cross, a community resource for the genetic analysis of complex traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Doug Matthews, Melloni N. Cook, Roger Cox, John C. Crabbe, Wim E. Crusio, Ariel Darvasi, Christian F. Deschepper, Bastien Llamas, R. W. Doerge, Charles R. Farber, Juan F. Medrano, Jiřı́ Forejt, Daniel P. Gaile, Steven J. Garlow, Hartmut Geiger, Howard K. Gershenfeld, Terry Gordon, Weikuan Gu, Gerald de Haan, Richard S. Nowakowski, Nancy L. Hayes, Craig Heller, Heinz Himmelbauer, Kent W. Hunter, Hui-Chen Hsu, Fuad A. Iraqi, Boris Ivandic, Howard J. Jacob, Ritsert C. Jansen, Karl J. Jepsen, Dabney K. Johnson, Gerd Kempermann, Christina Kendziorski, Malak Kotb, R. Frank Kooy, Frank Lammert, Jean‐Michel Lassalle, Pedro R. Löwenstein, Aldons J. Lusis, Kenneth F. Manly, Ralph Marcucio, Darla R. Miller, Beverly A. Mock, Jeffrey S. Mogil, Xavier Montagutelli, Grant Morahan, D.G. Morris, Richard Mott, William Valdar, Joseph H. Nadeau, Hiroki Nagase, Bruce F. O’Hara, А. В. Осадчук, Nengjun Yi, Grier P. Page, Abraham A. Palmer, Leena Peltonen-Palotie, Daniel Pomp, Daniel Pomp, Michal Pravenec, Daniel R. Prows, Zhonghua Qi, Roger H. Reeves, John Roder, Glenn D. Rosen, Eric E. Schadt, Leonard C. Schalkwyk, Ze’ev Seltzer, Kazuhiro Shimomura, Siming Shou and 13 more - Nature Genetics 2004 cited by 1,193

  13. Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Athena Matakidou, Heiko Runz, Sally John, Robert M. Plenge, Mark I. McCarthy, Julie Hunkapiller, Meg Ehm, Dawn Waterworth, Caroline S. Fox, Anders Mälarstig, Kathy Klinger, Kathy Call, Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Kari Pulkki, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Riitta Kaarteenaho, Seppo Vainio, Kimmo Savinainen, Veli‐Matti Kosma, Urho M. Kujala, Other experts and non-voting members, Outi Tuovila, Minna Hendolin, Raimo Pakkanen, Pharmaceutical companies, Jeff Waring, Bridget Riley‐Gillis, Athena Matakidou, Heiko Runz, Jimmy Z. Liu, Shameek Biswas, Julie Hunkapiller, Dawn Waterworth, Meg Ehm, Dorothée Diogo, Caroline S. Fox, Anders Mälarstig, Catherine Marshall, Xinli Hu, Kathy Call, Kathy Klinger, Matthias Gossel, Samuli Ripatti, Johanna Schleutker, Markus Perola, Mikko Arvas, Olli Carpén, Reetta Hinttala, Johannes Kettunen, Reijo Laaksonen, Arto Mannermaa, Urho M. Kujala, Other experts and non-voting members, Outi Tuovila, Minna Hendolin, Raimo Pakkanen, Neurology group, Hilkka Soininen, Valtteri Julkunen, Anne M. Remes, Reetta Kälviäinen, Mikko Hiltunen, Jukka Peltola, Pentti J. Tienari, Juha O. Rinne and 332 more - Nature 2020 cited by 148

  14. Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin B. Sun, Christopher N. Foley, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, FinnGen, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja and 69 more - Nature 2023 cited by 121

  15. Advancing Human Genetics Research and Drug Discovery through Exome Sequencing of the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid - medRxiv 2020 cited by 96

  16. The landscape of GWAS validation; systematic review identifying 309 validated non-coding variants across 130 human diseases

    Authors: , , , , , , , , , - BMC Medical Genomics 2022 cited by 83

  17. Knockout Rats via Embryo Microinjection of Zinc-Finger Nucleases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2009 cited by 927

  18. Rats!

    Authors: , - Disease Models & Mechanisms 2009 cited by 242

  19. Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Fabio Pizza, Monica Moresco, Catherine Crowe, Stephen K. Van Den Eeden, Michel Lecendreux, Patrice Bourgin, Takashi Kanbayashi, F Martínez-Orozco, Rosa Peraita‐Adrados, Antonio Benetó, Jacques Montplaisir, Alex Désautels, Yu‐Shu Huang, FinnGen, Thomas D. Als, Adam Ziemann, Ali Abbasi, Anne Lehtonen, Apinya Lertratanakul, Bridget Riley‐Gillis, Fedik Rahimov, Howard J. Jacob, Jeffrey F. Waring, Mengzhen Liu, Nizar Smaoui, Relja Popovic, Adam Platt, Athena Matakidou, Benjamin Challis, Dirk S. Paul, Glenda Lassi, Ioanna Tachmazidou, Antti Hakanen, Johanna Schleutker, Nina Pitkänen, Perttu Terho, Petri Virolainen, Arto Mannermaa, Veli‐Matti Kosma, Chia‐Yen Chen, Heiko Runz, Sally John, Sanni Lahdenperä, Stephanie Loomis, Susan Eaton, George Okafo, Heli Salminen‐Mankonen, Marc Jung, Nathan Lawless, Zhihao Ding, Joseph Maranville, Marla Hochfeld, Robert M. Plenge, Shameek Biswas, Masahiro Kanai, Mutaamba Maasha, Wei Zhou, Outi Tuovila, Raimo Pakkanen, Jari A. Laukkanen, Teijo Kuopio, Kristiina Aittomäki, Antti Mäkitie, Natalia Pujol, Triin Laisk, Katriina Aalto‐Setälä, Johanna Mäkelä, Marco Hautalahti, Sarah Smith, Tom Southerington and 312 more - Nature Communications 2023 cited by 61

  20. Comparative Recombination Rates in the Rat, Mouse, and Human Genomes

    Authors: , , , , , , , , - Genome Research 2004 cited by 567

  21. MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Donna M. Brown, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Katherine R. Chao, Gary Clark, Joy D. Cogan, Cynthia M. Cooper, William J. Craigen, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Katrina M. Dipple, Laurel A. Donnell‐Fink, Naghmeh Dorrani, Daniel C. Dorset, David D. Draper, Annika M. Dries, David J. Eckstein, Lisa Emrick, Christine M. Eng, Cecilia Esteves, Tyra Estwick, Paul G. Fisher, Trevor S. Frisby, Kate Frost, William A. Gahl, Valerie Gartner, Rena A. Godfrey, Mitchell Goheen, Gretchen Golas, David Goldstein, Mary “Gracie” G. Gordon, Sarah E. Gould, Jean-Philippe F. Gourdine, Brett H. Graham, Catherine Groden, Andrea Gropman, Mary E. Hackbarth, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Lori H. Handley, Isabel Hardee, Matthew Herzog, Ingrid A. Holm, Ellen M. Howerton, Howard J. Jacob, Mahim Jain, Yong‐hui Jiang, Jean M. Johnston, Angela Jones, Alanna E. Koehler, David M. Koeller, Isaac S. Kohane, Jennefer N. Kohler, Donna M. Krasnewich, Elizabeth L. Krieg, Joel B. Krier, Jennifer Kyle, Seema R. Lalani, Lea Latham, Yvonne L. Latour, C. Christopher Lau, Jozef Lazar, Brendan Lee, Hane Lee, Paul R. Lee, Shawn Levy and 87 more - The American Journal of Human Genetics 2017 cited by 223

  22. The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lauren C. Briere, Donna M. Brown, Catherine A. Brownstein, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Katherine R. Chao, Gary Clark, Joy D. Cogan, Cynthia M. Cooper, William J. Craigen, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Katrina M. Dipple, Laurel A. Donnell‐Fink, Naghmeh Dorrani, Daniel C. Dorset, David D. Draper, Annika M. Dries, Rachel L. Eastwood, David J. Eckstein, Lisa Emrick, Christine M. Eng, Cecilia Esteves, Tyra Estwick, Paul G. Fisher, Trevor S. Frisby, Kate Frost, William A. Gahl, Valerie Gartner, Rena A. Godfrey, Mitchell Goheen, Gretchen Golas, David B. Goldstein, Mary “Gracie” G. Gordon, Sarah E. Gould, Jean-Philippe F. Gourdine, Brett H. Graham, Catherine Groden, Andrea Gropman, Mary E. Hackbarth, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Lori H. Handley, Isabel Hardee, Matthew Herzog, Ingrid A. Holm, Ellen M. Howerton, Brenda Iglesias, Howard J. Jacob, Mahim Jain, Yong‐hui Jiang, Jean M. Johnston, Angela Jones, Alanna E. Koehler, David M. Koeller, Isaac S. Kohane, Jennefer N. Kohler, Donna M. Krasnewich, Elizabeth L. Krieg, Joel B. Krier, Jennifer Kyle, Seema R. Lalani, Lea Latham, Yvonne L. Latour, C. Christopher Lau, Jozef Lazar and 92 more - The American Journal of Human Genetics 2017 cited by 188

  23. Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Antti Hakanen, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Juhani Junttila, Raisa Serpi, Tarja Laitinen, Veli‐Matti Kosma, Arto Mannermaa, Jari Laukkanen, Marco Hautalahti, Other Experts/Non-Voting Members, Outi Tuovila, Raimo Pakkanen, Pharmaceutical companies, Jeffrey Waring, Ioanna Tachmazidou, Chia-Yen Chen, Shameek Biswas, Zhihao Ding, Marc Jung, Rion Pendergrass, David Pulford, Neha Raghavan, Adriana Huertas‐Vázquez, Jae-Hoon Sul, Xinli Hu, Sahar V. Mozaffari, Dawn Waterworth, Nicole Renaud, Ma ́en Obeidat, Samuli Ripatti, Johanna Schleutker, Mikko Arvas, Olli Carpén, Reetta Hinttala, Johannes Kettunen, Katriina Aalto‐Setälä, Mika Kähönen, Johanna Mäkelä, Neurology Group, Reetta Kälviäinen, Valtteri Julkunen, Hilkka Soininen, Anne M. Remes, Mikko Hiltunen, Jukka Peltola, Pentti J. Tienari, Juha O. Rinne, Roosa Kallionpää, Ali Abbasi, Adam Ziemann, Sahar Esmaeeli, Nizar Smaoui, Anne Lehtonen, Susan Eaton, Sanni Lahdenperä, Janet van Adelsberg, Natalie Bowers, Edmond Teng, Sarah A. Pendergrass, Onuralp Söylemez, Kari Linden, Fanli Xu, Laura Addis, John D. Eicher and 290 more - Communications Biology 2022 cited by 51

  24. Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gabriel F. Batzli, Alan H. Beggs, Babak Behnam, Anna Bican, David Bick, Camille L. Birch, Devon Bonner, Braden Boone, Bret L. Bostwick, Lauren C. Briere, Donna M. Brown, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Shan Chen, Gary Clark, Terra R. Coakley, Joy D. Cogan, Cynthia M. Cooper, Heidi Cope, William J. Craigen, Precilla D’Souza, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Ani Dillon, Katrina M. Dipple, Laurel A. Donnell‐Fink, Naghmeh Dorrani, Daniel C. Dorset, Emilie D. Douine, David D. Draper, David J. Eckstein, Lisa Emrick, Christine M. Eng, Ascia Eskin, Cecilia Esteves, Tyra Estwick, Carlos R. Ferreira, Brent L. Fogel, Noah D. Friedman, William A. Gahl, Emily Glanton, Rena A. Godfrey, David B. Goldstein, Sarah E. Gould, Jean-Philippe F. Gourdine, Catherine Groden, Andrea Gropman, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Lori H. Handley, Matthew Herzog, Ingrid A. Holm, Jason Hom, Ellen M. Howerton, Yong Huang, Howard J. Jacob, Mahim Jain, Yong‐hui Jiang, Jean M. Johnston, Angela Jones, Isaac S. Kohane, Donna M. Krasnewich, Elizabeth L. Krieg, Joel B. Krier, Seema R. Lalani, C. Christopher Lau and 116 more - The American Journal of Human Genetics 2018 cited by 107