Clyde Francks

Educated at: University of Oxford

Occupation: researcher

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Articles 95

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December 17, 2001

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

Simon Fisher, Clyde Francks, Anthony Monaco, Bruce F. Pennington
2001

Clyde Francks, Anthony Monaco
March 1, 2002

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

Simon Fisher, Anthony Monaco, Clyde Francks, Bruce F. Pennington
December 1, 2002

The genetic basis of dyslexia

Anthony Monaco, Clyde Francks
March 28, 2002

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

Simon Fisher, Anthony Monaco, Clyde Francks, Stanley F Nelson, James J McGough
August 14, 2002

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism

Simon Fisher, Anthony Monaco, Clyde Francks, Rita M. Cantor, Stanley F Nelson, James J McGough
January 3, 2002

A genomewide linkage screen for relative hand skill in sibling pairs

Simon Fisher, Anthony Monaco, Clyde Francks
February 2003

Confirmatory evidence for linkage of relative hand skill to 2p12-q11

Clyde Francks, Simon Fisher, Anthony Monaco
February 13, 2003

Use of multivariate linkage analysis for dissection of a complex cognitive trait

Simon Fisher, Stacey S. Cherny, Anthony Monaco, Clyde Francks
April 8, 2003

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

Simon Fisher, Anthony Monaco, Clyde Francks, Rita M. Cantor, Stanley F Nelson, James J McGough
November 1, 2003

Familial and genetic effects on motor coordination, laterality, and reading-related cognition

Clyde Francks, Simon Fisher, Kathleen C. Taylor, Anthony Monaco
October 28, 2003

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

Clyde Francks, Simon Fisher, Anthony Monaco
October 22, 2004

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

Silvia Paracchini, Simon Fisher, Anthony Monaco, Clyde Francks, Bruce F. Pennington
November 1, 2004

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

Silvia Paracchini, Simon Fisher, Clyde Francks, John Stein
August 3, 2004

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

Simon Fisher, Clyde Francks, Rita M. Cantor, Stanley F Nelson, James J McGough
May 1, 2004

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects

Simon Fisher, Clyde Francks, Anthony Monaco, Stanley F Nelson
October 1, 2005

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci

Simon Fisher, Clyde Francks, Anthony Monaco
May 15, 2006

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

Silvia Paracchini, Julian C Knight, Clyde Francks, Anthony Monaco, Andrew Copp, Richard Wade-Martins
May 3, 2006

Genes, cognition and dyslexia: learning to read the genome

Simon Fisher, Clyde Francks
January 1, 2006

Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

Simon Fisher, Clyde Francks, Rita M. Cantor, Stanley F Nelson
December 2007

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Matthias Groszer, Stefano Colella, Antonio Velayos-Baeza, Clyde Francks, Richard Wade-Martins, Kenneth Kendler, David St Clair, Hans-Jürgen Möller
April 2008

Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking

Vincent Mooser, Federica Tozzi, Clyde Francks
September 11, 2008

Large recurrent microdeletions associated with schizophrenia

Leena Peltonen-Palotie, Marcella Rietschel, Sven Cichon, Dan Rujescu, Kári Stefánsson, Augustine Kong, Hreinn Stefansson, Unnur Þorsteinsdóttir, Thomas Werge, Aslaug Jonasdottir, Srdjan Djurovic, Adalbjorg Jonasdottir, Engilbert Sigurdsson, Thordur Sigmundsson, Jes Olesen, Tiina Paunio, Alexander Georgi, Anna C. Need, Thorgeir E. Thorgeirsson, Clyde Francks, Daníel F. Guðbjartsson, Muriel Walshe, Elvira Bramon, Thomas F. Hansen, Henrik Ullum, Paul M. Matthews, Barbara Franke, Ole A. Andreassen, Lambertus Kiemeney, Markus M Nöthen, Robin Murray, Ingrid Melle, Hans-Jürgen Möller, Ina Giegling, Jouko Lönnqvist, Jaana Suvisaari, Jeffrey Gulcher, Richard Bruggeman, David St Clair, Olli P H Pietiläinen, Nelson A. Freimer, Roel Ophoff, Stacy Steinberg, Andrés Ingason, Annette M Hartmann, Brynja Magnusdottir, Ragnheidur Fossdal, Mirella Ruggeri, Sarah Tosato, Gillian M Fraser, Timi Toulopoulou, Kevin V Shianna, Pierandrea Muglia, Arnaldur Gylfason, Caroline Crombie, Jacobine E Buizer-Voskamp, Cătălina-Andreea Vasilescu, Thomas W Mühleisen, David Collier, Marta Di Forti, Asgeir Bjornsson, Bjarni V. Halldórsson, Asgeir Sigurdsson, David B. Goldstein, Dongliang Ge, Evangelos Vassos
July 1, 2008

Failure to replicate effect of Kibra on human memory in two large cohorts of European origin

Anna C. Need, Elizabeth T Cirulli, Clyde Francks, Hans-Jürgen Möller, Ina Giegling, Dan Rujescu, Pierandrea Muglia, Deborah Attix, Allen D. Roses
September 16, 2008

Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13.

Federica Tozzi, Clyde Francks, David St Clair
December 23, 2008

Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts

Federica Tozzi, Clyde Francks, Enrico Domenici, Florian Holsboer, Allen D. Roses
May 5, 2009

Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

Devin Absher, Huda Akil, Federica Tozzi, Clyde Francks, Keith Matthews, Margit Burmeister, Michael Boehnke, Peter McGuffin, James L. Kennedy, Allen D. Roses
February 6, 2009

A genome-wide investigation of SNPs and CNVs in schizophrenia

Anna C. Need, Giuseppe Rossi, Clyde Francks, Michael E. Weale, Massimo Gennarelli, Philip A Cola, Elizabeth M. C. Fisher, Hans-Jürgen Möller, Ina Giegling, Dan Rujescu, Karu Jayathilake, Herbert Y. Meltzer, David St Clair, Annette M Hartmann, L T Middleton, Erin L Heinzen, Gillian M Fraser, Pierandrea Muglia, Kevin V Shianna, Warren J Strittmatter, Cristian Bonvicini, Richard S E Keefe, Caroline Crombie, David B. Goldstein, Dongliang Ge, Jessica M Maia, Allen D. Roses
January 1, 2009

Understanding the genetics of behavioural and psychiatric traits will only be achieved through a realistic assessment of their complexity

Clyde Francks
September 29, 2009

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

Barbara Franke, Ole A. Andreassen, Clyde Francks, Engilbert Sigurdsson, Hreinn Stefansson, Elvira Bramon, Sven Cichon, Srdjan Djurovic, Thomas Werge, Marcella Rietschel, Kári Stefánsson, David St Clair, Markus M Nöthen, Torben Hansen, Jaana Suvisaari, Lambertus Kiemeney, Robin Murray, Hans-Jürgen Möller, Annamari Tuulio-Henriksson, Jacobine E Buizer-Voskamp, Abigail Fraser
May 2010

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

Peter Vollenweider, Inês Barroso, Henry Völzke, David Schlessinger, Alexander Teumer, Claudia Lamina, Igor Rudan, Veronique Vitart, Martin Farrall, Manuela Uda, Paul Scheet, Anna Dominiczak, Vincent Mooser, Dan Rujescu, Jack Satsangi, Miles Parkes, Kay-Tee Khaw, Heinz Erich Wichmann, Anne Farmer, Ozren Polašek, Caroline Hayward, Gérard Waeber, Jane Worthington, Antonio Terracciano, Lina Zgaga, Jonathan Marchini, Fabio Busonero, Marcus Ising, James F. Wilson, Federica Tozzi, Clyde Francks, Keith Matthews, Ivana Kolcic, Mark Caulfield, Wendy Thomson, Muredach P. Reilly, Alistair Scott Hall, Ulrich John, Anne Barton, Christopher G. Mathew, Nilesh Samani, Carl A Anderson, Nicholas J. Wareham, Ruth J. Loos, Ron Waksman, Patricia B Munroe, Lowell F Satler, Augusto D Pichard, Kenneth M Kent, Jaspal Kooner, Dawn Waterworth, Peter McGuffin, Harry Campbell, Daniel Rader, Andre Franke, David St Clair, Christopher W Knouff, Mary Susan Burnett, William H Matthai, Hakon Hakonarson, Philip J. Barter, Jennifer E Huffman, Sarah H Wild, Gonçalo Abecasis, John F Thompson, Ruth McPherson, L T Middleton, Pierandrea Muglia, Martin Preisig, Antero Kesäniemi, Rajesh Rawal, Xiangjun Xiao, Hans Jörgen Grabe, Michael Wittig, Norbert Dahmen, Alan F Wright, Jing Hua Zhao, John Campbell Chambers, Scott M. Grundy, James L. Kennedy
January 12, 2010

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

Ole A. Andreassen, Michael C O'Donovan, Marcella Rietschel, Sven Cichon, Srdjan Djurovic, Thomas Werge, Marta Di Forti, Clyde Francks, Muriel Walshe, Thomas F. Hansen, Markus M Nöthen, Robin Murray, Ingrid Melle, Leena Peltonen-Palotie, Hans-Jürgen Möller, Ina Giegling, Dan Rujescu, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio-Henriksson, Richard Bruggeman, Rita M. Cantor, David St Clair, Olli P H Pietiläinen, Roel Ophoff, Annette M Hartmann, Sarah Tosato, Eric Strengman, Pierandrea Muglia, Chiara Bonetto, Cătălina-Andreea Vasilescu, Thomas W Mühleisen, Andrés Ingason, Gesche Jürgens, Nick Craddock, David Collier, Evangelos Vassos

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