Stylianos E. Antonarakis

Cited by

	All	Since 2019
Citations	145323	41312
h-index	165	77
i10-index	679	350

8000

4000

2000

6000

1985198619871988198919901991199219931994199519961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024390 466 529 613 635 740 972 960 1066 1083 1124 1130 1140 1436 1493 1773 2091 2260 2811 3116 3411 3574 3984 4364 4305 4666 4908 5357 6219 7043 7053 7172 6990 7178 7125 7403 7567 7295 6839 5035

Public access

View all

183 articles

8 articles

available

not available

Based on funding mandates

Co-authors

Hamish S ScottCenter of Cancer BiologyVerified email at sa.gov.au
Federico SantoniUniversity Hospital of LausanneVerified email at chuv.ch
Periklis MakrythanasisNational and Kapodistrian University of AthensVerified email at med.uoa.gr
Stuart OrkinVerified email at dfci.harvard.edu
Pärt PetersonProfessor of Molecular Immunology, University of Tartu, EstoniaVerified email at ut.ee
Roderic GuigoProfessor of Bioinformatics, Center for Genomic Regulation, Universitat Pompeu FabraVerified email at crg.cat
Melvin G McinnisProfessor of Psychiatry, University of MichiganVerified email at umich.edu
Sergey NikolaevGustave RoussyVerified email at gustaveroussy.fr
Dimitri AvramopoulosMcKusick Nathans Institute of Genetic Medicine, Johns Hopkins UniversityVerified email at jhmi.edu
Xavier Estivill MD PhDqGenomics (Quantitative Genomics Laboratories)Verified email at qgenomics.com
Jacques S BeckmannProf emeritus, UNILVerified email at unil.ch
Konstantin PopadinÉcole polytechnique fédérale de Lausanne, SwitzerlandVerified email at epfl.ch
Alan F. ScottAssoc Professor of Medicine, Institute of Genetic Medicine, Johns Hopkins UniversityVerified email at jhmi.edu
Stephen B MontgomeryProfessor, Pathology, Genetics and Biomedical Data Science, Stanford UniversityVerified email at stanford.edu
Roman ChrastEPFLVerified email at epfl.ch
Cédric HowaldHealth2030 Genome CenterVerified email at health2030.ch
Andrew J. SharpIcahn School of Medicine at Mount SinaiVerified email at mssm.edu
Dierssen MaraCenter for Genomic RegulationVerified email at crg.eu
Edward TuddenhamEmeritus Professor of Haemophilia, University College LondonVerified email at ucl.ac.uk
Philipp BucherGroup leader in Bioinformatics, EPFL and Swiss Institute of Bioinformatics, LausanneVerified email at epfl.ch

Stylianos E. Antonarakis

Professor of Genetic Medicine, University of Geneva Medical School

Verified email at unige.ch

Genetics Genomics Genetic/Genomic Medicine


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
An integrated encyclopedia of DNA elements in the human genome ENCODE Project Consortium Nature 489 (7414), 57, 2012	17058	2012
Initial sequencing and comparative analysis of the mouse genome European Bioinformatics Institute: Birney Ewan 3 Goldman Nick 3 Kasprzyk ... Nature 420 (6915), 520-562, 2002	8662	2002
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project Management Group Liefer Laura A. 51 Wetterstrand Kris A. 51 Good Peter J. 51 ... nature 447 (7146), 799-816, 2007	6075	2007
Landscape of transcription in human cells S Djebali, CA Davis, A Merkel, A Dobin, T Lassmann, A Mortazavi, ... Nature 489 (7414), 101-108, 2012	5672	2012
Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution Project management: Fulton Lucinda A. 1 Mardis Elaine R. 1 Wilson Richard K. 1 Nature 432 (7018), 695-716, 2004	2947	2004
The ENCODE (ENCyclopedia of DNA elements) project EA Feingold, PJ Good, MS Guyer, S Kamholz, L Liefer, K Wetterstrand, ... Science 306 (5696), 636-640, 2004	2426	2004
The complete sequence of a human genome S Nurk, S Koren, A Rhie, M Rautiainen, AV Bzikadze, A Mikheenko, ... Science 376 (6588), 44-53, 2022	2222	2022
Transcriptome and genome sequencing uncovers functional variation in humans T Lappalainen, M Sammeth, MR Friedländer, PAC ‘t Hoen, J Monlong, ... Nature 501 (7468), 506-511, 2013	2099	2013
Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion JT Dunnen, SE Antonarakis Human mutation 15 (1), 7-12, 2000	2043	2000
Positional cloning of the APECED gene K Nagamine, P Peterson, HS Scott, J Kudoh, S Minoshima, M Heino, ... Nature genetics 17 (4), 393-398, 1997	1653	1997
HGVS recommendations for the description of sequence variants: 2016 update JT Den Dunnen, R Dalgleish, DR Maglott, RK Hart, MS Greenblatt, ... Human mutation 37 (6), 564-569, 2016	1570	2016
The DNA sequence of human chromosome 21 M Hattori, A Fujiyama, TD Taylor, H Watanabe, T Yada, HS Park, ... Nature 405 (6784), 311-319, 2000	1551	2000
A whole-genome association study of major determinants for host control of HIV-1 J Fellay, KV Shianna, D Ge, S Colombo, B Ledergerber, M Weale, ... science 317 (5840), 944-947, 2007	1526	2007
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia CM Lewis, DF Levinson, LH Wise, LE DeLisi, RE Straub, I Hovatta, ... The American Journal of Human Genetics 73 (1), 34-48, 2003	1484	2003
Guidelines for investigating causality of sequence variants in human disease DG MacArthur, TA Manolio, DP Dimmock, HL Rehm, J Shendure, ... Nature 508 (7497), 469-476, 2014	1430	2014
Hypoxia-inducible nuclear factors bind to an enhancer element located 3'to the human erythropoietin gene. GL Semenza, MK Nejfelt, SM Chi, SE Antonarakis Proceedings of the National Academy of Sciences 88 (13), 5680-5684, 1991	1428	1991
The genome sequence of taurine cattle: a window to ruminant biology and evolution Bovine Genome Sequencing and Analysis Consortium, CG Elsik, ... Science 324 (5926), 522-528, 2009	1156	2009
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A D Lakich, HH Kazazian Jr, SE Antonarakis, J Gitschier Nature genetics 5 (3), 236-241, 1993	1152	1993
Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster SH Orkin, HH Kazazian Jr, SE Antonarakis, SC Goff, CD Boehm, ... Nature 296 (5858), 627-631, 1982	1134	1982
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene L Hendriks, CM van Duijn, P Cras, M Cruts, W Van Hul, F van Harskamp, ... Nature genetics 1 (3), 218-221, 1992	1124	1992

The system can't perform the operation now. Try again later.

Articles 1–20

Citations per year

Duplicate citations

Merged citations

Add co-authorsCo-authors

Follow

Cited by

Co-authors