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Sara L. Pulit

ResearcherPublications, citations & collaboration network

Sara L. Pulit is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Sara L. Pulit have?

ScholarIQindexed works

Sara L. Pulit has 181 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Sara L. Pulit have?

ScholarIQcitation count

Sara L. Pulit has 19,116 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Sara L. Pulit?

ScholarIQh-index

Sara L. Pulit has an h-index of 50 in OpenAlex.

What is the i10-index of Sara L. Pulit?

ScholarIQi10-index

Sara L. Pulit has an i10-index of 89 in OpenAlex.

What is the ORCID of Sara L. Pulit?

ScholarIQorcid

The ORCID for Sara L. Pulit is on the source record.

What is the OpenAlex record for Sara L. Pulit?

ScholarIQopenalex

The OpenAlex for Sara L. Pulit is on the source record.

What are the most-cited papers on Sara L. Pulit?

ScholarIQmost cited works
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Rainer Malik, Ganesh Chauhan, Matthew Traylor, Muralidharan Sargurupremraj, Yukinori Okada, Aniket Mishra, Loes C.A. Rutten‐Jacobs, Anne-Katrin Giese, Sander W. van der Laan, Sólveig Grétarsdóttir, Christopher D. Anderson, Michael Chong, Hieab H.H. Adams, Tetsuro Ago, Peter Almgren, Philippe Amouyel, Hakan Ay, Traci M. Bartz, Oscar R. Benavente, Steve Bevan, Giorgio B. Boncoraglio, Robert D. Brown, Adam S. Butterworth, Caty Carrera, Cara L. Carty, Daniel I. Chasman, Wei‐Min Chen, John W. Cole, Adolfo Correa, Ioana Cotlarciuc, Carlos Cruchaga, John Danesh, Paul I. W. de Bakker, Anita L. DeStefano, Marcel den Hoed, Qing Duan, Stefan T. Engelter, Guido J. Falcone, Rebecca F. Gottesman, Raji P. Grewal, Vilmundur Guðnason, Stefan Gustafsson, Jeffrey Haessler, Tamara B. Harris, Ahamad Hassan, Aki S. Havulinna, Susan R. Heckbert, Elizabeth G. Holliday, George Howard, Fang‐Chi Hsu, Hyacinth I. Hyacinth, M. Arfan Ikram, Erik Ingelsson, Marguerite R. Irvin, Xueqiu Jian, Jordi Jiménez‐Conde, Julie A. Johnson, J. Wouter Jukema, Masahiro Kanai, Keith L. Keene, Brett Kissela, Dawn Kleindorfer, Charles Kooperberg, Michiaki Kubo, Leslie A. Lange, Carl D. Langefeld, Claudia Langenberg, Lenore J. Launer, Jin‐Moo Lee, Robin Lemmens, Didier Leys, Cathryn M. Lewis, Wei‐Yu Lin, Arne G. Lindgren, Erik Lorentzen, Patrik K. E. Magnusson, Jane Maguire, Ani Manichaikul, Patrick F. McArdle, James F. Meschia, Braxton D. Mitchell, Thomas H. Mosley, Michael A. Nalls, Toshiharu Ninomiya, Martin O’Donnell, Bruce M. Psaty, Sara L. Pulit, Kristiina Rannikmäe, Alex P. Reiner, Kathryn M. Rexrode, Kenneth Rice, Stephen S. Rich, Paul M. Ridker, Natalia S. Rost, Peter M. Rothwell, Jerome I. Rotter, Tatjana Rundek, Ralph L. Sacco, Saori Sakaue, Michèle M. Sale
Nature Genetics. 20181,740 CitationsOPEN ACCESS
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C. Francioli, Androniki Menelaou, Sara L. Pulit, Clara C. Elbers, Wigard P. Kloosterman, Jessica van Setten, Isaäc J. Nijman, Ivo Renkens, Paul I. W. de Bakker, Freerk van Dijk, Pieter B. Neerincx, Patrick Deelen, Alexandros Kanterakis, Martijn Dijkstra, Heorhiy Byelas, K. Joeri van der Velde, Mathieu Platteel, Morris A. Swertz, Cisca Wijmenga, Pier Francesco Palamara, Itsik Pe’er, Kai Ye, Eric-Wubbo Lameijer, Matthijs H. Moed, Marian Beekman, Anton J. M. de Craen, H Eka D Suchiman, P. Eline Slagboom, Victor Guryev, Abdel Abdellaoui, Jouke‐Jan Hottenga, Mathijs Kattenberg, Gonneke Willemsen, Dorret I. Boomsma, Jin‐Moo Lee, Lennart C. Karssen, Najaf Amin, Fernando Rivadeneira, Aaron Isaacs, Albert Hofman, André G. Uitterlinden, Cornelia M. van Duijn, Mannis van Oven, Manfred Kayser, Martijn Vermaat, Jeroen F. J. Laros, Johan T. den Dunnen, David van Enckevort, Hailiang Mei, Mingkun Li, Mark Stoneking, Barbera D. C. van Schaik, Jan Bot, Tobias Marschall, Alexander Schönhuth, Jayne Y. Hehir‐Kwa, Robert E. Handsaker, Paz Polak, Mashaal Sohail, Dana Vuzman, Karol Estrada, Steven A. McCarroll, Shamil Sunyaev, Fereydoun Hormozdiari, Vyacheslav Koval, Carolina Medina‐Gómez, Ben Oostra, Jan H. Veldink, Leonard H. van den Berg, Steven J. Pitts, Shobha Potluri, Purnima Sundar, David R. Cox, Peter de Knijff, Qibin Li, Yingrui Li, Yuanping Du, Ruoyan Chen, Hongzhi Cao, Jun Wang, Ning Li, Sujie Cao, Jasper Bovenberg, Gert‐Jan B. van Ommen
Nature Genetics. 2014728 CitationsOPEN ACCESS
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
PARALS Registry, Wouter van Rheenen, SLALOM Group, SLAP Registry, NNIPPS Study Group, Aleksey Shatunov, Annelot M. Dekker, Russell L. McLaughlin, Frank P. Diekstra, Sara L. Pulit, Rick A. A. van der Spek, Urmo Võsa, Simone de Jong, Matthew R. Robinson, Jian Yang, Isabella Fogh, Perry Tc van Doormaal, Gijs Tazelaar, Max Koppers, Anna M. Blokhuis, William Sproviero, Ashley R Jones, Kevin P. Kenna, Kristel R. van Eijk, Oliver Harschnitz, Raymond D. Schellevis, William J. Brands, Jelena Medic, Androniki Menelaou, Alice Vajda, Nicola Ticozzi, Kuang Lin, Boris Rogelj, Katarina Vrabec, Metka Ravnik‐Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon Topp, Susanne Petri, Susanne Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A. Ophoff, Kim A. Staats, Martina Wiedau‐Pazos, Catherine Lomen‐Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, A. Nazlı Başak, Ceren Tunca, Hamid Hamzeiy, Yeşim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov‐Blagojevic, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean‐François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada
Nature Genetics. 2016639 CitationsOPEN ACCESS
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Dan E. Arking, DCCT/EDIC, Sara L. Pulit, Lia Crotti, Pim van der Harst, Patricia B. Munroe, Tamara T. Koopmann, Nona Sotoodehnia, Elizabeth J. Rossin, Michael P. Morley, Xinchen Wang, Andrew D. Johnson, Alicia Lundby, Daníel F. Guðbjartsson, Peter A. Noseworthy, Mark Eijgelsheim, Yuki Bradford, Kirill V. Tarasov, Marcus Dörr, Martina Müller‐Nurasyid, Annukka M. Lahtinen, Ilja M. Nolte, Albert V. Smith, Joshua C Bis, Aaron Isaacs, Stephen Newhouse, Daniel S. Evans, Wendy S. Post, Daryl Waggott, Leo‐Pekka Lyytikäinen, Andrew A. Hicks, Lewin Eisele, David Ellinghaus, Caroline Hayward, Pau Navarro, Sheila Ulivi, Toshiko Tanaka, David J. Tester, Stéphanie Chatel, Stefan Gustafsson, Meena Kumari, Richard Morris, Åsa Torinsson Naluai, Sandosh Padmanabhan, Alexander Kluttig, Bernhard Strohmer, Andrie G. Panayiotou, María Torres, Michael Knoflach, Jaroslav A. Hubáček, Kamil Slowikowski, Soumya Raychaudhuri, Runjun D. Kumar, Tamara B. Harris, Lenore J. Launer, Alan R. Shuldiner, Álvaro Alonso, Joel S. Bader, Georg Ehret, Hailiang Huang, W.H. Linda Kao, James B. Strait, Peter W. Macfarlane, Morris Brown, Mark J. Caulfield, Nilesh J. Samani, Florian Kronenberg, Johann Willeit, J. Gustav Smith, Karin Halina Greiser, Henriette E. Meyer zu Schwabedissen, Karl Werdan, Massimo Carella, Leopoldo Zelante, Susan R. Heckbert, Bruce M. Psaty, Jerome I. Rotter, Ivana Kolčić, Ozren Polašek, Alan F. Wright, Maura Griffin, Mark J. Daly, Davíð O. Arnar, Hilma Hólm, Unnur Þorsteinsdóttir, Joshua C. Denny, Dan M. Roden, Rebecca L. Zuvich, Valur Emilsson, Andrew Plump, Martin G. Larson, Christopher J. O’Donnell, Xiaoyan Yin, Marco Bobbo, Pio D’Adamo, Annamaria Iorio, Gianfranco Sinagra, Ángel Carracedo, Steven R. Cummings, Michael A. Nalls
Nature Genetics. 2014339 CitationsOPEN ACCESS
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study
Sara L. Pulit, Patrick F. McArdle, Quenna Wong, Rainer Malik, Katrina Gwinn, Sefanja Achterberg, Ale Algra, Philippe Amouyel, Christopher D. Anderson, Donna K. Arnett, Ethem Murat Arsava, John Attia, Hakan Ay, Traci M. Bartz, Thomas W.K. Battey, Oscar Benavente, Steve Bevan, Alessandro Biffi, Joshua C Bis, Susan H. Blanton, Giorgio B. Boncoraglio, Robert D. Brown, A I Burgess, Caty Carrera, Sherita N. Chapman Smith, Daniel I. Chasman, Ganesh Chauhan, Wei‐Min Chen, Yu‐Ching Cheng, Michael Chong, Lisa Cloonan, John W. Cole, Ioana Cotlarciuc, Carlos Cruchaga, Elisa Cuadrado‐Godia, Tushar Dave, Jesse Dawson, Stéphanie Debette, Hossein Delavaran, Cameron Dell, Martin Dichgans, Kimberly F. Doheny, Chuanhui Dong, David Duggan, Gunnar Engström, Michele K. Evans, Xavier Estivill Pallejà, Jessica D. Faul, Israel Fernández‐Cadenas, Myriam Fornage, Philippe M. Frossard, Karen L. Furie, Dale M. Gamble, Christian Gieger, Anne‐Katrin Giese, Eva Giralt‐Steinhauer, Hector M. González, An Goris, Sólveig Grétarsdóttir, Raji P. Grewal, Ulrike Grittner, Stefan Gustafsson, Buhm Han, Graeme J. Hankey, Laura Heitsch, Peter Higgins, Marc C. Hochberg, Elizabeth Holliday, Jemma C. Hopewell, Richard B. Horenstein, George Howard, M. Arfan Ikram, Andreea Ilinca, Erik Ingelsson, Marguerite R. Irvin, Rebecca D. Jackson, Christina Jern, Jordi Jiménez Conde, Julie A. Johnson, Katarina Jood, Muhammad S Kahn, Robert C. Kaplan, L. Jaap Kappelle, Sharon L.R. Kardia, Keith L. Keene, Brett Kissela, Dawn Kleindorfer, Simon A. Koblar, Daniel Labovitz, Lenore J. Launer, Cathy C. Laurie, Cecelia Laurie, Cue Hyunkyu Lee, Jin‐Moo Lee, Manuel Lehm, Robin Lemmens, Christopher Levi, Didier Leys, Arne Lindgren, W. T. Longstreth
The Lancet Neurology. 2015263 CitationsOPEN ACCESS

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