ScholarIQanswers from OpenAlex
Institute of Human Genetics
InstitutionResearch output, impact & collaborations
Institute of Human Genetics is a institution indexed in ScholarIQ from OpenAlex.
What is known about Institute of Human Genetics?
ScholarIQrecord summary
Institute of Human Genetics is a research organisation in Poznań, PL. OpenAlex records 7,659 works and 1,110,044 citations for it. 1,505 researchers list it as their most recent affiliation.
How many works does Institute of Human Genetics have?
ScholarIQindexed works
Institute of Human Genetics has 7,659 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Institute of Human Genetics have?
ScholarIQcitation count
Institute of Human Genetics has 1,110,044 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Institute of Human Genetics?
ScholarIQresearcher count
Institute of Human Genetics has 1,505 researchers in the ScholarIQ index.
What is the average h-index at Institute of Human Genetics?
ScholarIQavg h-index
Institute of Human Genetics has an average h-index of 125.5 in OpenAlex.
What is the ROR of Institute of Human Genetics?
ScholarIQror
The ROR for Institute of Human Genetics is on the source record.
What is the OpenAlex record for Institute of Human Genetics?
ScholarIQopenalex
The OpenAlex for Institute of Human Genetics is on the source record.
Who are the most-cited researchers behind Institute of Human Genetics?
ScholarIQtop researchers by citations
What are the most-cited papers on Institute of Human Genetics?
ScholarIQmost cited works
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew J. Farrer, Sarah Lincoln, Jennifer M. Kachergus, Mary Hulihan, Ryan J. Uitti, Donald B. Calne, A. Jon Stoessl, Ronald F. Pfeiffer, Nadja Patenge, Iria Carballo‐Carbajal, P. Vieregge, Friedrich Asmus, Bertram Müller‐Myhsok, Dennis W. Dickson, Thomas Meitinger, Tim M. Strom, Zbigniew K. Wszołek, Thomas Gasser
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Majid Nikpay, Alexandre F.R. Stewart, Ruth McPherson, Anuj Goel, Theodosios Kyriakou, Christopher Grace, Shapour Jalilzadeh, Hugh Watkins, Martin Farrall, Natalie R. van Zuydam, Cecilia M Lindgren, Andrew P Morris, Erik Ingelsson, Hong‐Hee Won, Andrew Bjonnes, Richa Saxena, Tõnu Esko, Sekar Kathiresan, Leanne M Hall, Christopher P. Nelson, Thomas R Webb, Nilesh J Samani, Christina Willenborg, Jeanette Erdmann, Inke R. König, Stavroula Kanoni, Kathleen Stirrups, Panos Deloukas, Danish Saleheen, Wei Zhao, Philippe Frossard, Asif Rasheed, Maria Samue, Alison H. Goodall, Jemma C. Hopewell, King Wai Lau, Rory Collins, Robert Clarke, Lingyao Zeng, Thorsten Kessler, Christian Hengstenberg, Heribert Schunkert, Christian Gieger, Thomas Meitinger, Annette Peters, Abbas Dehghan, André Uitterlinden, Paul S. de Vries, Oscar H Franco, Albert Hofman, Maris Alver, Evelin Mihailov, Natalia Pervjakova, Andres Metspalu, Markus Perola, Sebastian M. Armasu, Mariza de Andrade, Kirsi Auro, Emmi Tikkanen, Samuli Ripatti, Daniel I Chasman, Lynda M Rose, Julie E Buring, Paul M Ridker, Shufeng Chen, Xiangfeng Lu, Xueli Yang, Laiyuan Wang, Dongfeng Gu, Ian Ford, Nora Franceschini, Stefan Gustafsson, Jie Huang, John Danesh, Shih-Jen Hwang, L Adrienne Cupples, Christopher J O'Donnell, Yun Kyoung Kim, Bok-Ghee Han, Bong-Jo Kim, Marcus E Kleber, Winfried März, Yingchang Lu, Omri Gottesman, Erwin P Bottinger, Ruth J F Loos, Leo-Pekka Lyytikäinen, Pekka J. Karhunen, Terho Lehtimäki, Alanna C Morrison, Eric Boerwinkle, Liming Qu, Elias Salfati, Thomas Quertermous, Themistocles L. Assimes, Markus Scholz, Frank Beutner, Joachim Thiery, Albert V Smith, Vilmundur Gudnason
Genomewide Association Analysis of Coronary Artery Disease
Nilesh J. Samani, Jeanette Erdmann, Alistair S. Hall, Christian Hengstenberg, Massimo Mangino, Bjoern Mayer, Richard J. Dixon, Thomas Meitinger, Peter S. Braund, H. E. Wichmann, Jennifer H. Barrett, Inke R. König, Suzanne E. Stevens, Silke Szymczak, David‐Alexandre Trégouët, Mark M. Iles, Friedrich Pahlke, Helen Perlstein Pollard, Wolfgang Lieb, François Cambien, Marcus Fischer, Willem H. Ouwehand, Stefan Blankenberg, Anthony J. Balmforth, Andrea Baessler, Stephen G. Ball, Tim M. Strom, Ingrid Brænne, Christian Gieger, Panos Deloukas, Martin D. Tobin, Andreas Ziegler, John R. Thompson, Heribert Schunkert
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
Kenneth E. White, W. Evans, Jeffery L.H. O'Riordan, Marcy C. Speer, Michael J. Econs, Bettina Lorenz‐Depiereux, Monika Grabowski, Thomas Meitinger, Tim M. Strom
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
Fiona Francis, Steffen Hennig, Bernd Korn, Richard Reinhardt, P. de Jong, Albert J. Poustka, Hans Lehrach, Peter Rowe, J.N. Goulding, Tina C. Summerfield, R. Mountford, Andrew Read, Ewa Popowska, Ewa Pronicka, Kay E. Davies, J. L. H. O’Riordan, Michael J. Econs, Teresa Nesbitt, M. K. Drezner, C Oudet, Solange Pannetier, André Hanauer, Tim M. Strom, A Meindl, Bettina Lorenz, B. Cagnoli, Klaus Mohnike, Jan Murken, Thomas Meitinger
How much of the research on Institute of Human Genetics is open access?
ScholarIQopen access share
67%OPEN ACCESS