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Palmer, ND and Kahali, B and Kuppa, A and Chen, Y and Du, X and Feitosa, MF and Bielak, LF and O'Connell, JR and Musani, SK and Guo, X and Smith, AV and Ryan, KA and Eirksdottir, G and Allison, MA and Bowden, DW and Budoff, MJ and Carr, JJ and Chen, Y-DI and Taylor, KD and Correa, A and Crudup, BF and Halligan, B and Yang, J and Kardia, SLR and Launer, LJ and Fu, Y-P and Mosley, TH and Norris, JM and Terry, JG and O'Donnell, CJ and Rotter, JI and Wagenknecht, LE and Gudnason, V and Province, MA and Peyser, PA and Speliotes, EK (2021) Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer's disease and myocardial infarction. In: Human Molecular Genetics, 30 (15). pp. 1443-1456.
Madhangi, M and Dutta, D and Show, S and Bhat, VK and Rather, MI and Tiwari, A and Singh, N and Duvvari, MR and Murthy, GJ and Kumar, A and Nongthomba, U (2021) Exome sequencing and functional studies in zebrafish identify WDR8 as the causative gene for isolated Microspherophakia in Indian families. In: Human Molecular Genetics, 30 (6). pp. 467-484.
Sinha, Devanjan and Joshi, Neha and Chittoor, Balasubramanyam and Samji, Priyanka and D'Silva, Patrick (2010) Role of Magmas in protein transport and human mitochondria biogenesis. In: Human Molecular Genetics, 19 (7). pp. 1248-1262.
Choudhry, Shweta and Mukerji, Mitali and Srivastava, Achal K and Jain, Satish and Brahmachari, Samir K (2001) CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms. In: Human Molecular Genetics, 10 (21). pp. 2437-2446.
Newbold, Richard J and Deery, Evelyne C and Walker, Caroline E and Wilkie, Susan E and Srinivasan, Narayanaswamy and Hunt, David M (2001) The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy. In: Human Molecular Genetics, 10 (1). pp. 47-54.
