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HyungChul Rah, Ph.D. - Publications

Affiliations: 
2006 University of California, Davis, Davis, CA 
Area:
Veterinary Science Biology, Genetics, Ophthalmology
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21 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Nilson SM, Gandolfi B, Grahn RA, Kurushima JD, Lipinski MJ, Randi E, Waly NE, Driscoll C, Escobar HM, Schuster RK, Maruyama S, Labarthe N, Chomel BB, Ghosh SK, Ozpinar H, ... Rah HC, et al. Genetics of randomly bred cats support the cradle of cat domestication being in the Near East. Heredity. PMID 36319737 DOI: 10.1038/s41437-022-00568-4  0.677
2016 Jang HG, Choi Y, Kim JO, Jeon YJ, Rah H, Cho SH, Kim JH, Lee WS, Kim NK. Polymorphisms in tumor necrosis factor-alpha (-863C>A, -857C>T and +488G>A) are associated with idiopathic recurrent pregnancy loss in Korean women. Human Immunology. PMID 27083536 DOI: 10.1016/J.Humimm.2016.04.012  0.313
2016 Lyons LA, Creighton EK, Alhaddad H, Beale HC, Grahn RA, Rah H, Maggs DJ, Helps CR, Gandolfi B. Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7. Bmc Genomics. 17: 265. PMID 27030474 DOI: 10.1186/S12864-016-2595-4  0.657
2015 Jung YW, Kim JO, Rah H, Kim JH, Kim YR, Lee Y, Lee WS, Kim NK. Genetic variants of vascular endothelial growth factor are associated with recurrent implantation failure in Korean women. Reproductive Biomedicine Online. PMID 26673101 DOI: 10.1016/J.Rbmo.2015.10.010  0.324
2014 Alhaddad H, Gandolfi B, Grahn RA, Rah HC, Peterson CB, Maggs DJ, Good KL, Pedersen NC, Lyons LA. Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 25: 354-62. PMID 24777202 DOI: 10.1007/S00335-014-9517-Z  0.693
2014 Lee KH, Rah H, Green T, Lee YK, Lim D, Nemzek J, Wahl W, Greenhalgh D, Cho K. Divergent and dynamic activity of endogenous retroviruses in burn patients and their inflammatory potential. Experimental and Molecular Pathology. 96: 178-87. PMID 24509167 DOI: 10.1016/J.Yexmp.2014.02.001  0.307
2014 Rah H, Jeon YJ, Ko JJ, Kim JH, Kim YR, Cha SH, Choi Y, Lee WS, Kim NK. Association of inhibin α gene promoter polymorphisms with risk of idiopathic primary ovarian insufficiency in Korean women. Maturitas. 77: 163-7. PMID 24269065 DOI: 10.1016/J.Maturitas.2013.10.015  0.318
2013 Jung YW, Jeon YJ, Park HM, Lee BE, Rah H, Lee WS, Yoon TK, Kim NK. Association between polymorphisms in renin-angiotensin system genes and primary ovarian insufficiency in Korean women. Menopause (New York, N.Y.). 20: 561-7. PMID 23615648 DOI: 10.1097/Gme.0B013E3182733921  0.309
2013 Rah H, Jeon YJ, Lee BE, Kim JO, Shim SH, Lee WS, Choi DH, Kim JH, Kim NK. Association of polymorphisms in microRNA machinery genes (DROSHA, DICER1, RAN, and XPO5) with risk of idiopathic primary ovarian insufficiency in Korean women. Menopause (New York, N.Y.). 20: 1067-73. PMID 23549446 DOI: 10.1097/Gme.0B013E3182883907  0.336
2013 Rah H, Jeon YJ, Lee BE, Choi DH, Yoon TK, Lee WS, Kim NK. Association of kinase insert domain-containing receptor (KDR) gene polymorphisms with idiopathic recurrent spontaneous abortion in Korean women. Fertility and Sterility. 99: 753-760.e8. PMID 23158831 DOI: 10.1016/J.Fertnstert.2012.10.038  0.31
2012 Rah H, Jeon YJ, Choi Y, Shim SH, Yoon TK, Choi DH, Cha SH, Kim NK. Association of methylenetetrahydrofolate reductase (MTHFR 677C>T) and thymidylate synthase (TSER and TS 1494del6) polymorphisms with premature ovarian failure in Korean women. Menopause (New York, N.Y.). 19: 1260-6. PMID 22713864 DOI: 10.1097/Gme.0B013E3182556B08  0.337
2012 Rah H, Choi YS, Jeon YJ, Choi Y, Cha SH, Choi DH, Ko JJ, Shim SH, Kim NK. Solute Carrier Family 19, member 1 (SLC19A1) polymorphisms (-43T>C, 80G>A, and 696C>T), and haplotypes in idiopathic recurrent spontaneous abortion in a Korean population. Reproductive Sciences (Thousand Oaks, Calif.). 19: 513-9. PMID 22344739 DOI: 10.1177/1933719111426604  0.32
2012 Jeon YJ, Choi YS, Rah H, Kim SY, Choi DH, Cha SH, Shin JE, Shim SH, Lee WS, Kim NK. Corrigendum to "Association study of microRNA polymorphisms with risk of idiopathic recurrent spontaneous abortion in Korean women" [Gene 494 (2012) 168-173] Gene. 498: 336. DOI: 10.1016/J.Gene.2012.02.012  0.33
2011 Jeon YJ, Kim JH, Rah H, Kim SY, Yoon TK, Choi DH, Cha SH, Shim SH, Kim NK. Vascular endothelial growth factor gene polymorphisms in spontaneously aborted fetuses. American Journal of Reproductive Immunology (New York, N.Y. : 1989). 66: 544-53. PMID 21902756 DOI: 10.1111/J.1600-0897.2011.01067.X  0.342
2011 Lee KH, Lee YK, Kwon DN, Chiu S, Chew V, Rah H, Kujawski G, Melhem R, Hsu K, Chung C, Greenhalgh DG, Cho K. Identification of a unique library of complex, but ordered, arrays of repetitive elements in the human genome and implication of their potential involvement in pathobiology. Experimental and Molecular Pathology. 90: 300-11. PMID 21376035 DOI: 10.1016/J.Yexmp.2011.02.007  0.338
2011 Jeon YJ, Choi YS, Rah HC, Choi Y, Yoon TK, Choi DH, Kim NK. The reduced folate carrier-1 (RFC1 696T>C) polymorphism is associated with spontaneously aborted embryos in Koreans Genes and Genomics. 33: 223-228. DOI: 10.1007/S13258-011-0016-2  0.342
2006 Lyons LA, Bailey SJ, Baysac KC, Byrns G, Erdman CA, Fretwell N, Froenicke L, Gazlay KW, Geary LA, Grahn JC, Grahn RA, Karere GM, Lipinski MJ, Rah H, Ruhe MT, et al. The Tabby cat locus maps to feline chromosome B1. Animal Genetics. 37: 383-6. PMID 16879352 DOI: 10.1111/J.1365-2052.2006.01458.X  0.673
2006 Rah H, Maggs DJ, Lyons LA. Lack of genetic association among coat colors, progressive retinal atrophy and polycystic kidney disease in Persian cats. Journal of Feline Medicine and Surgery. 8: 357-60. PMID 16777456 DOI: 10.1016/J.Jfms.2006.04.002  0.551
2005 Lyons LA, Foe IT, Rah HC, Grahn RA. Chocolate coated cats: TYRP1 mutations for brown color in domestic cats. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 356-66. PMID 16104383 DOI: 10.1007/S00335-004-2455-4  0.495
2005 Rah H, Maggs DJ, Blankenship TN, Narfstrom K, Lyons LA. Early-onset, autosomal recessive, progressive retinal atrophy in Persian cats. Investigative Ophthalmology & Visual Science. 46: 1742-7. PMID 15851577 DOI: 10.1167/Iovs.04-1019  0.551
2005 Lyons LA, Imes DL, Rah HC, Grahn RA. Tyrosinase mutations associated with Siamese and Burmese patterns in the domestic cat (Felis catus). Animal Genetics. 36: 119-26. PMID 15771720 DOI: 10.1111/J.1365-2052.2005.01253.X  0.488
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