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ANDREW COLLINS

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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Collins A
Approaches to the identification of susceptibility genes.
Jones Amy V; Chase Andrew; Silver Richard T; Oscier David; Zoi Katerina; Wang Y Lynn; Cario Holger; Pahl Heike L; Collins Andrew; Reiter Andreas; Grand Francis; Cross Nicholas C P
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms.
Gilbert Rodney D; Turner Claire L S; Gibson Jane; Bass Paul S; Haq Mushfequr R; Cross Esta; Bunyan David J; Collins Andrew R; Tapper William J; Needell Juliet C; Dell Beverley; Morton Newton E; Temple I Karen; Robinson David O
Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis.

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All Publications

2009: Collins A
Approaches to the identification of susceptibility genes.
Parasite immunology 2009;31(5):225-33.
2009: Jones Amy V; Chase Andrew; Silver Richard T; Oscier David; Zoi Katerina; Wang Y Lynn; Cario Holger; Pahl Heike L; Collins Andrew; Reiter Andreas; Grand Francis; Cross Nicholas C P
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms.
Nature genetics 2009;41(4):446-9.
2009: Gilbert Rodney D; Turner Claire L S; Gibson Jane; Bass Paul S; Haq Mushfequr R; Cross Esta; Bunyan David J; Collins Andrew R; Tapper William J; Needell Juliet C; Dell Beverley; Morton Newton E; Temple I Karen; Robinson David O
Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis.
Kidney international 2009;75(4):415-9.
2009: Sabatti Chiara; Service Susan K; Hartikainen Anna-Liisa; Pouta Anneli; Ripatti Samuli; Brodsky Jae; Jones Chris G; Zaitlen Noah A; Varilo Teppo; Kaakinen Marika; Sovio Ulla; Ruokonen Aimo; Laitinen Jaana; Jakkula Eveliina; Coin Lachlan; Hoggart Clive; Collins Andrew; Turunen Hannu; Gabriel Stacey; Elliot Paul; McCarthy Mark I; Daly Mark J; Järvelin Marjo-Riitta; Freimer Nelson B; Peltonen Leena
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Nature genetics 2009;41(1):35-46.
2009: Collins Andrew
Allelic association: linkage disequilibrium structure and gene mapping.
Molecular biotechnology 2009;41(1):83-9.
2008: Jakkula Eveliina; Rehnström Karola; Varilo Teppo; Pietiläinen Olli P H; Paunio Tiina; Pedersen Nancy L; deFaire Ulf; Järvelin Marjo-Riitta; Saharinen Juha; Freimer Nelson; Ripatti Samuli; Purcell Shaun; Collins Andrew; Daly Mark J; Palotie Aarno; Peltonen Leena
The genome-wide patterns of variation expose significant substructure in a founder population.
American journal of human genetics 2008;83(6):787-94.
2008: Ennis Sarah; Jomary Catherine; Mullins Robert; Cree Angela; Chen Xiaoli; Macleod Alex; Jones Stephen; Collins Andrew; Stone Edwin; Lotery Andrew
Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study.
Lancet 2008;372(9652):1828-34.
2008: Gibson Jane; Collins Andrew; Morton Newton
Individual disease risk and multimetric analysis of Crohn disease.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(41):15843-7.
2008: Gibson Jane; Tapper William; Cox David; Zhang Weihua; Pfeufer Arne; Gieger Christian; Wichmann H-Erich; Kääb Stefan; Collins Andrew R; Meitinger Thomas; Morton Newton
A multimetric approach to analysis of genome-wide association by single markers and composite likelihood.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(7):2592-7.
2008: Tapper William; Hammond Victoria; Gerty Sue; Ennis Sarah; Simmonds Peter; Collins Andrew; Eccles Diana
The influence of genetic variation in 30 selected genes on the clinical characteristics of early onset breast cancer.
Breast cancer research : BCR 2008;10(6):R108.
2008: Khatkar Mehar S; Nicholas Frank W; Collins Andrew R; Zenger Kyall R; Cavanagh Julie A L; Barris Wes; Schnabel Robert D; Taylor Jeremy F; Raadsma Herman W
Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panel.
BMC genomics 2008;9():187.
2008: Tapper William; Gibson Jane; Morton Newton E; Collins Andrew
A comparison of methods to detect recombination hotspots.
Human heredity 2008;66(3):157-69.
2008: Collins Andrew; Lau Winston
CHROMSCAN: genome-wide association using a linkage disequilibrium map.
Journal of human genetics 2008;53(2):121-6.
2007: Hall Heather E; Chan E Ricky; Collins Andrew; Judis LuAnn; Shirley Sofia; Surti Urvashi; Hoffner Lori; Cockwell Annette E; Jacobs Patricia A; Hassold Terry J
The origin of trisomy 13.
American journal of medical genetics. Part A 2007;143A(19):2242-8.
2007: Bugge Merete; Collins Andrew; Hertz Jens Michael; Eiberg Hans; Lundsteen Claes; Brandt Carsten A; Bak Mads; Hansen Claus; Delozier Celia D; Lespinasse James; Tranebjaerg Lisbeth; Hahnemann Johanne M D; Rasmussen Kirsten; Bruun-Petersen Gert; Duprez Laurence; Tommerup Niels; Petersen Michael B
Non-disjunction of chromosome 13.
Human molecular genetics 2007;16(16):2004-10.
2007: Ennis Sarah; Goverdhan Srini; Cree Angela; Hoh Josephine; Collins Andrew; Lotery Andrew
Fine-scale linkage disequilibrium mapping of age-related macular degeneration in the complement factor H gene region.
The British journal of ophthalmology 2007;91(7):966-70.
2007: Liao Webber; Collins Andrew; Hobbs Matthew; Khatkar Mehar S; Luo Junhong; Nicholas Frank W
A comparative location database (CompLDB): map integration within and between species.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(5):287-99.
2007: Maniatis Nikolas; Collins Andrew; Morton Newton E
Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.
Genetic epidemiology 2007;31(3):179-88.
2007: Abdollahi Mohammad R; Lewis Rohan M; Gaunt Tom R; Cumming Debbie V E; Rodriguez Santiago; Rose-Zerilli Matthew; Collins Andrew R; Syddall Holly E; Howell William M; Cooper Cyrus; Godfrey Keith M; Cameron Iain T; Day Ian N M
Quantitated transcript haplotypes (QTH) of AGTR1, reduced abundance of mRNA haplotypes containing 1166C (rs5186:A>C), and relevance to metabolic syndrome traits.
Human mutation 2007;28(4):365-73.
2007: Lau Winston; Kuo Tai-Yue; Tapper William; Cox Simon; Collins Andrew
Exploiting large scale computing to construct high resolution linkage disequilibrium maps of the human genome.
Bioinformatics (Oxford, England) 2007;23(4):517-9.
2007: Morton Newton; Maniatis Nikolas; Zhang Weihua; Ennis Sarah; Collins Andrew
Genome scanning by composite likelihood.
American journal of human genetics 2007;80(1):19-28.
2007: Tapper William; Collins Andrew; Morton Newton E
Mapping a gene for rheumatoid arthritis on chromosome 18q21.
BMC proceedings 2007;1 Suppl 1():S18.
2007: Kuo Tai-Yue; Lau Winston; Collins Andrew R
LDMAP: the construction of high-resolution linkage disequilibrium maps of the human genome.
Methods in molecular biology (Clifton, N.J.) 2007;376():47-57.
2007: Collins Andrew R
Linkage disequilibrium and association mapping: an introduction.
Methods in molecular biology (Clifton, N.J.) 2007;376():1-15.
2007: Pereira Lutécia H Mateus; Pineda Marbin A; Rowe William H; Fonseca Libia R; Greene Mark H; Offit Kenneth; Ellis Nathan A; Zhang Jinghui; Collins Andrew; Struewing Jeffery P
The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies.
BMC genetics 2007;8():68.
2006: Zhang W; Maniatis N; Rodriguez S; Miller G J; Day I N M; Gaunt T R; Collins A; Morton N E
Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH region.
Annals of human genetics 2006;70(Pt 6):848-56.
2006: Khatkar Mehar S; Collins Andrew; Cavanagh Julie A L; Hawken Rachel J; Hobbs Matthew; Zenger Kyall R; Barris Wes; McClintock Alexander E; Thomson Peter C; Nicholas Frank W; Raadsma Herman W
A first-generation metric linkage disequilibrium map of bovine chromosome 6.
Genetics 2006;174(1):79-85.
2006: Service Susan; DeYoung Joseph; Karayiorgou Maria; Roos J Louw; Pretorious Herman; Bedoya Gabriel; Ospina Jorge; Ruiz-Linares Andres; Macedo António; Palha Joana Almeida; Heutink Peter; Aulchenko Yurii; Oostra Ben; van Duijn Cornelia; Jarvelin Marjo-Riitta; Varilo Teppo; Peddle Lynette; Rahman Proton; Piras Giovanna; Monne Maria; Murray Sarah; Galver Luana; Peltonen Leena; Sabatti Chiara; Collins Andrew; Freimer Nelson
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
Nature genetics 2006;38(5):556-60.
2006: Gibson Jane; Morton Newton E; Collins Andrew
Extended tracts of homozygosity in outbred human populations.
Human molecular genetics 2006;15(5):789-95.
2006: Self James Edward; Ennis Sarah; Collins Andrew; Shawkat Fatima; Harris Christopher Mark; Mackey David Anthony; Hodgkins Peter Robert; Temple Isabelle Karen; Chen Xiaoli; Lotery Andrew John
Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.
Molecular vision 2006;12():1211-6.
2006: Chen Lina; Velasco Mondragón H Eduardo; Lazcano-Ponce Eduardo; Collins Andrew; Shugart Yin Yao
Effect of the peroxisome proliferators-activated receptor (PPAR) gamma 3 gene on BMI in 1,210 school students from Morelos, Mexico.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2006;():467-77.
2005: Tapper W; Collins A; Gibson J; Maniatis N; Ennis S; Morton N E
A map of the human genome in linkage disequilibrium units.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(33):11835-9.
2005: Simpson Angela; Maniatis Nikolas; Jury Francine; Cakebread Julie A; Lowe Lesley A; Holgate Stephen T; Woodcock Ashley; Ollier William E R; Collins Andrew; Custovic Adnan; Holloway John W; John Sally L
Polymorphisms in a disintegrin and metalloprotease 33 (ADAM33) predict impaired early-life lung function.
American journal of respiratory and critical care medicine 2005;172(1):55-60.
2005: De La Vega Francisco M; Isaac Hadar; Collins Andrew; Scafe Charles R; Halldórsson Bjarni V; Su Xiaoping; Lippert Ross A; Wang Yu; Laig-Webster Marion; Koehler Ryan T; Ziegle Janet S; Wogan Lewis T; Stevens Junko F; Leinen Kyle M; Olson Sheri J; Guegler Karl J; You Xiaoqing; Xu Lily H; Hemken Heinz G; Kalush Francis; Itakura Mitsuo; Zheng Yi; de Thé Guy; O'Brien Stephen J; Clark Andrew G; Istrail Sorin; Hunkapiller Michael W; Spier Eugene G; Gilbert Dennis A
The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern.
Genome research 2005;15(4):454-62.
2005: Gibson Jane; Tapper William; Zhang Weihua; Morton Newton; Collins Andrew
Cosmopolitan linkage disequilibrium maps.
Human genomics 2005;2(1):20-7.
2005: Scapoli C; Trombelli L; Mamolini E; Collins A
Linkage disequilibrium analysis of case-control data: an application to generalized aggressive periodontitis.
Genes and immunity 2005;6(1):44-52.
2005: Jia Wei-Hua; Collins Andrew; Zeng Yi-Xin; Feng Bing-Jian; Yu Xing-Juan; Huang Li-Xi; Feng Qi-Sheng; Huang Ping; Yao Ming-Hong; Shugart Yin Yao
Complex segregation analysis of nasopharyngeal carcinoma in Guangdong, China: evidence for a multifactorial mode of inheritance (complex segregation analysis of NPC in China).
European journal of human genetics : EJHG 2005;13(2):248-52.
2005: Maniatis N; Morton N E; Gibson J; Xu C-F; Hosking L K; Collins A
The optimal measure of linkage disequilibrium reduces error in association mapping of affection status.
Human molecular genetics 2005;14(1):145-53.
2004: Zhang Weihua; Collins Andrew; Gibson Jane; Tapper William J; Hunt Sarah; Deloukas Panos; Bentley David R; Morton Newton E
Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(52):18075-80.
2004: Simpson Claire L; Hansen Valerie K; Sham Pak C; Collins Andrew; Powell John F; Al-Chalabi Ammar
MaGIC: a program to generate targeted marker sets for genome-wide association studies.
BioTechniques 2004;37(6):996-9.
2004: Zhang Weihua; Collins Andrew; Morton Newton E
Does haplotype diversity predict power for association mapping of disease susceptibility?
Human genetics 2004;115(2):157-64.
2004: Maniatis Nikolas; Collins Andrew; Gibson Jane; Zhang Weihua; Tapper William; Morton Newton E
Positional cloning by linkage disequilibrium.
American journal of human genetics 2004;74(5):846-55.
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: Collins Andrew; Lau Winston; De La Vega Francisco M
Mapping genes for common diseases: the case for genetic (LD) maps.
Human heredity 2004;58(1):2-9.
2003: Tapper W J; Maniatis N; Morton N E; Collins A
A metric linkage disequilibrium map of a human chromosome.
Annals of human genetics 2003;67(Pt 6):487-94.
2003: Ye Shu; Dunleavey Louise; Bannister Wendy; Day Lorna B; Tapper William; Collins Andrew R; Day Ian N M; Simpson Iain;
Independent effects of the -219 G>T and epsilon 2/ epsilon 3/ epsilon 4 polymorphisms in the apolipoprotein E gene on coronary artery disease: the Southampton Atherosclerosis Study.
European journal of human genetics : EJHG 2003;11(6):437-43.
2003: Ke X; Collins A
CpG islands in human X-inactivation.
Annals of human genetics 2003;67(Pt 3):242-9.
2003: Morgan Angharad R; Zhang Baiping; Tapper William; Collins Andrew; Ye Shu
Haplotypic analysis of the MMP-9 gene in relation to coronary artery disease.
Journal of molecular medicine (Berlin, Germany) 2003;81(5):321-6.
2003: Lonjou Christine; Zhang Weihua; Collins Andrew; Tapper William J; Elahi Eiram; Maniatis Nikolas; Morton Newton E
Linkage disequilibrium in human populations.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(10):6069-74.
2002: Shugart Yin Y; Feng Bing-Jian; Collins Andrew
The power and statistical behaviour of allele-sharing statistics when applied to models with two disease loci.
Journal of genetics 2002;81(3):99-103.
2002: Ke Xiayi; Collins Andrew; Ye Shu
PCR designer for restriction analysis of various types of sequence mutation.
Bioinformatics (Oxford, England) 2002;18(12):1688-9.
2002: Zhang Weilhua; Collins Andrew; Maniatis Nikolas; Tapper William; Morton Newton E
Properties of linkage disequilibrium (LD) maps.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(26):17004-7.
2002: Ke Xiayi; Thomas N Simon; Robinson David O; Collins Andrew
A novel approach for identifying candidate imprinted genes through sequence analysis of imprinted and control genes.
Human genetics 2002;111(6):511-20.
2002: Ke Xiayi; Thomas N Simon; Robinson David O; Collins Andrew
The distinguishing sequence characteristics of mouse imprinted genes.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(11):639-45.
2002: Fredell Louise; Iselius Lennart; Collins Andy; Hansson Einar; Holmner Staffan; Lundquist Lars; Läckgren Göran; Pedersen Jörgen; Stenberg Arne; Westbacke Gunnar; Nordenskjöld Agneta
Complex segregation analysis of hypospadias.
Human genetics 2002;111(3):231-4.
2002: Peacock C S; Sanjeevi C B; Shaw M-A; Collins A; Campbell R D; March R; Silveira F; Costa J; Coste C H; Nascimento M D; Siddiqui R; Shaw J J; Blackwell J M
Genetic analysis of multicase families of visceral leishmaniasis in northeastern Brazil: no major role for class II or class III regions of HLA.
Genes and immunity 2002;3(6):350-8.
2002: Morton Newton E; Collins Andrew
Toward positional cloning with SNPs.
Current opinion in molecular therapeutics 2002;4(3):259-64.
2002: Howell W M; Bateman A C; Turner S J; Collins A; Theaker J M
Influence of vascular endothelial growth factor single nucleotide polymorphisms on tumour development in cutaneous malignant melanoma.
Genes and immunity 2002;3(4):229-32.
2002: Zhang W; Collins A; Abecasis G R; Cardon L R; Morton N E
Mapping quantitative effects of oligogenes by allelic association.
Annals of human genetics 2002;66(Pt 3):211-21.
2002: Maniatis N; Collins A; Xu C F; McCarthy L C; Hewett D R; Tapper W; Ennis S; Ke X; Morton N E
The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(4):2228-33.
2002: Howell W M; Turner S J; Collins A; Bateman A C; Theaker J M
Influence of TNFalpha and LTalpha single nucleotide polymorphisms on susceptibility to and prognosis in cutaneous malignant melanoma in the British population.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 2002;29(1):17-23.
2002: Zhang W; Collins A; Lonjou C; Morton N E;
A linkage tournament: affection status, parametric analysis, multivariate traits, and enhancements to variance components and relative pairs.
Annals of human genetics 2002;66(Pt 1):87-98.
2002: Tapper W J; Ke X; Morton N E; Collins A
Recombination, interference and sequence: comparison of chromosomes 21 and 22.
Annals of human genetics 2002;66(Pt 1):75-86.
2001: Ennis S; Maniatis N; Collins A
Allelic association and disease mapping.
Briefings in bioinformatics 2001;2(4):375-87.
2001: Ennis S; Collins A; Tapper W; Murray A; MacPherson J N; Morton N E
Allelic association discriminates draft orders.
Annals of human genetics 2001;65(Pt 5):503-4.
2001: Ke X; Collins A; Ye S
PIRA PCR designer for restriction analysis of single nucleotide polymorphisms.
Bioinformatics (Oxford, England) 2001;17(9):838-9.
2001: Ye S; Dhillon S; Ke X; Collins A R; Day I N
An efficient procedure for genotyping single nucleotide polymorphisms.
Nucleic acids research 2001;29(17):E88-8.
2001: Ke X; Tapper W; Collins A
LDB2000: sequence-based integrated maps of the human genome.
Bioinformatics (Oxford, England) 2001;17(7):581-6.
2001: Tapper W J; Morton N E; Dunham I; Ke X; Collins A
A sequence-based integrated map of chromosome 22.
Genome research 2001;11(7):1290-5.
2001: Shaw M A; Donaldson I J; Collins A; Peacock C S; Lins-Lainson Z; Shaw J J; Ramos F; Silveira F; Blackwell J M
Association and linkage of leprosy phenotypes with HLA class II and tumour necrosis factor genes.
Genes and immunity 2001;2(4):196-204.
2001: Morton N E; Zhang W; Taillon-Miller P; Ennis S; Kwok P Y; Collins A
The optimal measure of allelic association.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(9):5217-21.
2001: Collins A; Ennis S; Taillon-Miller P; Kwok P Y; Morton N E
Allelic association with SNPs: metrics, populations, and the linkage disequilibrium map.
Human mutation 2001;17(4):255-62.
2001: Peacock C S; Collins A; Shaw M A; Silveira F; Costa J; Coste C H; Nascimento M D; Siddiqui R; Shaw J J; Blackwell J M
Genetic epidemiology of visceral leishmaniasis in northeastern Brazil.
Genetic epidemiology 2001;20(3):383-96.
2001: Malmer B; Iselius L; Holmberg E; Collins A; Henriksson R; Grönberg H
Genetic epidemiology of glioma.
British journal of cancer 2001;84(3):429-34.
2001: Thomas N S; Ennis S; Sharp A J; Durkie M; Hassold T J; Collins A R; Jacobs P A
Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors.
Human molecular genetics 2001;10(3):243-50.
2001: Zhang W; Tapper W; Collins A; Jacobs K B; Elston R C; Morton N E
A tournament of linkage tests in complex inheritance.
Human heredity 2001;52(3):140-8.
2001: Zhang W; Collins A; Morton N E
Combination of linkage evidence in complex inheritance.
Human heredity 2001;52(3):132-5.
2000: Ennis S; Collins A; Murray A; Macpherson J N; Morton N E
Allelic association in the FRAX region.
Annals of human genetics 2000;64(Pt 6):513-8.
2000: Forabosco P; Collins A; Latiano A; Annese V; Clementi M; Andriulli A; Fortina P; Devoto M; Morton N E
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis. On behalf of the GISC.
European journal of human genetics : EJHG 2000;8(11):846-52.
2000: Thomas N S; Collins A R; Hassold T J; Jacobs P A
A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin.
European journal of human genetics : EJHG 2000;8(10):805-8.
2000: Shugart Y Y; Collins A
Combined segregation and linkage analysis of 59 Hodgkin's disease families indicates the role of HLA determinants.
European journal of human genetics : EJHG 2000;8(6):460-3.
2000: McMullan T F; Collins A R; Tyers A G; Robinson D O
A novel X-linked dominant condition: X-linked congenital isolated ptosis.
American journal of human genetics 2000;66(4):1455-60.
2000: Collins A
Mapping in the sequencing era.
Human heredity 2000;50(1):76-84.
2000: Collins A
Linkage disequilibrium mapping using single nucleotide polymorphisms--which population?
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2000;():651-62.
1999: Lonjou C; Collins A; Ennis S; Tapper W; Morton N E
Meta-analysis and retrospective collaboration: two methods to map oligogenes for atopy and asthma.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1999;29 Suppl 4():57-9.
1999: Collins A
Mapping disease genes using the Malecot model for allelic association and the beta model for linkage.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1999;29 Suppl 4():53-6.
1999: Collins A; Lonjou C; Morton N E
Genetic epidemiology of single-nucleotide polymorphisms.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(26):15173-7.
1999: Gomes I; Collins A; Lonjou C; Thomas N S; Wilkinson J; Watson M; Morton N
Hardy-Weinberg quality control.
Annals of human genetics 1999;63(Pt 6):535-8.
1999: Lonjou C; Collins A; Morton N E
Allelic association between marker loci.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(4):1621-6.
1999: Scapoli C; Collins A; Martinelli M; Pezzetti F; Scapoli L; Tognon M
Combined segregation and linkage analysis of nonsyndromic orofacial cleft in two candidate regions.
Annals of human genetics 1999;63(Pt 1):17-25.
1999: Shugart Y Y; Wehman P; Collins A
An evaluation of affected-sib-pair methods and transmission/disequilibrium tests for detecting genes underlying a complex trait.
Genetic epidemiology 1999;17 Suppl 1():S727-30.
1999: Fann C S; Shugart Y Y; Lachman H; Collins A; Chang C J
The impact of redefining affection status for alcoholism on affected-sib-pair analysis.
Genetic epidemiology 1999;17 Suppl 1():S151-6.
1998: Lonjou C; Collins A; Beckmann J; Allamand V; Morton N
Limb girdle muscular dystrophy type 2A (CAPN3): mapping using allelic association.
Human heredity 1998;48(6):333-7.
1998: Wilkinson J; Grimley S; Collins A; Thomas N S; Holgate S T; Morton N
Linkage of asthma to markers on chromosome 12 in a sample of 240 families using quantitative phenotype scores.
Genomics 1998;53(3):251-9.
1998: Morton N E; Collins A
Tests and estimates of allelic association in complex inheritance.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(19):11389-93.
1998: Lonjou C; Collins A; Ajioka R S; Jorde L B; Kushner J P; Morton N E
Allelic association under map error and recombinational heterogeneity: a tale of two sites.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(19):11366-70.
1998: Bugge M; Collins A; Petersen M B; Fisher J; Brandt C; Hertz J M; Tranebjaerg L; de Lozier-Blanchet C; Nicolaides P; Brøndum-Nielsen K; Morton N; Mikkelsen M
Non-disjunction of chromosome 18.
Human molecular genetics 1998;7(4):661-9.
1998: Collins A; Morton N E
Mapping a disease locus by allelic association.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(4):1741-5.
1997: Blackwell J M; Black G F; Peacock C S; Miller E N; Sibthorpe D; Gnananandha D; Shaw J J; Silveira F; Lins-Lainson Z; Ramos F; Collins A; Shaw M A
Immunogenetics of leishmanial and mycobacterial infections: the Belem Family Study.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1997;352(1359):1331-45.
1997: Scapoli C; Collins A; Benatti P; Percesepe A; Roncucci L; Ponz de Leon M
A two-locus model for hereditary non-polyposis colorectal cancer in Modena, Italy.
Annals of human genetics 1997;61(Pt 2):109-19.
1997: Morton N E; Collins A
The future of gene mapping.
Genetic analysis : biomolecular engineering 1997;14(1):25-7.
1997: Shaw M A; Collins A; Peacock C S; Miller E N; Black G F; Sibthorpe D; Lins-Lainson Z; Shaw J J; Ramos F; Silveira F; Blackwell J M
Evidence that genetic susceptibility to Mycobacterium tuberculosis in a Brazilian population is under oligogenic control: linkage study of the candidate genes NRAMP1 and TNFA.
Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease 1997;78(1):35-45.
1996: Collins A; Frezal J; Teague J; Morton N E
A metric map of humans: 23,500 loci in 850 bands.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(25):14771-5.
1996: Teague J W; Collins A; Morton N E
Studies on locus content mapping.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(21):11814-8.
1996: Collins A; Teague J; Keats B J; Morton N E
Linkage map integration.
Genomics 1996;36(1):157-62.
1996: Collins A; MacLean C J; Morton N E
Trials of the beta model for complex inheritance.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(17):9177-81.
1996: Silverman G A; Overhauser J; Gerken S; Aburomia R; O'Connell P; Krauter K S; Detera-Wadleigh S D; Yoshikawa T; Collins A R; Geurts van Kessel A
Report of the Fourth International Workshop on Human Chromosome 18 Mapping. Boston, Massachusetts, October 7-9, 1996.
Cytogenetics and cell genetics 1996;75(2-3):111-31.
1995: Collins A; Morton N E
Nonparametric tests for linkage with dependent sib pairs.
Human heredity 1995;45(6):311-8.
1995: Shaw M A; Davies C R; Llanos-Cuentas E A; Collins A
Human genetic susceptibility and infection with Leishmania peruviana.
American journal of human genetics 1995;57(5):1159-68.
1995: Cox S; Bryant S P; Collins A; Weissenbach J; Donis-Keller H; Koeleman B P; Steinkasserer A; Spurr N K
Integrated genetic map of human chromosome 2.
Annals of human genetics 1995;59(Pt 4):413-34.
1995: Watson M; Lawrence S; Collins A; Beasley R; Doull I; Begishvili B; Lampe F; Holgate S T; Morton N E
Exclusion from proximal 11q of a common gene with megaphenic effect on atopy.
Annals of human genetics 1995;59(Pt 4):403-11.
1995: Collins A; Forabosco P; Lawrence S; Morton N E
An integrated map of chromosome 9.
Annals of human genetics 1995;59(Pt 4):393-402.
1995: Morton N E; Collins A E
Statistical and genetic aspects of quality control for DNA identification.
Electrophoresis 1995;16(9):1670-7.
1995: Forabosco P; Collins A; Morton N E
Integration of gene maps: updating chromosome 1.
Annals of human genetics 1995;59(Pt 3):291-305.
1995: Morris A; Morton N E; Collins A; Lawrence S; Macpherson J N
Evolutionary dynamics of the FMR1 locus.
Annals of human genetics 1995;59(Pt 3):283-9.
1995: Morris A; Morton N E; Collins A; Macpherson J; Nelson D; Sherman S
An n-allele model for progressive amplification in the FMR1 locus.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(11):4833-7.
1995: Clementi M; Tenconi R; Collins A; Calzolari E; Milan M
Complex segregation analysis in a sample of consecutive newborns with cleft lip with or without cleft palate in Italy.
Human heredity 1995;45(3):157-64.
1995: Houlston R S; Collins A; Kee F; Collins B J; Shields D C; Morton N E
Segregation analysis of colorectal cancer in Northern Ireland.
Human heredity 1995;45(1):41-8.
1994: Eccles D; Marlow A; Royle G; Collins A; Morton N E
Genetic epidemiology of early onset breast cancer.
Journal of medical genetics 1994;31(12):944-9.
1994: Shields D C; Ratanachaiyavong S; McGregor A M; Collins A; Morton N E
Combined segregation and linkage analysis of Graves disease with a thyroid autoantibody diathesis.
American journal of human genetics 1994;55(3):540-54.
1994: Wang L H; Collins A; Lawrence S; Keats B J; Morton N E
Integration of gene maps: chromosome X.
Genomics 1994;22(3):590-604.
1994: Scapoli C; Ponz De Leon M; Sassatelli R; Benatti P; Roncucci L; Collins A; Morton N E; Barrai I
Genetic epidemiology of hereditary non-polyposis colorectal cancer syndromes in Modena, Italy: results of a complex segregation analysis.
Annals of human genetics 1994;58(Pt 3):275-95.
1994: Collins A; Morton N E
Likelihood ratios for DNA identification.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(13):6007-11.
1994: Attwood J; Chiano M; Collins A; Donis-Keller H; Dracopoli N; Fountain J; Falk C; Goudie D; Gusella J; Haines J
CEPH consortium Map of chromosome 9.
Genomics 1994;19(2):203-14.
1994: Sham P C; Morton N E; Muir W J; Walker M; Collins A; Shields D C; St Clair D M; Blackwood D H
Segregation analysis of complex phenotypes: an application to schizophrenia and auditory P300 latency.
Psychiatric genetics 1994;4(1):29-38.
1994: Shields D C; Collins A; Marlow A
Coding of pointers in the segregation analysis program POINTER.
Genetic epidemiology 1994;11(4):385-7.
1993: Lawrence S; Collins A; Keats B J; Hulten M; Morton N E
Integration of gene maps: chromosome 21.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(15):7210-4.
1993: Morton N E; Collins A; Balazs I
Kinship bioassay on hypervariable loci in blacks and Caucasians.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(5):1892-6.
1992: Morton N E; Collins A; Lawrence S; Shields D C
Algorithms for a location database.
Annals of human genetics 1992;56(Pt 3):223-32.
1992: Collins A; Keats B J; Dracopoli N; Shields D C; Morton N E
Integration of gene maps: chromosome 1.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(10):4598-602.
1992: Houlston R S; Collins A; Slack J; Morton N E
Dominant genes for colorectal cancer are not rare.
Annals of human genetics 1992;56(Pt 2):99-103.
1991: Morton N E; Shields D C; Collins A
Genetic epidemiology of complex phenotypes.
Annals of human genetics 1991;55(Pt 4):301-14.
1991: Houlston R S; Collins A; Slack J; Campbell S; Collins W P; Whitehead M I; Morton N E
Genetic epidemiology of ovarian cancer: segregation analysis.
Annals of human genetics 1991;55(Pt 4):291-9.
1991: Shields D C; Collins A; Buetow K H; Morton N E
Error filtration, interference, and the human linkage map.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(15):6501-5.
1991: Collins A; Morton N E
Significance of maximal lods.
Annals of human genetics 1991;55(Pt 1):39-41.
1990: Morton N E; Collins A
Standard maps of chromosome 10.
Annals of human genetics 1990;54(Pt 3):235-51.
1990: Morton N E; Collins A
Counting algorithms for linkage.
Annals of human genetics 1990;54(Pt 2):103-6.

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