• 3935 Citations
  • 36 h-Index
1990 …2019

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2019
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

1 Scopus citations

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

6 Scopus citations
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

2015

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

64 Scopus citations

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

11 Scopus citations
2014

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

37 Scopus citations

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

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

Research output: Contribution to journalArticle

6 Scopus citations

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

10 Scopus citations
2013

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

28 Scopus citations

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. C. & 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

10 Scopus citations

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

120 Scopus citations

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. C., Finch, S. J. & Gordon, D., Apr 1 2013, In : Human Heredity. 74, 3-4, p. 172-183 12 p.

Research output: Contribution to journalArticle

6 Scopus citations
2012

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

12 Scopus citations

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

6 Scopus citations
2011

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

5 Scopus citations

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

109 Scopus citations
2010

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

4 Scopus citations
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

19 Scopus citations

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

15 Scopus citations

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

6 Scopus citations
5 Scopus citations
21 Scopus citations
2008

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

7 Scopus citations

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

29 Scopus citations

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

13 Scopus citations

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

152 Scopus citations

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

20 Scopus citations

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

39 Scopus citations
2007

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., May 2007, In : American Journal of Human Genetics. 80, 5, p. 957-965 9 p.

Research output: Contribution to journalArticle

104 Scopus citations

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., Feb 2007, In : American Journal of Human Genetics. 80, 2, p. 316-328 13 p.

Research output: Contribution to journalArticle

101 Scopus citations

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

4 Scopus citations

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

24 Scopus citations

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

37 Scopus citations

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

7 Scopus citations

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

29 Scopus citations

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

8 Scopus citations

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

17 Scopus citations
2006

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

13 Scopus citations

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

18 Scopus citations

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

42 Scopus citations
21 Scopus citations

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

58 Scopus citations
7 Scopus citations

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

14 Scopus citations

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

12 Scopus citations
2005

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

18 Scopus citations

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., Mar 2005, In : Journal of the American Academy of Dermatology. 52, 3 Pt 1, p. 410-416 7 p.

Research output: Contribution to journalArticle

38 Scopus citations

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 2005, In : Journal of Molecular Medicine. 83, 1, p. 33-38 6 p.

Research output: Contribution to journalArticle

86 Scopus citations