ScholarIQanswers from OpenAlex & ORCID
Harald Grallert
ResearcherPublications, citations & collaboration network
Harald Grallert is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Harald Grallert have?
ScholarIQindexed works
Harald Grallert has 463 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Harald Grallert have?
ScholarIQcitation count
Harald Grallert has 64,323 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Harald Grallert?
ScholarIQh-index
Harald Grallert has an h-index of 95 in OpenAlex.
What is the i10-index of Harald Grallert?
ScholarIQi10-index
Harald Grallert has an i10-index of 258 in OpenAlex.
What is the ORCID of Harald Grallert?
ScholarIQorcid
The ORCID for Harald Grallert is on the source record.
What is the OpenAlex record for Harald Grallert?
ScholarIQopenalex
The OpenAlex for Harald Grallert is on the source record.
What are the most-cited papers on Harald Grallert?
ScholarIQmost cited works
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Eleftheria Zeggini, Laura J. Scott, Richa Saxena, Benjamin F. Voight, Jonathan Marchini, Tianle Hu, Paul IW de Bakker, Gonçalo R. Abecasis, Peter Almgren, Gitte Andersen, Kristin Ardlie, Kristina Bengtsson Boström, Richard N. Bergman, Lori L. Bonnycastle, Knut Borch‐Johnsen, Noël P. Burtt, Hong Chen, Peter S. Chines, Mark J. Daly, Parimal Deodhar, Chia-Jen Ding, Alex S. F. Doney, William L. Duren, Katherine S. Elliott, Michael R. Erdos, Timothy M. Frayling, Rachel M. Freathy, Lauren Gianniny, Harald Grallert, Niels Grarup, Christopher J. Groves, Candace Guiducci, Torben Hansen, Christian Herder, G. A. Hitman, Thomas E. Hughes, Bo Isomaa, Anne Jackson, Torben Jørgensen, Augustine Kong, Kari Kubalanza, Finny G. Kuruvilla, Johanna Kuusisto, Claudia Langenberg, Hana Lango Allen, Torsten Lauritzen, Yun Li, Cecilia M. Lindgren, Valeriya Lyssenko, Amanda F. Marvelle, Christa Meisinger, Kristian Midthjell, Karen L. Mohlke, Mario A. Morken, Andrew D. Morris, Narisu Narisu, Peter M. Nilsson, Katharine R. Owen, Colin NA Palmer, Felicity Payne, John R. B. Perry, Elin Pettersen, Carl G. P. Platou, Inga Prokopenko, Lu Qi, Qin Li, Nigel W. Rayner, Matthew G. Rees, Jeffrey J. Roix, Anelli Sandbæk, Beverley M. Shields, Marketa Sjögren, Valgerður Steinthórsdóttir, Heather M. Stringham, Amy J. Swift, Gudmar Thorleifsson, Unnur Þorsteinsdóttir, Nicholas J. Timpson, Tiinamaija Tuomi, Jaakko Tuomilehto, Mark Walker, Richard M. Watanabe, Michael N. Weedon, Cristen J. Willer, Thomas Illig, Kristian Hveem, Frank B. Hu, Markku Laakso, Kāri Stefánsson, Oluf Pedersen, Nicholas J. Wareham, Inês Barroso, Andrew T. Hattersley, Francis S. Collins, Leif Groop, Mark I. McCarthy, Michael Boehnke, David Altshuler
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
The MAGIC investigators, Benjamin F. Voight, Laura J. Scott, Valgerður Steinthórsdóttir, Andrew P. Morris, Christian Dina, Ryan Welch, Eleftheria Zeggini, Cornelia Huth, Yurii S. Aulchenko, Guðmar Þorleifsson, Laura McCulloch, Teresa Ferreira, Harald Grallert, Najaf Amin, Guanming Wu, Cristen J. Willer, Soumya Raychaudhuri, Steve McCarroll, Claudia Langenberg, Oliver Hofmann, Josée Dupuis, Lu Qi, Ayellet V. Segrè, Mandy van Hoek, Pau Navarro, Kristin Ardlie, Beverley Balkau, Rafn Benediktsson, Amanda J. Bennett, Roza Blagieva, Eric Boerwinkle, Lori L. Bonnycastle, Kristina Bengtsson Boström, Bert Bravenboer, Suzannah Bumpstead, Noisël P Burtt, G. Charpentier, Peter S. Chines, Marilyn C. Cornelis, David Couper, Gabe Crawford, Alex S. F. Doney, Katherine S. Elliott, Amanda L. Elliott, Michael R. Erdos, Caroline S. Fox, Christopher S. Franklin, Martha Ganser, Christian Gieger, Niels Grarup, Todd J. Green, Simon J. Griffin, Christopher J. Groves, Candace Guiducci, Samy Hadjadj, Neelam Hassanali, Christian Herder, Bo Isomaa, Anne Jackson, Paul R V Johnson, Torben Jørgensen, Wen H. Kao, Norman Klopp, Augustine Kong, Peter Kraft, Johanna Kuusisto, Torsten Lauritzen, Man Li, Aloysius G. Lieverse, Cecilia M. Lindgren, Valeriya Lyssenko, Michel Marre, Thomas Meitinger, Kristian Midthjell, Mario A. Morken, Narisu Narisu, Peter M. Nilsson, Katharine R. Owen, Felicity Payne, John R. B. Perry, Ann-Kristin Petersen, Carl G. P. Platou, Christine Proença, Inga Prokopenko, Wolfgang Rathmann, Nigel W. Rayner, Neil R. Robertson, Ghislain Rocheleau, Michael Roden, Michael Sampson, Richa Saxena, Beverley M. Shields, Peter Shrader, Gunnar Sigurðsson, Thomas Sparsø, Klaus Straßburger, Heather M. Stringham, Qi Sun, Amy J. Swift
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra, Marjolein J. Peters, Tõnu Esko, Hanieh Yaghootkar, Claudia Schurmann, Johannes Kettunen, Mark Christiansen, Benjamin P. Fairfax, Katharina Schramm, Joseph E. Powell, Alexandra Zhernakova, Daria V. Zhernakova, Jan H. Veldink, Leonard H. van den Berg, Juha Karjalainen, Sebo Withoff, André G. Uitterlinden, Albert Hofman, Fernando Rivadeneira, Peter A.C. ’t Hoen, Eva Reinmaa, Krista Fischer, Mari Nelis, Lili Milani, David Melzer, Luigi Ferrucci, Andrew Singleton, Dena Hernández, Michael A. Nalls, Georg Homuth, Matthias Nauck, Dörte Radke, Uwe Völker, Markus Perola, Veikko Salomaa, Jennifer A. Brody, Astrid M. Suchy‐Dicey, Sina A. Gharib, Daniel A. Enquobahrie, Thomas Lumley, Grant W. Montgomery, Seiko Makino, Holger Prokisch, Christian Herder, Michael Roden, Harald Grallert, Thomas Meitinger, Konstantin Strauch, Yang Li, Ritsert C. Jansen, Peter M. Visscher, Julian C. Knight, Bruce M. Psaty, Samuli Ripatti, Alexander Teumer, Timothy M. Frayling, Andres Metspalu, Joyce B. J. van Meurs, Lude Franke
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato, Andreas Dufke, Kirsten Cremer, Maja Hempel, Denise Horn, Juliane Hoyer, Pascal Joset, Albrecht Röpke, Ute Moog, Angelika Rieß, Christian T. Thiel, Andreas Tzschach, Antje Wiesener, Eva Wohlleber, Christiane Zweier, Arif B. Ekici, Alexander M. Zink, Andreas Rump, Christa Meisinger, Harald Grallert, Heinrich Sticht, Annette Schenck, Hartmut Engels, Gudrun Rappold, Evelin Schröck, Peter Wieacker, Olaf Rieß, Thomas Meitinger, André Reis, Tim M. Strom
Connecting genetic risk to disease end points through the human blood plasma proteome
Karsten Suhre, Matthias Arnold, Aditya Bhagwat, Richard Cotton, Rudolf Engelke, Johannes Raffler, Hina Sarwath, Gaurav Thareja, Annika Wahl, Robert Kirk DeLisle, Larry Gold, Marija Pezer, Gordan Lauc, Mohammed A. El-Din Selim, Dennis O. Mook‐Kanamori, Eman Al‐Dous, Yasmin A. Mohamoud, Joel A. Malek, Konstantin Strauch, Harald Grallert, Annette Peters, Gabi Kastenmüller, Christian Gieger, Johannes Graumann