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Research Output 1997 2018

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Article
2018

Bone marrow-derived epithelial cells and hair follicle stem cells contribute to development of chronic cutaneous neoplasms

Park, H., Lad, S., Boland, K., Johnson, K., Readio, N., Jin, G., Asfaha, S., Patterson, K. S., Singh, A., Yang, X., Londono, D., Singh, A., Trempus, C., Gordon, D., Wang, T. C. & Morris, R. J., Dec 1 2018, In : Nature communications. 9, 1, 5293.

Research output: Contribution to journalArticle

neoplasms
Hair Follicle
bone marrow
stem cells
hair
5 Citations (Scopus)

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

Abdulkadir, M., Londono, D., Gordon, D., Fernandez, T. V., Brown, L. W., Cheon, K. A., Coffey, B. J., Elzerman, L., Fremer, C., Fründt, O., Garcia-Delgar, B., Gilbert, D. L., Grice, D. E., Hedderly, T., Heyman, I., Hong, H. J., Huyser, C., Ibanez-Gomez, L., Jakubovski, E., Kim, Y. K. & 29 others, Kim, Y. S., Koh, Y. J., Kook, S., Kuperman, S., Leventhal, B., Ludolph, A. G., Madruga-Garrido, M., Maras, A., Mir, P., Morer, A., Müller-Vahl, K., Münchau, A., Murphy, T. L., Plessen, K. J., Roessner, V., Shin, E. Y., Song, D. H., Song, J., Tübing, J., van den Ban, E., Visscher, F., Wanderer, S., Woods, M., Zinner, S. H., King, R. A., Tischfield, J. A., Heiman, G. A., Hoekstra, P. J. & Dietrich, A., Apr 1 2018, In : European Archives of Psychiatry and Clinical Neuroscience. 268, 3, p. 301-316 16 p.

Research output: Contribution to journalArticle

Tic Disorders
Single Nucleotide Polymorphism
Tourette Syndrome
Genome-Wide Association Study
Genes
2017

An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance

Gordon, D., Londono, D., Patel, P., Kim, W., Finch, S. J. & Heiman, G. A., May 1 2017, In : Human Heredity. 81, 4, p. 194-209 16 p.

Research output: Contribution to journalArticle

Genetic Association Studies
Sample Size
Genotype
Phenotype
Analysis of Variance
2015
57 Citations (Scopus)

A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

TSRHC Scoliosis Clinical Group & Japan Scoliosis Clinical Research Group, 2015, In : Nature communications. 6, 6452.

Research output: Contribution to journalArticle

Pediatrics
Scoliosis
loci
Muscle
Transcription Factors
11 Citations (Scopus)

Expression and characterization of three Aurora kinase C splice variants found in human oocytes

Fellmeth, J. E., Gordon, D., Robins, C. E., Scott, R. T., Treff, N. R. & Schindler, K., Mar 10 2015, In : Molecular human reproduction. 21, 8, p. 633-644 12 p.

Research output: Contribution to journalArticle

Aurora Kinase C
Oocytes
Meiosis
Chromosome Segregation
Metaphase
2014
35 Citations (Scopus)

A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups

Londono, D., Kou, I., Johnson, T. A., Sharma, S., Ogura, Y., Tsunoda, T., Takahashi, A., Matsumoto, M., Herring, J. A., Lam, T. P., Wang, X., Tam, E. M. S., Song, Y. Q., Fan, Y. H., Chan, D., Cheah, K. S. E., Qiu, X., Jiang, H., Huang, D., Su, P. & 9 others, Sham, P., Cheung, K. M. C., Luk, K. D. K., Gordon, D., Qiu, Y., Cheng, J., Tang, N., Ikegawa, S. & Wise, C. A., Jan 1 2014, In : Journal of medical genetics. 51, 6, p. 401-406 6 p.

Research output: Contribution to journalArticle

Scoliosis
Ethnic Groups
Meta-Analysis
Genome-Wide Association Study
Genes
6 Citations (Scopus)

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

Musolf, A., Nato, A. Q., Londono, D., Zhou, L., Matise, T. & Gordon, D., Jun 17 2014, In : BMC Proceedings. 8, S81.

Research output: Contribution to journalArticle

Chromosome Mapping
Genes
Phenotype
Disease Progression
Blood Pressure
10 Citations (Scopus)

Novel cystine ester mimics for the treatment of cystinuria-induced urolithiasis in a knockout mouse model

Sahota, A., Parihar, J. S., Capaccione, K. M., Yang, M., Noll, K., Gordon, D., Reimer, D., Yang, I., Buckley, B. T., Polunas, M., Reuhl, K. R., Lewis, M. R., Ward, M. D., Goldfarb, D. S. & Tischfield, J. A., Nov 1 2014, In : Urology. 84, 5, p. 1249.e9-1249.e15

Research output: Contribution to journalArticle

Cystinuria
Urolithiasis
Cystine
Knockout Mice
Esters
2013
26 Citations (Scopus)

A keratin 15 containing stem cell population from the hair follicle contributes to squamous papilloma development in the mouse

Li, S., Park, H., Trempus, C. S., Gordon, D., Liu, Y., Cotsarelis, G. & Morris, R. J., Oct 1 2013, In : Molecular Carcinogenesis. 52, 10, p. 751-759 9 p.

Research output: Contribution to journalArticle

Keratin-15
Hair Follicle
Papilloma
Stem Cells
Population
8 Citations (Scopus)

A novel method for analyzing genetic association with longitudinal phenotypes

Londono, D., Chen, K. M., Musolf, A., Wang, R., Shen, T., Brandon, J., Herring, J. A., Wise, C. A., Zou, H., Jin, M., Yu, L., Finch, S. J., Matise, T. & Gordon, D., May 1 2013, In : Statistical Applications in Genetics and Molecular Biology. 12, 2, p. 241-261 21 p.

Research output: Contribution to journalArticle

Genetic Association
Progression
Phenotype
Tractrix
Genes
110 Citations (Scopus)

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis

Kou, I., Takahashi, Y., Johnson, T. A., Takahashi, A., Guo, L., Dai, J., Qiu, X., Sharma, S., Takimoto, A., Ogura, Y., Jiang, H., Yan, H., Kono, K., Kawakami, N., Uno, K., Ito, M., Minami, S., Yanagida, H., Taneichi, H., Hosono, N. & 21 others, Tsuji, T., Suzuki, T., Sudo, H., Kotani, T., Yonezawa, I., Londono, D., Gordon, D., Herring, J. A., Watanabe, K., Chiba, K., Kamatani, N., Jiang, Q., Hiraki, Y., Kubo, M., Toyama, Y., Tsunoda, T., Wise, C. A., Qiu, Y., Shukunami, C., Matsumoto, M. & Ikegawa, S., Jun 1 2013, In : Nature genetics. 45, 6, p. 676-679 4 p.

Research output: Contribution to journalArticle

Scoliosis
G-Protein-Coupled Receptors
Genome-Wide Association Study
Single Nucleotide Polymorphism
Chromosomes
5 Citations (Scopus)

Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error

Kim, W., Londono, D., Zhou, L., Xing, J., Nato, A. Q., Musolf, A., Matise, T., Finch, S. J. & Gordon, D., Apr 1 2013, In : Human Heredity. 74, 3-4, p. 172-183 12 p.

Research output: Contribution to journalArticle

Single Nucleotide Polymorphism
Technology
Genome
Internal-External Control
Economic Inflation
2012
12 Citations (Scopus)

IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

Floros, J., Londono, D., Gordon, D., Silveyra, P., Diangelo, S. L., Viscardi, R. M., Worthen, G. S., Shenberger, J., Wang, G., Lin, Z. & Thomas, N. J., Jan 1 2012, In : Pediatric Research. 71, 1, p. 107-114 8 p.

Research output: Contribution to journalArticle

Bronchopulmonary Dysplasia
African Americans
Single Nucleotide Polymorphism
Infant, Newborn, Diseases
Genetic Association Studies
6 Citations (Scopus)

TDT-HET: A new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

Londono, D., Buyske, S., Finch, S. J., Sharma, S., Wise, C. A. & Gordon, D., Jan 20 2012, In : BMC Bioinformatics. 13, 1, 13.

Research output: Contribution to journalArticle

Data Association
Locus
Statistics
Proportion
Genetic Phenomena
2011
4 Citations (Scopus)

A new expectation-maximization statistical test for case-control association studies considering rare variants obtained by high-throughput sequencing

Gordon, D., Finch, S. J. & De La Vega, F., Jul 1 2011, In : Human Heredity. 71, 2, p. 113-125 13 p.

Research output: Contribution to journalArticle

Case-Control Studies
Genome-Wide Association Study
Base Pairing
Single Nucleotide Polymorphism
Meta-Analysis
105 Citations (Scopus)

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes

Sharma, S., Gao, X., Londono, D., Devroy, S. E., Mauldin, K. N., Frankel, J. T., Brandon, J. M., Zhang, D., Li, Q. Z., Dobbs, M. B., Gurnett, C. A., Grant, S. F. A., Hakonarson, H., Dormans, J. P., Herring, J. A., Gordon, D. & Wise, C. A., Apr 1 2011, In : Human molecular genetics. 20, 7, p. 1456-1466 11 p., ddq571.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Scoliosis
Single Nucleotide Polymorphism
Genes
Chromosomes
2010
4 Citations (Scopus)

A Cost-effective statistical method to correct for differential genotype misclassification when performing case-control genetic association

Londono, D., Haynes, C., De La Vega, F. M., Finch, S. J. & Gordon, D., Jul 1 2010, In : Human Heredity. 70, 2, p. 102-108 7 p.

Research output: Contribution to journalArticle

Genotype
Costs and Cost Analysis
Genome-Wide Association Study
Genetic Models
Population
2009

Computing power of quantitative trait locus association mapping for haploid loci

Gordon, D. & Zinn, A. R., Aug 23 2009, In : BMC Bioinformatics. 10, 261.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Haploidy
Locus
Computing
Biometrics
19 Citations (Scopus)
Case-control Study
Homozygote
Rejection
Gene Frequency
Error Rate
15 Citations (Scopus)

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+

Poduri, A., Wang, Y., Gordon, D., Barral-Rodriguez, S., Barker-Cummings, C., Ulgen, A., Chitsazzadeh, V., Hill, R. S., Risch, N., Hauser, W. A., Pedley, T. A., Walsh, C. A. & Ottman, R., 2009, In : Neurology. 73, 16, p. 1264-1272 9 p.

Research output: Contribution to journalArticle

Febrile Seizures
Epilepsy
Chromosomes
Genes
Lod Score
5 Citations (Scopus)

The cost effectiveness of duplicate genotyping for testing genetic association

Tintle, N., Gordon, D., Van Bruggen, D. & Finch, S., May 8 2009, In : Annals of Human Genetics. 73, 3, p. 370-378 9 p.

Research output: Contribution to journalArticle

Genetic Testing
Cost-Benefit Analysis
Costs and Cost Analysis
Single Nucleotide Polymorphism
Genome-Wide Association Study
5 Citations (Scopus)
Sample Size
Locus
Association reactions
Genes
Chromosome Mapping
18 Citations (Scopus)
Sample Size
Phenotype
Genetic Association Studies
Power (Psychology)
Software
2008
7 Citations (Scopus)

A family-based likelihood ratio test for general pedigree structures that allows for genotyping error and missing data

Yang, Y., Wise, C. A., Gordon, D. & Finch, S. J., Mar 1 2008, In : Human Heredity. 66, 2, p. 99-110 12 p.

Research output: Contribution to journalArticle

Pedigree
Genotype
Likelihood Functions
Penetrance
Scoliosis
27 Citations (Scopus)

Catechol-O-methyltransferase (COMT) gene variants: Possible association of the Val158Met variant with opiate addiction in hispanic women

Oosterhuis, B. E., LaForge, K. S., Proudnikov, D., Ho, A., Nielsen, D. A., Gianotti, R., Barral, S., Gordon, D., Leal, S. M., Ott, J. & Kreek, M. J., Sep 5 2008, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147, 6, p. 793-798 6 p.

Research output: Contribution to journalArticle

Opioid-Related Disorders
Catechol O-Methyltransferase
Hispanic Americans
Single Nucleotide Polymorphism
Genotype
12 Citations (Scopus)

Computing power and sample size for case-control association studies with copy number polymorphism: Application of mixture-based likelihood ratio test

Kim, W., Gordon, D., Sebat, J., Ye, K. Q. & Finch, S. J., Oct 22 2008, In : PloS one. 3, 10, e3475.

Research output: Contribution to journalArticle

DNA Copy Number Variations
Polymorphism
polymorphism
Sample Size
Case-Control Studies
148 Citations (Scopus)

Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair

Shimomura, Y., Wajid, M., Ishii, Y., Shapiro, L., Petukhova, L., Gordon, D. & Christiano, A. M., Mar 1 2008, In : Nature genetics. 40, 3, p. 335-339 5 p.

Research output: Contribution to journalArticle

G-Protein-Coupled Receptors
Hair
Nested Genes
Retinoblastoma Genes
Genetic Databases
20 Citations (Scopus)

Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation

Petukhova, L., Sousa, E. C., Martinez-Mir, A., Vitebsky, A., dos Santos, L. G., Shapiro, L., Haynes, C., Gordon, D., Shimomura, Y. & Christiano, A. M., Nov 1 2008, In : Genomics. 92, 5, p. 273-278 6 p.

Research output: Contribution to journalArticle

Genome
Mutation
Lod Score
Genes
Hypotrichosis
39 Citations (Scopus)

Telomerase levels in schizophrenia: A preliminary study

Porton, B., DeLisi, L. E., Bertisch, H. C., Ji, F., Gordon, D., Li, P., Benedict, M. M., Greenberg, W. M. & Kao, H. T., Dec 1 2008, In : Schizophrenia Research. 106, 2-3, p. 242-247 6 p.

Research output: Contribution to journalArticle

Telomerase
Schizophrenia
Telomere
Lymphocytes
2007
102 Citations (Scopus)

CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis

Gao, X., Gordon, D., Zhang, D., Browne, R., Helms, C., Gillum, J., Weber, S., Devroy, S., Swaney, S., Dobbs, M., Morcuende, J., Sheffield, V., Lovett, M., Bowcock, A., Herring, J. & Wise, C., Jan 1 2007, In : American Journal of Human Genetics. 80, 5, p. 957-965 9 p.

Research output: Contribution to journalArticle

Scoliosis
Genes
Exons
CHARGE Syndrome
Coloboma
99 Citations (Scopus)

Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata

Martinez-Mir, A., Zlotogorski, A., Gordon, D., Petukhova, L., Mo, J., Gilliam, T. C., Londono, D., Haynes, C., Ott, J., Hordinsky, M., Nanova, K., Norris, D., Price, V., Duvic, M. & Christiano, A. M., Jan 1 2007, In : American Journal of Human Genetics. 80, 2, p. 316-328 13 p.

Research output: Contribution to journalArticle

Alopecia Areata
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 16
Hair
Chromosomes
4 Citations (Scopus)

Incorporation of genetic model parameters for cost-effective designs of genetic association studies using DNA pooling

Ji, F., Finch, S. J., Haynes, C., Mendell, N. R. & Gordon, D., Jul 16 2007, In : BMC genomics. 8, 238.

Research output: Contribution to journalArticle

Genetic Models
Genetic Association Studies
Single Nucleotide Polymorphism
Costs and Cost Analysis
DNA
22 Citations (Scopus)

Linear trend tests for case-control genetic association that incorporate random phenotype and genotype misclassification error

Gordon, D., Haynes, C., Yang, Y., Kramer, P. L. & Finch, S. J., Dec 1 2007, In : Genetic Epidemiology. 31, 8, p. 853-870 18 p.

Research output: Contribution to journalArticle

Genotype
Phenotype
Alzheimer Disease
Penetrance
Apolipoproteins E
37 Citations (Scopus)

Prodynorphin gene promoter repeat associated with cocaine/alcohol codependence

Williams, T. J., LaForge, K. S., Gordon, D., Bart, G., Kellogg, S., Ott, J. & Kreek, M. J., Sep 1 2007, In : Addiction Biology. 12, 3-4, p. 496-502 7 p.

Research output: Contribution to journalArticle

Cocaine
Genotype
Alcohols
African Americans
Substance-Related Disorders
7 Citations (Scopus)

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations

Brown, A. M., Gordon, D., Lee, H., Vrièze, F. W. D., Cellini, E., Bagnoli, S., Nacmias, B., Sorbi, S., Hardy, J. & Blass, J. P., Apr 1 2007, In : Neurochemical Research. 32, 4-5, p. 857-869 13 p.

Research output: Contribution to journalArticle

Dihydrolipoamide Dehydrogenase
Alzheimer Disease
Genes
National Institute of Mental Health (U.S.)
Testing
28 Citations (Scopus)

The effects of SNP genotyping errors on the power of the cochran-armitage linear trend test for case/control association studies

Ahn, K., Haynes, C., Kim, W., St. Fleur, R., Gordon, D. & Finch, S. J., Mar 1 2007, In : Annals of Human Genetics. 71, 2, p. 249-261 13 p.

Research output: Contribution to journalArticle

Homozygote
Single Nucleotide Polymorphism
Case-Control Studies
Sample Size
Genetic Models
8 Citations (Scopus)

The impact of genotype misclassification errors on the power to detect a gene-environment interaction using cox proportional hazards modeling

Tung, L., Gordon, D. & Finch, S. J., Feb 1 2007, In : Human Heredity. 63, 2, p. 101-110 10 p.

Research output: Contribution to journalArticle

Gene-Environment Interaction
Sample Size
Genotype
Gene Frequency
Genes
17 Citations (Scopus)

Using duplicate genotyped data in genetic analyses: Testing association and estimating error rates

Tintle, N. L., Gordon, D., McMahon, F. J. & Finch, S. J., Feb 5 2007, In : Statistical Applications in Genetics and Molecular Biology. 6, 1, 4.

Research output: Contribution to journalArticle

Genetic Testing
Analysis of variance (ANOVA)
Error Rate
Analysis of Variance
Multivariate Analysis
2006
13 Citations (Scopus)

A detailed hapmap of the sitosterolemia locus spanning 69 kb; differences between Caucasians and African-Americans

Pandit, B., Ahn, G. S., Hazard, S. E., Gordon, D. & Patel, S. B., Feb 28 2006, In : BMC Medical Genetics. 7, 13.

Research output: Contribution to journalArticle

HapMap Project
African Americans
Single Nucleotide Polymorphism
Haplotypes
Linkage Disequilibrium
17 Citations (Scopus)

Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes

Levenstien, M. A., Ott, J. & Gordon, D., Sep 4 2006, In : PLoS genetics. 2, 8, p. 1156-1166 11 p.

Research output: Contribution to journalArticle

Haplotypes
haplotypes
Costs and Cost Analysis
genotype
cost
42 Citations (Scopus)

Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: A comparison of molecular and statistically estimated haplotypes

Proudnikov, D., LaForge, K. S., Hofflich, H., Levenstien, M., Gordon, D., Barral, S., Ott, J. & Kreek, M. J., Jan 1 2006, In : Pharmacogenetics and Genomics. 16, 1, p. 25-36 12 p.

Research output: Contribution to journalArticle

Receptor, Serotonin, 5-HT1B
Heroin Dependence
Haplotypes
Genes
Alleles
19 Citations (Scopus)
Misclassification Error
Genetic Association
Asymptotic Power
Case-control
Genetic Association Studies
57 Citations (Scopus)

Disease Relevant HLA Class II Alleles Isolated by Genotypic, Haplotypic, and Sequence Analysis in North American Caucasians With Pemphigus Vulgaris

Lee, E., Lendas, K. A., Chow, S., Pirani, Y., Gordon, D., Dionisio, R., Nguyen, D., Spizuoco, A., Fotino, M., Zhang, Y. & Sinha, A. A., Jan 1 2006, In : Human Immunology. 67, 1-2, p. 125-139 15 p.

Research output: Contribution to journalArticle

Pemphigus
HLA Antigens
Sequence Analysis
Alleles
Linkage Disequilibrium
7 Citations (Scopus)
National Institute of Mental Health (U.S.)
Pedigree
Gold
Alzheimer Disease
Autopsy
14 Citations (Scopus)

Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping

Ellis, N. A., Kirchhoff, T., Mitra, N., Ye, T. Z., Chuai, S., Huang, H., Nafa, K., Norton, L., Neuhausen, S., Gordon, D., Struewing, J. P., Narod, S. & Offit, K., Jan 1 2006, In : Genetic Epidemiology. 30, 1, p. 48-61 14 p.

Research output: Contribution to journalArticle

Chromosome Mapping
Linkage Disequilibrium
Single Nucleotide Polymorphism
Genome
Breast Neoplasms
10 Citations (Scopus)

LRTae: Improving statistical power for genetic association with case/control data when phenotype and/or genotype misclassification errors are present

Barral, S., Haynes, C., Stone, M. & Gordon, D., Apr 27 2006, In : BMC genetics. 7, 24.

Research output: Contribution to journalArticle

Genotype
Phenotype
Haplotypes
Case-Control Studies
Ankylosing Spondylitis
2005
18 Citations (Scopus)

Characteristics of replicated single-nucleotide polymorphism genotypes from COGA: Affymetrix and Center for Inherited Disease Research

Tintle, N. L., Ahn, K., Mendell, N. R., Gordon, D. & Finch, S. J., Dec 30 2005, In : BMC genetics. 6, SUPPL.1, S154.

Research output: Contribution to journalArticle

Single Nucleotide Polymorphism
Genotype
Research
Genetic Databases
Alcoholism
38 Citations (Scopus)

Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata.

Chuang, G. S., Martinez-Mir, A., Geyer, A., Engler, D. E., Glaser, B., Cserhalmi-Friedman, P. B., Gordon, D., Horev, L., Lukash, B., Herman, E., Cid, M. P., Brenner, S., Landau, M., Sprecher, E., Garcia Muret, M. P., Christiano, A. M. & Zlotogorski, A., Jan 1 2005, In : Journal of the American Academy of Dermatology. 52, 3 Pt 1, p. 410-416 7 p.

Research output: Contribution to journalArticle

Fumarate Hydratase
Leiomyoma
Mutation
Genes
Smooth Muscle Tumor
86 Citations (Scopus)

Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders

Frishberg, Y., Topaz, O., Bergman, R., Behar, D., Fisher, D., Gordon, D., Richard, G. & Sprecher, E., Jan 1 2005, In : Journal of Molecular Medicine. 83, 1, p. 33-38 6 p.

Research output: Contribution to journalArticle

Calcinosis
Mutation
Hyperphosphatemic Familial Tumoral Calcinosis
Hyperostosis-hyperphosphatemia syndrome
Hyperostosis
55 Citations (Scopus)

Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR

Helms, C., Saccone, N. L., Cao, L., Wright Daw, J. A., Cao, K., Hsu, T. M., Taillon-Miller, P., Duan, S., Gordon, D., Pierce, B., Ott, J., Rice, J., Fernandez-Vina, M. A., Kwok, P. Y., Menter, A. & Bowcock, A. M., Dec 1 2005, In : Human Genetics. 118, 3-4, p. 466-476 11 p.

Research output: Contribution to journalArticle

HLA-C Antigens
Haplotypes
Alleles
Single Nucleotide Polymorphism
Linkage Disequilibrium