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Lon Cardon

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Publications

TOP 3
Manolio Teri A; Collins Francis S; Cox Nancy J; Goldstein David B; Hindorff Lucia A; Hunter David J; McCarthy Mark I; Ramos Erin M; Cardon Lon R; Chakravarti Aravinda; Cho Judy H; Guttmacher Alan E; Kong Augustine; Kruglyak Leonid; Mardis Elaine; Rotimi Charles N; Slatkin Montgomery; Valle David; Whittemore Alice S; Boehnke Michael; Clark Andrew G; Eichler Evan E; Gibson Greg; Haines Jonathan L; Mackay Trudy F C; McCarroll Steven A; Visscher Peter M
Finding the missing heritability of complex diseases.
Brocklebank D; Gayán J; Andresen J M; Roberts S A; Young A B; Snodgrass S R; Penney J B; Ramos-Arroyo M A; Cha J J; Rosas H D; Hersch S M; Feigin A; Cherny S S; Wexler N S; Housman D E; Cardon L R;
Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications.
Lawrence Robert; Day-Williams Aaron G; Mott Richard; Broxholme John; Cardon Lon R; Zeggini Eleftheria
GLIDERS--a web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs.

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All Publications

2009: Manolio Teri A; Collins Francis S; Cox Nancy J; Goldstein David B; Hindorff Lucia A; Hunter David J; McCarthy Mark I; Ramos Erin M; Cardon Lon R; Chakravarti Aravinda; Cho Judy H; Guttmacher Alan E; Kong Augustine; Kruglyak Leonid; Mardis Elaine; Rotimi Charles N; Slatkin Montgomery; Valle David; Whittemore Alice S; Boehnke Michael; Clark Andrew G; Eichler Evan E; Gibson Greg; Haines Jonathan L; Mackay Trudy F C; McCarroll Steven A; Visscher Peter M
Finding the missing heritability of complex diseases.
Nature 2009;461(7265):747-53.
2009: Brocklebank D; Gayán J; Andresen J M; Roberts S A; Young A B; Snodgrass S R; Penney J B; Ramos-Arroyo M A; Cha J J; Rosas H D; Hersch S M; Feigin A; Cherny S S; Wexler N S; Housman D E; Cardon L R;
Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(3):425-9.
2009: Lawrence Robert; Day-Williams Aaron G; Mott Richard; Broxholme John; Cardon Lon R; Zeggini Eleftheria
GLIDERS--a web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs.
BMC bioinformatics 2009;10():367.
2009: Pettersson Fredrik H; Anderson Carl A; Clarke Geraldine M; Barrett Jeffrey C; Cardon Lon R; Morris Andrew P; Zondervan Krina T
Marker selection for genetic case-control association studies.
Nature protocols 2009;4(5):743-52.
2008: Heath Simon C; Gut Ivo G; Brennan Paul; McKay James D; Bencko Vladimir; Fabianova Eleonora; Foretova Lenka; Georges Michael; Janout Vladimir; Kabesch Michael; Krokan Hans E; Elvestad Maiken B; Lissowska Jolanta; Mates Dana; Rudnai Peter; Skorpen Frank; Schreiber Stefan; Soria José M; Syvänen Ann-Christine; Meneton Pierre; Herçberg Serge; Galan Pilar; Szeszenia-Dabrowska Neonilia; Zaridze David; Génin Emmanuel; Cardon Lon R; Lathrop Mark
Investigation of the fine structure of European populations with applications to disease association studies.
European journal of human genetics : EJHG 2008;16(12):1413-29.
2008: Anderson Carl A; Pettersson Fredrik H; Barrett Jeffrey C; Zhuang Joanna J; Ragoussis Jiannis; Cardon Lon R; Morris Andrew P
Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms.
American journal of human genetics 2008;83(1):112-9.
2008: Gayán Javier; Brocklebank Denise; Andresen J Michael; Alkorta-Aranburu Gorka; Zameel Cader M; Roberts Simone A; Cherny Stacey S; Wexler Nancy S; Cardon Lon R; Housman David E
Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds.
Genetic epidemiology 2008;32(5):445-53.
2008: Evans David M; Barrett Jeffrey C; Cardon Lon R
To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?
European journal of human genetics : EJHG 2008;16(6):718-23.
2008: Dong Linda M; Potter John D; White Emily; Ulrich Cornelia M; Cardon Lon R; Peters Ulrike
Genetic susceptibility to cancer: the role of polymorphisms in candidate genes.
JAMA : the journal of the American Medical Association 2008;299(20):2423-36.
2008: McCarthy Mark I; Abecasis Gonçalo R; Cardon Lon R; Goldstein David B; Little Julian; Ioannidis John P A; Hirschhorn Joel N
Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
Nature reviews. Genetics 2008;9(5):356-69.
2008: Ke Xiayi; Taylor Martin S; Cardon Lon R
Singleton SNPs in the human genome and implications for genome-wide association studies.
European journal of human genetics : EJHG 2008;16(4):506-15.
2008: Pettersson Fredrik; Morris Andrew P; Barnes Michael R; Cardon Lon R
Goldsurfer2 (Gs2): a comprehensive tool for the analysis and visualization of genome wide association studies.
BMC bioinformatics 2008;9():138.
2007: Clarke Geraldine M; Carter Kim W; Palmer Lyle J; Morris Andrew P; Cardon Lon R
Fine mapping versus replication in whole-genome association studies.
American journal of human genetics 2007;81(5):995-1005.
2007: Cummings J R Fraser; Ahmad Tariq; Geremia Alessandra; Beckly John; Cooney Rachel; Hancock Laura; Pathan Saad; Guo Changcun; Cardon Lon R; Jewell Derek P
Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype.
Inflammatory bowel diseases 2007;13(9):1063-8.
2007: Cummings J R Fraser; Cooney Rachel; Pathan Saad; Anderson Carl A; Barrett Jeffrey C; Beckly John; Geremia Alessandra; Hancock Laura; Guo Changcun; Ahmad Tariq; Cardon Lon R; Jewell Derek P
Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene.
Inflammatory bowel diseases 2007;13(8):941-6.
2007: van Heel David A; Franke Lude; Hunt Karen A; Gwilliam Rhian; Zhernakova Alexandra; Inouye Mike; Wapenaar Martin C; Barnardo Martin C N M; Bethel Graeme; Holmes Geoffrey K T; Feighery Con; Jewell Derek; Kelleher Dermot; Kumar Parveen; Travis Simon; Walters Julian R F; Sanders David S; Howdle Peter; Swift Jill; Playford Raymond J; McLaren William M; Mearin M Luisa; Mulder Chris J; McManus Ross; McGinnis Ralph; Cardon Lon R; Deloukas Panos; Wijmenga Cisca
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
Nature genetics 2007;39(7):827-9.
2007: Zeggini Eleftheria; Weedon Michael N; Lindgren Cecilia M; Frayling Timothy M; Elliott Katherine S; Lango Hana; Timpson Nicholas J; Perry John R B; Rayner Nigel W; Freathy Rachel M; Barrett Jeffrey C; Shields Beverley; Morris Andrew P; Ellard Sian; Groves Christopher J; Harries Lorna W; Marchini Jonathan L; Owen Katharine R; Knight Beatrice; Cardon Lon R; Walker Mark; Hitman Graham A; Morris Andrew D; Doney Alex S F; McCarthy Mark I; Hattersley Andrew T
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
Science (New York, N.Y.) 2007;316(5829):1336-41.
2007: Andresen J Michael; Gayán Javier; Djoussé Luc; Roberts Simone; Brocklebank Denise; Cherny Stacey S; Cardon Lon R; Gusella James F; MacDonald Marcy E; Myers Richard H; Housman David E; Wexler Nancy S
The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset.
Annals of human genetics 2007;71(Pt 3):295-301.
2007: Zondervan Krina T; Treloar Susan A; Lin Jianghai; Weeks Daniel E; Nyholt Dale R; Mangion Jon; MacKay Ian J; Cardon Lon R; Martin Nicholas G; Kennedy Stephen H; Montgomery Grant W
Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
Human reproduction (Oxford, England) 2007;22(3):717-28.
2007: Andresen J M; Gayán J; Cherny S S; Brocklebank D; Alkorta-Aranburu G; Addis E A; Cardon L R; Housman D E; Wexler N S
Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds.
Journal of medical genetics 2007;44(1):44-50.
2007: Zondervan Krina T; Cardon Lon R
Designing candidate gene and genome-wide case-control association studies.
Nature protocols 2007;2(10):2492-501.
2006: Cardon Lon R
Genetics. Delivering new disease genes.
Science (New York, N.Y.) 2006;314(5804):1403-5.
2006: Evans D M; Morris A P; Cardon L R; Sham P C
A note on the power to detect transmission distortion in parent-child trios via the transmission disequilibrium test.
Behavior genetics 2006;36(6):947-50.
2006: McGovern Dermot P B; Butler Helen; Ahmad Tariq; Paolucci Marta; van Heel David A; Negoro Kenichi; Hysi Pirro; Ragoussis Jiannis; Travis Simon P L; Cardon Lon R; Jewell Derek P
TUCAN (CARD8) genetic variants and inflammatory bowel disease.
Gastroenterology 2006;131(4):1190-6.
2006: Gregersen Jon W; Kranc Kamil R; Ke Xiayi; Svendsen Pia; Madsen Lars S; Thomsen Allan Randrup; Cardon Lon R; Bell John I; Fugger Lars
Functional epistasis on a common MHC haplotype associated with multiple sclerosis.
Nature 2006;443(7111):574-7.
2006: Evans David M; Marchini Jonathan; Morris Andrew P; Cardon Lon R
Two-stage two-locus models in genome-wide association.
PLoS genetics 2006;2(9):e157.
2006: Yoo Yeon-Kyeong; Ke Xiayi; Hong Sungwoo; Jang Hye-Yoon; Park Kyunghee; Kim Sook; Ahn TaeJin; Lee Yeun-Du; Song Okryeol; Rho Na-Young; Lee Moon Sue; Lee Yeon-Su; Kim Jaeheup; Kim Young J; Yang Jun-Mo; Song Kyuyoung; Kimm Kyuchan; Weir Bruce; Cardon Lon R; Lee Jong-Eun; Hwang Jung-Joo
Fine-scale map of encyclopedia of DNA elements regions in the Korean population.
Genetics 2006;174(1):491-7.
2006: Evans David M; Cardon Lon R
Genome-wide association: a promising start to a long race.
Trends in genetics : TIG 2006;22(7):350-4.
2006: Barrett Jeffrey C; Cardon Lon R
Evaluating coverage of genome-wide association studies.
Nature genetics 2006;38(6):659-62.
2006: González-Neira Anna; Ke Xiayi; Lao Oscar; Calafell Francesc; Navarro Arcadi; Comas David; Cann Howard; Bumpstead Suzannah; Ghori Jilur; Hunt Sarah; Deloukas Panos; Dunham Ian; Cardon Lon R; Bertranpetit Jaume
The portability of tagSNPs across populations: a worldwide survey.
Genome research 2006;16(3):323-30.
2005: Zeggini Eleftheria; Rayner William; Morris Andrew P; Hattersley Andrew T; Walker Mark; Hitman Graham A; Deloukas Panos; Cardon Lon R; McCarthy Mark I
An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets.
Nature genetics 2005;37(12):1320-2.
2005: Clarke Geraldine M; Cardon Lon R
Disentangling linkage disequilibrium and linkage from dense single-nucleotide polymorphism trio data.
Genetics 2005;171(4):2085-95.
2005: Lawrence Robert; Evans David M; Morris Andrew P; Ke Xiayi; Hunt Sarah; Paolucci Marta; Ragoussis Jiannis; Deloukas Panos; Bentley David; Cardon Lon R
Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants.
Genome research 2005;15(11):1503-10.
2005: Weir Bruce S; Cardon Lon R; Anderson Amy D; Nielsen Dahlia M; Hill William G
Measures of human population structure show heterogeneity among genomic regions.
Genome research 2005;15(11):1468-76.
2005: Palmer Lyle J; Cardon Lon R
Shaking the tree: mapping complex disease genes with linkage disequilibrium.
Lancet 2005;366(9492):1223-34.
2005: Gayán J; Willcutt E G; Fisher S E; Francks C; Cardon L R; Olson R K; Pennington B F; Smith S D; Monaco A P; DeFries J C
Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.
Journal of child psychology and psychiatry, and allied disciplines 2005;46(10):1045-56.
2005: Ke Xiayi; Miretti Marcos M; Broxholme John; Hunt Sarah; Beck Stephan; Bentley David R; Deloukas Panos; Cardon Lon R
A comparison of tagging methods and their tagging space.
Human molecular genetics 2005;14(18):2757-67.
2005: Lawrence Robert W; Evans David M; Cardon Lon R
Prospects and pitfalls in whole genome association studies.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2005;360(1460):1589-95.
2005: Marchini Jonathan; Donnelly Peter; Cardon Lon R
Genome-wide strategies for detecting multiple loci that influence complex diseases.
Nature genetics 2005;37(4):413-7.
2005: Miretti Marcos M; Walsh Emily C; Ke Xiayi; Delgado Marcos; Griffiths Mark; Hunt Sarah; Morrison Jonathan; Whittaker Pamela; Lander Eric S; Cardon Lon R; Bentley David R; Rioux John D; Beck Stephan; Deloukas Panos
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.
American journal of human genetics 2005;76(4):634-46.
2005: Evans David M; Cardon Lon R
A comparison of linkage disequilibrium patterns and estimated population recombination rates across multiple populations.
American journal of human genetics 2005;76(4):681-7.
2005: Zondervan Krina T; Cardon Lon R; Kennedy Stephen H; Martin Nicholas G; Treloar Susan A
Multivariate genetic analysis of chronic pelvic pain and associated phenotypes.
Behavior genetics 2005;35(2):177-88.
2005: Wiltshire Steven; Morris Andrew P; McCarthy Mark I; Cardon Lon R
How useful is the fine-scale mapping of complex trait linkage peaks? Evaluating the impact of additional microsatellite genotyping on the posterior probability of linkage.
Genetic epidemiology 2005;28(1):1-10.
2004: Evans David M; Cardon Lon R; Morris Andrew P
Genotype prediction using a dense map of SNPs.
Genetic epidemiology 2004;27(4):375-84.
2004: Weir B S; Hill W G; Cardon L R;
Allelic association patterns for a dense SNP map.
Genetic epidemiology 2004;27(4):442-50.
2004: Francks Clyde; Paracchini Silvia; Smith Shelley D; Richardson Alex J; Scerri Tom S; Cardon Lon R; Marlow Angela J; MacPhie I Laurence; Walter Janet; Pennington Bruce F; Fisher Simon E; Olson Richard K; DeFries John C; Stein John F; Monaco Anthony P
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
American journal of human genetics 2004;75(6):1046-58.
2004: Ke Xiayi; Durrant Caroline; Morris Andrew P; Hunt Sarah; Bentley David R; Deloukas Panos; Cardon Lon R
Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.
Human molecular genetics 2004;13(21):2557-65.
2004: Pettersson Fredrik; Jonsson Oskar; Cardon Lon R
GOLDsurfer: three dimensional display of linkage disequilibrium.
Bioinformatics (Oxford, England) 2004;20(17):3241-3.
2004: Evans David M; Cardon Lon R
Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps.
American journal of human genetics 2004;75(4):687-92.
2004: Timms Andrew E; Crane Alison M; Sims Anne-Marie; Cordell Heather J; Bradbury Linda A; Abbott Aaron; Coyne Mark R E; Beynon Owen; Herzberg Ibi; Duff Gordon W; Calin Andrei; Cardon Lon R; Wordsworth B Paul; Brown Matthew A
The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis.
American journal of human genetics 2004;75(4):587-95.
2004: Durrant Caroline; Zondervan Krina T; Cardon Lon R; Hunt Sarah; Deloukas Panos; Morris Andrew P
Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.
American journal of human genetics 2004;75(1):35-43.
2004: Marchini Jonathan; Cardon Lon R; Phillips Michael S; Donnelly Peter
The effects of human population structure on large genetic association studies.
Nature genetics 2004;36(5):512-7.
2004: Wiltshire Steven; Frayling Timothy M; Groves Christopher J; Levy Jonathan C; Hitman Graham A; Sampson Mike; Walker Mark; Menzel Stephan; Hattersley Andrew T; Cardon Lon R; McCarthy Mark I
Evidence from a large U.K. family collection that genes influencing age of onset of type 2 diabetes map to chromosome 12p and to the MODY3/NIDDM2 locus on 12q24.
Diabetes 2004;53(3):855-60.
2004: Ke Xiayi; Hunt Sarah; Tapper William; Lawrence Robert; Stavrides George; Ghori Jilur; Whittaker Pamela; Collins Andrew; Morris Andrew P; Bentley David; Cardon Lon R; Deloukas Panos
The impact of SNP density on fine-scale patterns of linkage disequilibrium.
Human molecular genetics 2004;13(6):577-88.
2004: Zondervan Krina T; Weeks Daniel E; Colman Ricki; Cardon Lon R; Hadfield Ruth; Schleffler Joan; Trainor Amanda Goudy; Coe Christopher L; Kemnitz Joseph W; Kennedy Stephen H
Familial aggregation of endometriosis in a large pedigree of rhesus macaques.
Human reproduction (Oxford, England) 2004;19(2):448-55.
2004: Zondervan Krina T; Cardon Lon R
The complex interplay among factors that influence allelic association.
Nature reviews. Genetics 2004;5(2):89-100.
2003: van Heel David A; Dechairo Bryan M; Dawson Gary; McGovern Dermot P B; Negoro Kenichi; Carey Alisoun H; Cardon Lon R; Mackay Ian; Jewell Derek P; Lench Nicholas J
The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants.
Human molecular genetics 2003;12(20):2569-75.
2003: Duncan Emma L; Cardon Lon R; Sinsheimer Janet S; Wass John A H; Brown Matthew A
Site and gender specificity of inheritance of bone mineral density.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003;18(8):1531-8.
2003: Mitsos Loukia-Maria; Cardon Lon R; Ryan Lynn; LaCourse Ronald; North Robert J; Gros Philippe
Susceptibility to tuberculosis: a locus on mouse chromosome 19 (Trl-4) regulates Mycobacterium tuberculosis replication in the lungs.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(11):6610-5.
2003: Negoro K; McGovern D P B; Kinouchi Y; Takahashi S; Lench N J; Shimosegawa T; Carey A; Cardon L R; Jewell D P; van Heel D A
Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease.
Gut 2003;52(4):541-6.
2003: Cardon Lon R; Abecasis Gonçalo R
Using haplotype blocks to map human complex trait loci.
Trends in genetics : TIG 2003;19(3):135-40.
2003: Marlow Angela J; Fisher Simon E; Francks Clyde; MacPhie I Laurence; Cherny Stacey S; Richardson Alex J; Talcott Joel B; Stein John F; Monaco Anthony P; Cardon Lon R
Use of multivariate linkage analysis for dissection of a complex cognitive trait.
American journal of human genetics 2003;72(3):561-70.
2003: Cardon Lon R; Palmer Lyle J
Population stratification and spurious allelic association.
Lancet 2003;361(9357):598-604.
2003: Ke Xiayi; Cardon Lon R
Efficient selective screening of haplotype tag SNPs.
Bioinformatics (Oxford, England) 2003;19(2):287-8.
2002: Wiltshire Steven; Cardon Lon R; McCarthy Mark I
Evaluating the results of genomewide linkage scans of complex traits by locus counting.
American journal of human genetics 2002;71(5):1175-82.
2002: Kirk Katherine M; Cardon Lon R
The impact of genotyping error on haplotype reconstruction and frequency estimation.
European journal of human genetics : EJHG 2002;10(10):616-22.
2002: van Heel David A; McGovern Dermot P B; Cardon Lon R; Dechairo Bryan M; Lench Nicholas J; Carey Alisoun H; Jewell Derek P
Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: implications for complex disease genetics.
American journal of medical genetics 2002;111(3):253-9.
2002: Dawson Elisabeth; Abecasis Gonçalo R; Bumpstead Suzannah; Chen Yuan; Hunt Sarah; Beare David M; Pabial Jagjit; Dibling Thomas; Tinsley Emma; Kirby Susan; Carter David; Papaspyridonos Marianna; Livingstone Simon; Ganske Rocky; Lõhmussaar Elin; Zernant Jana; Tõnisson Neeme; Remm Maido; Mägi Reedik; Puurand Tarmo; Vilo Jaak; Kurg Ants; Rice Kate; Deloukas Panos; Mott Richard; Metspalu Andres; Bentley David R; Cardon Lon R; Dunham Ian
A first-generation linkage disequilibrium map of human chromosome 22.
Nature 2002;418(6897):544-8.
2002: Zondervan Krina T; Cardon Lon R; Kennedy Stephen H
What makes a good case-control study? Design issues for complex traits such as endometriosis.
Human reproduction (Oxford, England) 2002;17(6):1415-23.
2002: van Heel David A; Udalova Irina A; De Silva Arjuna P; McGovern Dermot P; Kinouchi Yoshitaka; Hull Jeremy; Lench Nicholas J; Cardon Lon R; Carey Alisoun H; Jewell Derek P; Kwiatkowski Dominic
Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF(-kappa)B transcription factors.
Human molecular genetics 2002;11(11):1281-9.
2002: Willcutt Erik G; Pennington Bruce F; Smith Shelley D; Cardon Lon R; Gayán Javier; Knopik Valerie S; Olson Richard K; DeFries John C
Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder.
American journal of medical genetics 2002;114(3):260-8.
2002: Pettipher Roy; Cardon Lon R
The application of genetics to the discovery of better medicines.
Pharmacogenomics 2002;3(2):257-63.
2002: Wiltshire Steven; Frayling Timothy M; Hattersley Andrew T; Hitman Graham A; Walker Mark; Levy Jonathan C; O'Rahilly Stephen; Groves Christopher J; Menzel Stephan; Cardon Lon R; McCarthy Mark I
Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes.
American journal of human genetics 2002;70(2):543-6.
2002: Fisher Simon E; Francks Clyde; Marlow Angela J; MacPhie I Laurence; Newbury Dianne F; Cardon Lon R; Ishikawa-Brush Yumiko; Richardson Alex J; Talcott Joel B; Gayán Javier; Olson Richard K; Pennington Bruce F; Smith Shelley D; DeFries John C; Stein John F; Monaco Anthony P
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Nature genetics 2002;30(1):86-91.
2002: Abecasis Gonçalo R; Cherny Stacey S; Cookson William O; Cardon Lon R
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.
Nature genetics 2002;30(1):97-101.
2001: Davis C J; Gayán J; Knopik V S; Smith S D; Cardon L R; Pennington B F; Olson R K; DeFries J C
Etiology of reading difficulties and rapid naming: the Colorado Twin Study of Reading Disability.
Behavior genetics 2001;31(6):625-35.
2001: Fortin A; Cardon L R; Tam M; Skamene E; Stevenson M M; Gros P
Identification of a new malaria susceptibility locus (Char4) in recombinant congenic strains of mice.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(19):10793-8.
2001: Wiltshire S; Hattersley A T; Hitman G A; Walker M; Levy J C; Sampson M; O'Rahilly S; Frayling T M; Bell J I; Lathrop G M; Bennett A; Dhillon R; Fletcher C; Groves C J; Jones E; Prestwich P; Simecek N; Rao P V; Wishart M; Bottazzo G F; Foxon R; Howell S; Smedley D; Cardon L R; Menzel S; McCarthy M I
A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q.
American journal of human genetics 2001;69(3):553-69.
2001: Abecasis G R; Cherny S S; Cookson W O; Cardon L R
GRR: graphical representation of relationship errors.
Bioinformatics (Oxford, England) 2001;17(8):742-3.
2001: Hamersma J; Cardon L R; Bradbury L; Brophy S; van der Horst-Bruinsma I; Calin A; Brown M A
Is disease severity in ankylosing spondylitis genetically determined?
Arthritis and rheumatism 2001;44(6):1396-400.
2001: Abecasis G R; Cookson W O; Cardon L R
The power to detect linkage disequilibrium with quantitative traits in selected samples.
American journal of human genetics 2001;68(6):1463-74.
2001: Marlow A J; Fisher S E; Richardson A J; Francks C; Talcott J B; Monaco A P; Stein J F; Cardon L R
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK.
Behavior genetics 2001;31(2):219-30.
2001: Abecasis G R; Cherny S S; Cardon L R
The impact of genotyping error on family-based analysis of quantitative traits.
European journal of human genetics : EJHG 2001;9(2):130-4.
2001: Cardon L R; Bell J I
Association study designs for complex diseases.
Nature reviews. Genetics 2001;2(2):91-9.
2001: Abecasis G R; Noguchi E; Heinzmann A; Traherne J A; Bhattacharyya S; Leaves N I; Anderson G G; Zhang Y; Lench N J; Carey A; Cardon L R; Moffatt M F; Cookson W O
Extent and distribution of linkage disequilibrium in three genomic regions.
American journal of human genetics 2001;68(1):191-197.
2001: Abecasis G R; Cardon L R; Cookson W O; Sham P C; Cherny S S
Association analysis in a variance components framework.
Genetic epidemiology 2001;21 Suppl 1():S341-6.
2001: Cherny S S; Abecasis G R; Cookson W O; Sham P C; Cardon L R
The effect of genotype and pedigree error on linkage analysis: analysis of three asthma genome scans.
Genetic epidemiology 2001;21 Suppl 1():S117-22.
2000: Mitsos L M; Cardon L R; Fortin A; Ryan L; LaCourse R; North R J; Gros P
Genetic control of susceptibility to infection with Mycobacterium tuberculosis in mice.
Genes and immunity 2000;1(8):467-77.
2000: Cardon L R
A sib-pair regression model of linkage disequilibrium for quantitative traits.
Human heredity 2000;50(6):350-8.
2000: Abecasis G R; Cookson W O; Cardon L R
Pedigree tests of transmission disequilibrium.
European journal of human genetics : EJHG 2000;8(7):545-51.
2000: Cardon L R; Garner C; Bennett S T; Mackay I J; Edwards R M; Cornish J; Hegde M; Murray M A; Reid I R; Cundy T
Evidence for a major gene for bone mineral density in idiopathic osteoporotic families.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2000;15(6):1132-7.
2000: Cardon L R; Abecasis G R
Some properties of a variance components model for fine-mapping quantitative trait loci.
Behavior genetics 2000;30(3):235-43.
2000: Chavanas S; Garner C; Bodemer C; Ali M; Teillac D H; Wilkinson J; Bonafé J L; Paradisi M; Kelsell D P; Ansai S i; Mitsuhashi Y; Larrègue M; Leigh I M; Harper J I; Taïeb A; Prost Y d; Cardon L R; Hovnanian A
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.
American journal of human genetics 2000;66(3):914-21.
2000: Abecasis G R; Cardon L R; Cookson W O
A general test of association for quantitative traits in nuclear families.
American journal of human genetics 2000;66(1):279-92.
1999: Gayán J; Smith S D; Cherny S S; Cardon L R; Fulker D W; Brower A M; Olson R K; Pennington B F; DeFries J C
Quantitative-trait locus for specific language and reading deficits on chromosome 6p.
American journal of human genetics 1999;64(1):157-64.

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