ScholarIQanswers from OpenAlex & ORCID
Hana Lango Allen
ResearcherPublications, citations & collaboration network
Hana Lango Allen is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Hana Lango Allen have?
ScholarIQindexed works
Hana Lango Allen has 106 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Hana Lango Allen have?
ScholarIQcitation count
Hana Lango Allen has 27,728 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Hana Lango Allen?
ScholarIQh-index
Hana Lango Allen has an h-index of 52 in OpenAlex.
What is the i10-index of Hana Lango Allen?
ScholarIQi10-index
Hana Lango Allen has an i10-index of 73 in OpenAlex.
What is the ORCID of Hana Lango Allen?
ScholarIQorcid
The ORCID for Hana Lango Allen is on the source record.
What is the OpenAlex record for Hana Lango Allen?
ScholarIQopenalex
The OpenAlex for Hana Lango Allen is on the source record.
What are the most-cited papers on Hana Lango Allen?
ScholarIQmost cited works
A Common Variant in the <i>FTO</i> Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity
Timothy M. Frayling, Nicholas J. Timpson, Michael N. Weedon, Eleftheria Zeggini, Rachel M. Freathy, Cecilia M. Lindgren, John R. B. Perry, Katherine S. Elliott, Hana Lango Allen, Nigel W. Rayner, Beverley M. Shields, Lorna W. Harries, Jeffrey C. Barrett, Sian Ellard, Christopher J. Groves, Bridget Knight, Ann‐Marie Patch, Andrew R. Ness, Shah Ebrahim, Debbie A. Lawlor, Susan M. Ring, Yoav Ben‐Shlomo, Marjo‐Riitta Järvelin, Ulla Sovio, Amanda J. Bennett, David Melzer, Luigi Ferrucci, Ruth J. F. Loos, Inês Barroso, Nicholas J. Wareham, Fredrik Karpe, Katharine R. Owen, Lon R. Cardon, Mark Walker, G. A. Hitman, Colin N. A. Palmer, Alex S. F. Doney, Andrew D. Morris, George Davey Smith, Andrew T. Hattersley, Mark I. McCarthy
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC, Elizabeth K. Speliotes, Cristen J. Willer, Sonja I. Berndt, Keri L. Monda, Guðmar Þorleifsson, Anne Jackson, Hana Lango Allen, Cecilia M. Lindgren, Jian’an Luan, Reedik Mägi, Joshua C. Randall, Sailaja Vedantam, Thomas W. Winkler, Lu Qi, Tsegaselassie Workalemahu, Iris M. Heid, Valgerður Steinthórsdóttir, Heather M. Stringham, Michael N. Weedon, Eleanor Wheeler, Andrew R. Wood, Teresa Ferreira, Robert J. Weyant, Ayellet V. Segrè, Karol Estrada, Liming Liang, James Nemesh, Ju-Hyun Park, Stefan Gustafsson, Tuomas O. Kilpeläinen, Jian Yang, Nabila Bouatia‐Naji, Tõnu Esko, Mary F. Feitosa, Zoltán Kutalik, Massimo Mangino, Soumya Raychaudhuri, André Scherag, Albert V. Smith, Ryan Welch, Wei Zhao, Katja K.H. Aben, Devin M. Absher, Najaf Amin, Anna Dixon, Eva Fisher, Nicole L. Glazer, Michael E. Goddard, Nancy L. Heard‐Costa, Volker Hoesel, Jouke‐Jan Hottenga, Åsa Johansson, Toby Johnson, Shamika Ketkar, Claudia Lamina, Shengxu Li, Miriam F. Moffatt, Richard H. Myers, Narisu Narisu, John R. B. Perry, Marjolein J. Peters, Michael Preuß, Samuli Ripatti, Fernando Rivadeneira, Camilla H. Sandholt, Laura J. Scott, Nicholas J. Timpson, Jonathan P. Tyrer, S. van Wingerden, Richard M. Watanabe, Charles C. White, Fredrik Wiklund, Cristina Barlassina, Daniel I. Chasman, Matthew N. Cooper, John‐Olov Jansson, Robert Lawrence, Niina Pellikka, Inga Prokopenko, Jianxin Shi, Elisabeth Thiering, Helene Alavere, Maria Teresa Sciarrone Alibrandi, Peter Almgren, Alice M. Arnold, Thor Aspelund, Larry D. Atwood, Beverley Balkau, Anthony J. Balmforth, Amanda J. Bennett, Yoav Ben‐Shlomo, Richard N. Bergman, Sven Bergmann, Heike Biebermann, Alexandra I. F. Blakemore, Tanja Boes, Lori L. Bonnycastle, Stefan R. Bornstein, Morris J Brown
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen, Karol Estrada, Guillaume Lettre, Sonja I. Berndt, Michael N. Weedon, Fernando Rivadeneira, Cristen J. Willer, Anne Jackson, Sailaja Vedantam, Soumya Raychaudhuri, Teresa Ferreira, Andrew R. Wood, Robert J. Weyant, Ayellet V. Segrè, Elizabeth K. Speliotes, Eleanor Wheeler, Nicole Soranzo, Ju‐Hyun Park, Jian Yang, Daníel F. Guðbjartsson, Nancy L. Heard‐Costa, Joshua C. Randall, Lu Qi, Albert V. Smith, Reedik Mägi, Tomi Pastinen, Liming Liang, Iris M. Heid, Jian’an Luan, Guðmar Þorleifsson, Thomas W. Winkler, Michael E. Goddard, Ken Sin Lo, Cameron D. Palmer, Tsegaselassie Workalemahu, Yurii S. Aulchenko, Åsa Johansson, M. Carola Zillikens, Mary F. Feitosa, Tõnu Esko, Toby Johnson, Shamika Ketkar, Peter Kraft, Massimo Mangino, Inga Prokopenko, Devin Absher, Eva Albrecht, Florian Ernst, Nicole L. Glazer, Caroline Hayward, Jouke‐Jan Hottenga, Kevin B. Jacobs, Joshua W. Knowles, Zoltán Kutalik, Keri L. Monda, Ozren Polašek, Michael Preuß, Nigel W. Rayner, Neil R. Robertson, Valgerður Steinthórsdóttir, Jonathan P. Tyrer, Benjamin F. Voight, Fredrik Wiklund, Jianfeng Xu, Wei Zhao, Dale R. Nyholt, Niina Pellikka, Markus Perola, John R. B. Perry, Ida Surakka, Mari‐Liis Tammesoo, Elizabeth L. Altmaier, Najaf Amin, Thor Aspelund, Tushar Bhangale, Gabrielle Boucher, Daniel I. Chasman, Constance Chen, Lachlan Coin, Matthew N. Cooper, Anna Dixon, Quince Gibson, Elin Grundberg, Ke Hao, Juhani Junttila, Lee M. Kaplan, Johannes Kettunen, Inke R. König, Tony Kwan, Robert Lawrence, Douglas F. Levinson, Mattias Lorentzon, Barbara McKnight, Andrew P. Morris, Martina Müller‐Nurasyid, Julius S. Ngwa, Shaun Purcell, Suzanne Rafelt, Rany M. Salem, Erika Salvi
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
Whole-genome sequencing of patients with rare diseases in a national health system
Ernest Turro, William J. Astle, Karyn Mégy, Stefan Gräf, Daniel Greene, Olga Shamardina, Hana Lango Allen, Alba Sanchis‐Juan, Mattia Frontini, Chantal Thys, Jonathan Stephens, Rutendo Mapeta, Oliver S. Burren, Kate Downes, Matthias Haimel, Salih Tuna, Sri V. V. Deevi, Timothy J. Aitman, David Bennett, Paul Calleja, Keren Carss, Mark J. Caulfield, Patrick F. Chinnery, Peter Dixon, Daniel P. Gale, Roger James, Ania Koziell, Michael A. Laffan, Adam P. Levine, Eamonn R. Maher, Hugh S. Markus, Joannella Morales, Nicholas W. Morrell, Andrew Mumford, Elizabeth Ormondroyd, Stuart Rankin, Augusto Rendon, Sylvia Richardson, Irene Roberts, Noémi Roy, Moin A. Saleem, Kenneth G. C. Smith, Hannah Stark, Rhea Tan, Andreas C. Themistocleous, Adrian J. Thrasher, Hugh Watkins, Andrew R. Webster, Martin R. Wilkins, Catherine Williamson, James Whitworth, Sean Humphray, David R. Bentley, NIHR BioResource for the 100,000 Genomes Project, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Paul Aurora, Christian Babbs, Chiara Bacchelli, Tamam Bakchoul, Siddharth Banka, Tadbir K. Bariana, Julian Barwell, Joana Batista, Helen Baxendale, Phil Beales, David Bennett, David R. Bentley, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme C. Black, Marta Bleda, Iulia Blesneac, Detlef Böckenhauer, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John R. Bradley, Eugene Bragin, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Andrew C. Browning, Michael J. Browning, Rachel Buchan