ScholarIQanswers from OpenAlex
Human Molecular Genetics
JournalCitation impact & published research
Human Molecular Genetics is a journal indexed in ScholarIQ from OpenAlex.
What is the OpenAlex record for Human Molecular Genetics?
ScholarIQopenalex
The OpenAlex for Human Molecular Genetics is on the source record.
What are the most-cited papers on Human Molecular Genetics?
ScholarIQmost cited works
DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific
Elmar W. Tobi, L. H. Lumey, Rudolf P. Talens, Dennis Kremer, Hein Putter, Aryeh D. Stein, P. Eline Slagboom, Bastiaan T. Heijmans
Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations
Patrick J. Pollard, J.-J. Brière, Neyaz Alam, Julian Barwell, Ella Barclay, Noel C. Wortham, Toby Hunt, Murray D. Mitchell, S. E. Olpin, Stuart J. Moat, Iain P. Hargreaves, Simon Heales, Yuen‐Li Chung, John R. Griffiths, A. Dalgleish, John A. McGrath, Michael J. Gleeson, S V Hodgson, Richard Poulsom, Pierre Rustin, Ian Tomlinson
Non-coding genetic variants in human disease: Figure 1.
Feng Zhang, James R. Lupski
A genome-wide scan for common alleles affecting risk for autism
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Jennifer Conroy, Tiago R. Magalhães, Catarina Correia, Brett S. Abrahams, N. Sykes, A. T. Pagnamenta, J.-P. de Almeida, Elena Bacchelli, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Sven Bölte, P. F. Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, A. R. Carson, Guillermo Casallo, Jillian P. Casey, Su H. Chu, Lynne Cochrane, Christina Corsello, E. L. Crawford, A. Crossett, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, James Gilbert, C. Gillberg, Joseph Glessner, Joel O. Goldberg, Jonathan Green, Stephen J. Guter, Håkon Håkonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, C. Kim, Sabine M. Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, A. C. Lionel, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Nadine Melhem, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, C. Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Joseph Piven, David J. Posey, Annemarie Poustka, Fritz Poustka
Disruption of the neurexin 1 gene is associated with schizophrenia
Dan Rujescu, Andrés Ingason, Sven Cichon, Olli Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurðsson, Thordur Sigmundsson, Hannes Pétursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Guðrún A. Jónsdóttir, Ómar Gústafsson, Ragnheiður Fossdal, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Folkmann Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, GROUP Investigators, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier