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Prof. dr. Clyde Francks
Prof. dr. Clyde Francks
Max Planck Institute & Radboud University Medical Center, Nijmegen, the Netherlands
Verified email at mpi.nl - Homepage
Title
Cited by
Cited by
Year
Large recurrent microdeletions associated with schizophrenia
H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ...
nature 455 (7210), 232-236, 2008
3614*2008
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivičres, ...
Nature 520 (7546), 224-229, 2015
8322015
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
7182010
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
6602014
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
5612020
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
5582009
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
5332008
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
5011998
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
4812007
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
4692011
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
4482020
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
4392002
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
3842002
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
3552009
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
3552006
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
3382002
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
3302004
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
3252014
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
3232018
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
3222010
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