Prof. dr. Clyde Francks

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Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsEmail yang diverifikasi di mpi.nl
Anthony P MonacoUniversity Professor and President emeritus, Tufts UniversityEmail yang diverifikasi di tufts.edu
Amaia Carrión-CastilloBCBL - Basque Center on Cognition Brain and LanguageEmail yang diverifikasi di bcbl.eu
Xiang-Zhen Kong (孔祥祯)Zhejiang UniversityEmail yang diverifikasi di zju.edu.cn
Alex J. RichardsonSenior Research Associate, University of OxfordEmail yang diverifikasi di dpag.ox.ac.uk
Richard OlsonUniversity of ColoradoEmail yang diverifikasi di colorado.edu
Bruce F. PenningtonProfessor of PsychologyEmail yang diverifikasi di du.edu
John DeFriesFaculty Fellow, Institute for Behavioral GeneticsEmail yang diverifikasi di colorado.edu
Barbara FrankeProfessor of Molecular PsychiatryEmail yang diverifikasi di radboudumc.nl
Fabrice CrivelloGroupe d’Imagerie Neurofonctionnelle - Institut des Maladies Neurodégénératives - CNRS UMR 5293Email yang diverifikasi di u-bordeaux.fr
Silvia ParacchiniProfessor, University of St AndrewsEmail yang diverifikasi di st-andrews.ac.uk
Stan NelsonProfessor of Human Genetics, UCLAEmail yang diverifikasi di ucla.edu
Lon CardonChief Scientific Officer, BioMarin PharmaceuticalEmail yang diverifikasi di bmrn.com
Mazoyer BUniversité BordeauxEmail yang diverifikasi di u-bordeaux.fr
marc JoliotCEAEmail yang diverifikasi di u-bordeaux.fr
Thomas ScerriPostdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical ResearchEmail yang diverifikasi di wehi.edu.au
Martine HoogmanRadboud University Medical Center, NIjmegen, The NetherlandsEmail yang diverifikasi di radboudumc.nl
James T McCrackenUCLAEmail yang diverifikasi di mednet.ucla.edu
Else EisingLanguage and Genetics department, Max Planck Institute for PsycholinguisticsEmail yang diverifikasi di mpi.nl
Pierandrea MugliaGRiN Therapeutics, BelgiumEmail yang diverifikasi di grintherapeutics.com

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Prof. dr. Clyde Francks

Max Planck Institute & Radboud University Medical Center, Nijmegen, the Netherlands

Email yang diverifikasi di mpi.nl - Beranda

Brain Laterality/Asymmetry Psychiatric Genetics Genomics Neurobiology Neurodevelopment


Judul Urutkan menurut kutipan Urutkan menurut tahun Urutkan menurut judul	Dikutip oleh Dikutip oleh	Tahun
Large recurrent microdeletions associated with schizophrenia H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ... nature 455 (7210), 232-236, 2008	3722*	2008
Common genetic variants influence human subcortical brain structures DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ... Nature 520 (7546), 224-229, 2015	903	2015
The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020	746	2020
Meta-analysis and imputation refines the association of 15q25 with smoking quantity JZ Liu, F Tozzi, DM Waterworth, SG Pillai, P Muglia, L Middleton, ... Nature genetics 42 (5), 436-440, 2010	740	2010
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ... Brain imaging and behavior 8, 153-182, 2014	729	2014
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries PM Thompson, N Jahanshad, CRK Ching, LE Salminen, SI Thomopoulos, ... Translational psychiatry 10 (1), 100, 2020	587	2020
A genome-wide investigation of SNPs and CNVs in schizophrenia AC Need, D Ge, ME Weale, J Maia, S Feng, EL Heinzen, KV Shianna, ... PLoS genetics 5 (2), e1000373, 2009	576	2009
α-5/α-3 nicotinic receptor subunit alleles increase risk for heavy smoking W Berrettini, X Yuan, F Tozzi, K Song, C Francks, H Chilcoat, ... Molecular psychiatry 13 (4), 368-373, 2008	550	2008
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ... Molecular psychiatry 12 (12), 1129-1139, 2007	497	2007
A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium Human Molecular Genetics 7 (3), 571-578, 1998	495	1998
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function MS Artigas, DW Loth, LV Wain, SA Gharib, M Obeidat, W Tang, G Zhai, ... Nature genetics 43 (11), 1082-1090, 2011	483	2011
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder SE Fisher, C Francks, JT McCracken, JJ McGough, AJ Marlow, ... The American Journal of Human Genetics 70 (5), 1183-1196, 2002	446	2002
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia SE Fisher, C Francks, AJ Marlow, IL MacPhie, DF Newbury, LR Cardon, ... Nature genetics 30 (1), 86-91, 2002	396	2002
Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium XZ Kong, SR Mathias, T Guadalupe, ENIGMA Laterality Working Group, ... Proceedings of the National Academy of Sciences 115 (22), E5154-E5163, 2018	389	2018
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration S Paracchini, A Thomas, S Castro, C Lai, M Paramasivam, Y Wang, ... Human molecular genetics 15 (10), 1659-1666, 2006	372	2006
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry LJ Scott, P Muglia, XQ Kong, W Guan, M Flickinger, R Upmanyu, F Tozzi, ... Proceedings of the National Academy of Sciences 106 (18), 7501-7506, 2009	362	2009
On the other hand: including left-handers in cognitive neuroscience and neurogenetics RM Willems, LV der Haegen, SE Fisher, C Francks Nature reviews neuroscience 15 (3), 193-201, 2014	356	2014
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism SL Smalley, V Kustanovich, SL Minassian, JL Stone, MN Ogdie, ... The American Journal of Human Genetics 71 (4), 959-963, 2002	347	2002
Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts P Muglia, F Tozzi, NW Galwey, C Francks, R Upmanyu, XQ Kong, ... Molecular psychiatry 15 (6), 589-601, 2010	338	2010
A 77-kilobase region of chromosome 6p22. 2 is associated with dyslexia in families from the United Kingdom and from the United States C Francks, S Paracchini, SD Smith, AJ Richardson, TS Scerri, LR Cardon, ... The American Journal of Human Genetics 75 (6), 1046-1058, 2004	336	2004

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