Prof. dr. Clyde Francks

Получаване на мой собствен потребителски профил

Позовавания

	Всички	От 2020
Позовавания	21897	8376
h-индекс	67	47
i10-индекс	111	93

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Публичен достъп

Преглед на всички

96 статии

0 статии

налични

неналични

Въз основа на изисквания при финансирането

Съавтори

Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsПотвърден имейл адрес: mpi.nl
Anthony P MonacoUniversity Professor and President emeritus, Tufts UniversityПотвърден имейл адрес: tufts.edu
Amaia Carrión-CastilloBCBL - Basque Center on Cognition Brain and LanguageПотвърден имейл адрес: bcbl.eu
Xiang-Zhen Kong (孔祥祯)Zhejiang UniversityПотвърден имейл адрес: zju.edu.cn
Alex J. RichardsonSenior Research Associate, University of OxfordПотвърден имейл адрес: dpag.ox.ac.uk
Richard OlsonUniversity of ColoradoПотвърден имейл адрес: colorado.edu
Bruce F. PenningtonProfessor of PsychologyПотвърден имейл адрес: du.edu
John DeFriesFaculty Fellow, Institute for Behavioral GeneticsПотвърден имейл адрес: colorado.edu
Barbara FrankeProfessor of Molecular PsychiatryПотвърден имейл адрес: radboudumc.nl
Fabrice CrivelloGroupe d’Imagerie Neurofonctionnelle - Institut des Maladies Neurodégénératives - CNRS UMR 5293Потвърден имейл адрес: u-bordeaux.fr
Silvia ParacchiniProfessor, University of St AndrewsПотвърден имейл адрес: st-andrews.ac.uk
Stan NelsonProfessor of Human Genetics, UCLAПотвърден имейл адрес: ucla.edu
Lon CardonChief Scientific Officer, BioMarin PharmaceuticalПотвърден имейл адрес: bmrn.com
Mazoyer BUniversité BordeauxПотвърден имейл адрес: u-bordeaux.fr
marc JoliotCEAПотвърден имейл адрес: u-bordeaux.fr
Thomas ScerriPostdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical ResearchПотвърден имейл адрес: wehi.edu.au
Martine HoogmanRadboud University Medical Center, NIjmegen, The NetherlandsПотвърден имейл адрес: radboudumc.nl
James T McCrackenUCLAПотвърден имейл адрес: mednet.ucla.edu
Else EisingLanguage and Genetics department, Max Planck Institute for PsycholinguisticsПотвърден имейл адрес: mpi.nl
Pierandrea MugliaGRiN Therapeutics, BelgiumПотвърден имейл адрес: grintherapeutics.com

Следене

Prof. dr. Clyde Francks

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

Потвърден имейл адрес: mpi.nl - Начална страница

Brain Laterality/Asymmetry Psychiatric Genetics Genomics Neurobiology Neurodevelopment


Заглавие Сортиране по цитати Сортиране по година Сортиране по заглавие	Позовавания Позовавания	Година
Large recurrent microdeletions associated with schizophrenia H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ... nature 455 (7210), 232-236, 2008	3718*	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
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	739	2010
The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020	735	2020
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	581	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	574	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	551	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	445	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	384	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	370	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	363	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	353	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	337	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	335	2004

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