HuGE Literature Finder
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The SNP rs7865618 of 9p21.3 locus emerges as the most promising marker of coronary artery disease in the southern Indian population. Scientific reports 2020 Dec 10 (1): 21511. Manjula Gorre, Pranavchand Rayabarapu, Kumuda Irgam, Reddy B Sriteja, Reddy Battini Moh |
Impact of variants on type-2 diabetes risk genes identified through genomewide association studies in polycystic ovary syndrome: a case-control study. Journal of genetics 2018 Dec 97 (5): 1213-1223. Ezzidi Intissar, Mtiraoui Nabil, Mohmmed Ali Mohammed Eltigani, Masoudi Aqeel Al, Abu Duhier Fais |
Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1. Journal of the National Cancer Institute 2011 Nov 103 (22): 1713-22. Pasmant Eric, Sabbagh Audrey, Masliah-Planchon Julien, Ortonne Nicolas, Laurendeau Ingrid, Melin Lucie, Ferkal Salah, Hernandez Lucie, Leroy Karen, Valeyrie-Allanore Laurence, Parfait Béatrice, Vidaud Dominique, Bièche Ivan, Lantieri Laurent, Wolkenstein Pierre, Vidaud Michel, |
Genetic variants in the cell cycle control pathways contribute to early onset colorectal cancer in Lynch syndrome. Cancer causes & control : CCC 2009 Nov 20 (9): 1769-77. Chen Jinyun, Etzel Carol J, Amos Christopher I, Zhang Qing, Viscofsky Nancy, Lindor Noralane M, Lynch Patrick M, Frazier Marsha |
Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype. Haematologica 2009 Feb 94 (2): 213-23. Akagi Tadayuki, Ogawa Seishi, Dugas Martin, Kawamata Norihiko, Yamamoto Go, Nannya Yasuhito, Sanada Masashi, Miller Carl W, Yung Amanda, Schnittger Susanne, Haferlach Torsten, Haferlach Claudia, Koeffler H Phill |
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