ScholarIQanswers from OpenAlex & ORCID
Lukas Forer
ResearcherPublications, citations & collaboration network
Lukas Forer is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Lukas Forer have?
ScholarIQindexed works
Lukas Forer has 152 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Lukas Forer have?
ScholarIQcitation count
Lukas Forer has 20,243 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Lukas Forer?
ScholarIQh-index
Lukas Forer has an h-index of 38 in OpenAlex.
What is the i10-index of Lukas Forer?
ScholarIQi10-index
Lukas Forer has an i10-index of 77 in OpenAlex.
What is the ORCID of Lukas Forer?
ScholarIQorcid
The ORCID for Lukas Forer is on the source record.
What is the OpenAlex record for Lukas Forer?
ScholarIQopenalex
The OpenAlex for Lukas Forer is on the source record.
What are the most-cited papers on Lukas Forer?
ScholarIQmost cited works
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy, Yang Luo, Arthur Gilly, Jeffrey C. Barrett, Eleftheria Zeggini, Nicole Soranzo, Klaudia Walter, Carl A. Anderson, Richard Durbin, Sayantan Das, Hyun Min Kang, Christian Fuchsberger, Alan Kwong, Laura J. Scott, Sai Chen, Michael Boehnke, Abecasis Gb, Warren Kretzschmar, Anubha Mahajan, Mark I McCarthy, Jonathan Marchini, Olivier Delaneau, Andrew R Wood, Marcus A. Tuke, Timothy Frayling, Alexander Teumer, Matthias Nauck, Petr Danecek, Kevin Sharp, Carlo Sidore, Andrea Angius, Fabio Busonero, Francesco Cucca, Nicholas J. Timpson, Laura J. Corbin, George Davey Smith, Josine L. Min, Seppo Koskinen, V Salomaa, Scott Vrieze, He Zhang, Cristen J. Willer, Jan H. Veldink, Leonard H. van den Berg, Wouter van Rheenen, Annelot M. Dekker, Ulrike Peters, Tabitha A. Harrison, Charles Kooperberg, Carlos N. Pato, Michele T. Pato, Cornelia M. van Duijn, Christopher E. Gillies, Matthew G. Sampson, Ilaria Gandin, Massimiliano Cocca, Nicola Pirastu, Paolo Gasparini, Massimo Mezzavilla, Michela Traglia, Cinzia Sala, Daniela Toniolo, Dorrett Boomsma, Kari Branham, Gerome Breen, Chad M. Brummett, Ross M. Fraser, Harry Campbell, James F. Wilson, Andrew T. Chan, Matthias Kretzler, Emily Y. Chew, Francis S. Collins, George Dedoussis, Aliki‐Eleni Farmaki, Marcus Dörr, Uwe Völker, Luigi Ferrucci, Lukas Forer, Sebastian Schoenherr, Stacey Gabriel, Palotie A, David Altshuler, Shawn Levy, R Myers, Leif Groop, Andrew Hattersley, Oddgeir L. Holmen, Kristian Hveem, James Lee, M McGue, William Iacono, Thomas Meitinger, David Melzer, Karen L Mohlke, John B Vincent, Deborah Nickerson, Melvin McInnis, J Brent Richards, Kerrin Small
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Daniel Taliun, Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres, Sarah A. Gagliano Taliun, André Corvelo, Stephanie M. Gogarten, Hyun Min Kang, Achilleas Pitsillides, Jonathon LeFaive, Seung‐been Lee, Xiaowen Tian, Brian L. Browning, Sayantan Das, Anne‐Katrin Emde, Wayne E. Clarke, Douglas P. Loesch, Amol C. Shetty, Thomas W. Blackwell, Albert V. Smith, Quenna Wong, Xiaoming Liu, Matthew P. Conomos, Dean Bobo, François Aguet, Christine M. Albert, Álvaro Alonso, Kristin Ardlie, Dan E. Arking, Stella Aslibekyan, Paul L. Auer, John Barnard, R. Graham Barr, Lucas Barwick, Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Daniel I. Chasman, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie S. Emery, Celeste Eng, Diane Fatkin, Tasha E. Fingerlin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos
A saturated map of common genetic variants associated with human height
Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Saori Sakaue, Marielisa Graff, Anders Eliasen, Yunxuan Jiang, Sridharan Raghavan, Jenkai Miao, Joshua Arias, Sarah E. Graham, Ronen E. Mukamel, Cassandra N. Spracklen, Xianyong Yin, Shyh‐Huei Chen, Teresa Ferreira, Heather H Highland, Yingjie Ji, Tugce Karaderi, Kuang Lin, Kreete Lüll, Deborah E. Malden, Carolina Medina‐Gómez, Moara Machado, Amy Moore, Sina Rüeger, Xueling Sim, Scott Vrieze, Tarunveer S. Ahluwalia, Masato Akiyama, Matthew Allison, Marcus Alvarez, Mette K. Andersen, Alireza Ani, Vivek Appadurai, Liubov Arbeeva, Seema Bhaskar, Lawrence F. Bielak, Sailalitha Bollepalli, Lori L. Bonnycastle, Jette Bork‐Jensen, Jonathan P. Bradfield, Yuki Bradford, Peter S. Braund, Jennifer A. Brody, Kristoffer Sølvsten Burgdorf, Brian E. Cade, Hui Cai, Qiuyin Cai, Archie Campbell, Marisa Cañadas‐Garre, Eulalia Catamo, Jin Fang Chai, Xiaoran Chai, Li-Ching Chang, Yi‐Cheng Chang, Chien-Hsiun Chen, Alessandra Chesi, Seung Hoan Choi, Ren‐Hua Chung, Massimiliano Cocca, Maria Pina Concas, Christian Couture, Gabriel Cuéllar-Partida, Rebecca Danning, E. Warwick Daw, Frauke Degenhard, Graciela E. Delgado, Alessandro Delitala, Ayşe Demirkan, Xuan Deng, Poornima Devineni, Alexander Dietl, Maria Dimitriou, Latchezar Dimitrov, Rajkumar Dorajoo, Arif B. Ekici, Jorgen Engmann, Zammy Fairhurst-Hunter, Aliki‐Eleni Farmaki, Jessica D. Faul, Juan-Carlos Fernandez-Lopez, Lukas Forer, Margherita Francescatto, Sandra Freitag‐Wolf, Christian Fuchsberger, Tessel E. Galesloot, Yan Gao, Zishan Gao, Frank Geller, Olga Giannakopoulou, Franco Giulianini, Anette P. Gjesing, Anuj Goel, Scott D. Gordon, Mathias Gorski, Jakob Grove, Xiuqing Guo
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D. Beckmann, Guðmar Þorleifsson, Marco Belfiore, Sonia Bouquillon, Dominique Campion, Nicole de Leeuw, Bert B.A. de Vries, Tõnu Esko, Bridget A. Fernandez, Fernando Fernández‐Aranda, José Manuel Fernández‐Real, Mónica Gratacòs, Audrey Guilmatre, Juliane Hoyer, Marjo‐Riitta Järvelin, R. Frank Kooy, Ants Kurg, Cédric Le Caignec, Katrin Männik, Orah S. Platt, Damien Sanlaville, Mieke M. van Haelst, Sergi Villatoro Gomez, Faida Walha, Bai-Lin Wu, Yongguo Yu, Azzedine Aboura, Marie‐Claude Addor, Yves Alembik, Stylianos E. Antonarakis, Benoı̂t Arveiler, Magalie Barth, Nathalie Bednarek, Frédérique Béna, Sven Bergmann, Mylène Béri, Laura Bernardini, Bettina Blaumeiser, Dominique Bonneau, Armand Bottani, Odile Boute, Han G. Brunner, Dorothée Cailley, Patrick Callier, Jean Chiésa, Jacqueline Chrast, Lachlan Coin, Charles Coutton, Jean‐Marie Cuisset, J. Cuvellier, Albert David, Bénédicte de Fréminville, Bruno Delobel, Marie‐Ange Delrue, Bénédicte Demeer, Dominique Descamps, Gérard Didelot, Klaus Dieterich, Vittoria Disciglio, Martine Doco‐Fenzy, Séverine Drunat, Bénédicte Duban‐Bedu, Christèle Dubourg, Julia S. El-Sayed Moustafa, Paul Elliott, Brigitte H. W. Faas, Laurence Faivre, Anne Faudet, Florence Fellmann, Alessandra Ferrarini, Richard Fisher, Elisabeth Flori, Lukas Forer, Dominique Gaillard, Marion Gérard, Christian Gieger, Stefania Gimelli, Giorgio Gimelli, Hans J. Grabe, Agnès Guichet, Olivier Guillin, Anna‐Liisa Hartikainen, Delphine Héron, Loyse Hippolyte, Muriel Holder, Georg Homuth, Bertrand Isidor, Sylvie Jaillard, Zdenek Jaros, Susana Jiménez‐Múrcia, Géraldine Joly Helas