ScholarIQanswers from OpenAlex & ORCID
Kenneth Rice
ResearcherPublications, citations & collaboration network
Kenneth Rice is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Kenneth Rice have?
ScholarIQindexed works
Kenneth Rice has 421 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Kenneth Rice have?
ScholarIQcitation count
Kenneth Rice has 48,347 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Kenneth Rice?
ScholarIQh-index
Kenneth Rice has an h-index of 106 in OpenAlex.
What is the i10-index of Kenneth Rice?
ScholarIQi10-index
Kenneth Rice has an i10-index of 283 in OpenAlex.
What is the ORCID of Kenneth Rice?
ScholarIQorcid
The ORCID for Kenneth Rice is on the source record.
What is the OpenAlex record for Kenneth Rice?
ScholarIQopenalex
The OpenAlex for Kenneth Rice is on the source record.
What are the most-cited papers on Kenneth Rice?
ScholarIQmost cited works
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg Ehret, Vasyl Pihur, Khanh-Dung Hoang Nguyen, Dan E. Arking, Gina Hilton, A Chakravarti, Murielle Bochud, P Munroe, Sue Shaw‐Hawkins, Mark J. Caulfield, Toby Johnson, Kenneth Rice, Andrew D. Johnson, Shih-Jen Hwang, Thomas J. Wang, R VASAN, M G Larson, Daniel Levy, Daniel I. Chasman, P M Ridker, Christopher J. O’Donnell, Albert V. Smith, Thor Aspelund, Vilmundur Guðnason, Martin D. Tobin, Paul R. Burton, María Soler Artigas, Nick Shrine, Louise V. Wain, Germaine C. Verwoert, Najaf Amin, Yurii S. Aulchenko, Abbas Dehghan, M. Arfan Ikram, A Hofman, Francesco Mattace‐Raso, Ayşe Demirkan, Aaron Isaacs, Fernando Rivadeneira, Eric J.G. Sijbrands, André G. Uitterlinden, Jacqueline C.M. Witteman, Cornelia M. van Duijn, Péter Vollenweider, Paul F. O’Reilly, John C. Chambers, Weihua Zhang, Peter Würtz, Marjo-Riitta Järvelin, Paul Elliott, Jennifer L. Bragg‐Gresham, Abecasis Gb, Alexander Teumer, Uwe Völker, Nicole L. Glazer, Joshua C. Bis, B M Psaty, Lenore Launer, Melissa N. Garcia, T H S Harris, Jing Zhao, Jian’an Luan, Ruth J. F. Loos, Nicholas J. Wareham, Simon Heath, Mark Lathrop, Diana Zélénika, Siim Sõber, Elin Org, Gudrun Veldre, Maris Laan, Afshin Parsa, Weihua Zhang, Jeffrey R. O’Connell, Nanette Steinle, Alan R. Shuldiner, Pankaj Arora, Sekar Kathiresan, Christopher Newton‐Cheh, Feng Zhang, Massimo Mangino, Tim D. Spector, Guangju Zhai, N Soranzo, Gavin Lucas, Roberto Elosua, Andrew A. Hicks, Cristian Pattaro, P Pramstaller, Anne Jackson, Laura J. Scott, Heather M. Stringham, Michael Boehnke, John F. Peden, Halit Ongen, Anuj Goel, Hugh Watkins, Martin Farrall, Toshiko Tanaka, Yuri Milaneschi
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Thomas J. Wang, Feng Zhang, J. Brent Richards, Bryan Kestenbaum, Joyce B. J. van Meurs, Diane J. Berry, Douglas P. Kiel, Elizabeth A. Streeten, Claes Ohlsson, Daniel L. Koller, Leena Peltonen, Jason D. Cooper, Paul F. O’Reilly, Denise K. Houston, Nicole L. Glazer, Liesbeth Vandenput, Munro Peacock, Julia Shi, Fernando Rivadeneira, Mark I. McCarthy, Anneli Pouta, Ian H. de Boer, Massimo Mangino, Bernet Kato, Deborah J. Smyth, Sarah L. Booth, Paul F. Jacques, Greg Burke, Mark O. Goodarzi, Ching‐Lung Cheung, Myles Wolf, Kenneth Rice, David Goltzman, Nick Hidiroglou, Martin Ladouceur, Nicholas J. Wareham, Lynne J. Hocking, Deborah Hart, Nigel Arden, Cyrus Cooper, Suneil Malik, William D. Fraser, Anna-Liisa Hartikainen, Guangju Zhai, Helen M. Macdonald, Nita G. Forouhi, Ruth J. F. Loos, David M. Reid, Alan J. Hakim, Elaine Dennison, Ching‐Ti Liu, Chris Power, Helen E. Stevens, Laitinen Jaana, Ramachandran S. Vasan, Nicole Soranzo, Jörg Bojunga, Bruce M. Psaty, Mattias Lorentzon, Tatiana Foroud, Tamara B. Harris, Albert Hofman, John-Olov Jansson, Jane A. Cauley, André G. Uitterlinden, Quince Gibson, Marjo‐Riitta Järvelin, David Karasik, David S. Siscovick, Michael J. Econs, Stephen B. Kritchevsky, José C. Florez, John A. Todd, Josée Dupuis, Elina Hyppönen, Timothy D. Spector
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
Richa Saxena, the MAGIC investigators, Marie‐France Hivert, Claudia Langenberg, Toshiko Tanaka, James S. Pankow, Péter Vollenweider, Valeriya Lyssenko, Nabila Bouatia‐Naji, Josée Dupuis, Anne Jackson, W.H. Linda Kao, Man Li, Nicole L. Glazer, Alisa K Manning, Jian’an Luan, Heather M. Stringham, Inga Prokopenko, Toby Johnson, Niels Grarup, Trine Welløv Boesgaard, Cécile Lecoeur, Peter Shrader, Jeffrey R. O’Connell, Erik Ingelsson, David Couper, Kenneth Rice, Kijoung Song, Camilla Andreasen, Christian Dina, Anna Köttgen, Olivier Le Bacquer, François Pattou, Jalal Taneera, Valgerður Steinthórsdóttir, Denis Rybin, Kristin Ardlie, Michael Sampson, Lu Qi, Mandy van Hoek, Michael N. Weedon, Yurii S. Aulchenko, Benjamin F. Voight, Harald Grallert, Beverley Balkau, Richard N. Bergman, Suzette J. Bielinski, Amélie Bonnefond, Lori L. Bonnycastle, Knut Borch‐Johnsen, Yvonne Böttcher, Eric J. Brunner, Thomas A. Buchanan, Suzannah J. Bumpstead, Christine Cavalcanti-Proença, G. Charpentier, Yii-Der Ida Chen, Peter S. Chines, Francis S. Collins, Marilyn C. Cornelis, Gabriel Crawford, Jérôme Delplanque, Alex S. F. Doney, Josephine M. Egan, Michael R. Erdos, Mathieu Firmann, Nita G. Forouhi, Caroline S. Fox, Mark O. Goodarzi, Jürgen Graessler, Aroon D. Hingorani, Bo Isomaa, Torben Jørgensen, Mika Kivimäki, Péter Kovács, Knut Krohn, Meena Kumari, Torsten Lauritzen, Claire Lévy‐Marchal, Vladimir Mayor, Jarred B. McAteer, Stephen Eyre, Braxton D. Mitchell, Karen L. Mohlke, Mario A. Morken, Narisu Narisu, Colin N A Palmer, Ruth Pakyz, Laura Pascoe, Felicity Payne, Daniel S. Pearson, Wolfgang Rathmann, Annelli Sandbæk, Avan Aihie Sayer, Laura J. Scott, Stephen J. Sharp, Eric J.G. Sijbrands, Andrew B. Singleton, David S. Siscovick, Nicholas L. Smith
Genetic Loci Associated with Plasma Phospholipid n-3 Fatty Acids: A Meta-Analysis of Genome-Wide Association Studies from the CHARGE Consortium
Rozenn N. Lemaître, Toshiko Tanaka, Weihong Tang, Ani Manichaikul, Millennia Foy, Edmond K. Kabagambe, Jennifer A. Nettleton, Irena B. King, Lu-Chen Weng, Sayanti Bhattacharya, Stefania Bandinelli, Joshua C. Bis, Stephen S. Rich, David R. Jacobs, Antonio Cherubini, Barbara McKnight, Shuang Liang, Xiangjun Gu, Kenneth Rice, Cathy C. Laurie, Thomas Lumley, Brian L. Browning, Bruce M. Psaty, Yii-Der I. Chen, Yechiel Friedlander, Luc Djoussé, Jason Wu, David S. Siscovick, André G. Uitterlinden, Donna K. Arnett, Luigi Ferrucci, Myriam Fornage, Michael Y. Tsai, Dariush Mozaffarian, Lyn M. Steffen
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Emelia J. Benjamin, Kenneth Rice, Dan E. Arking, Arne Pfeufer, Charlotte van Noord, Albert V. Smith, Renate B. Schnabel, Joshua C Bis, Eric Boerwinkle, Moritz F. Sinner, Abbas Dehghan, Steven A. Lubitz, Ralph B. D’Agostino, Thomas Lumley, Georg Ehret, Jan Heeringa, Thor Aspelund, Christopher Newton‐Cheh, Martin G. Larson, Kristin D. Marciante, Elsayed Z. Soliman, Fernando Rivadeneira, Thomas J. Wang, Guðný Eiríksdóttir, Daniel Levy, Bruce M. Psaty, Man Li, Alanna M. Chamberlain, Albert Hofman, Ramachandran S. Vasan, Tamara B. Harris, Jerome I. Rotter, W.H. Linda Kao, Sunil Agarwal, Bruno H. Stricker, Ke Wang, Lenore J. Launer, Nicholas L. Smith, Aravinda Chakravarti, André G. Uitterlinden, Philip A. Wolf, Nona Sotoodehnia, Anna Köttgen, Cornelia M. van Duijn, Thomas Meitinger, Martina Mueller, Siegfried Perz, Gerhard Steinbeck, H‐Erich Wichmann, Kathryn L. Lunetta, Susan R. Heckbert, Vilmundur Guðnason, Álvaro Alonso, Stefan Kääb, Patrick T. Ellinor, Jacqueline C.M. Witteman