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Articles of Interest

• Selelstad, Mark T.; Hebert, Joan M.; Lin, Alice A.; UnderhllI, Peter A.; Ibrahlm, Muntaser; Vollrath, Douglas & Cavalll-Storza (1994). Construction of human Y-chromosomal haplotypes using a new polymorphic A to G transition. Human Molecular Genetics, 3(12), 2159-2161.
• Deckert, J A¼rgen; Catalano, Marco; Syagailo, Yana V.; Bosi, Monica; Okladnova, Olga; Di Bella, Daniela; N APthen, Markus M.; Maffei, Piermario; Franke, Petra; Fritze, J A¼rgen; Maier, Wolfgang; Propping, Peter; Beckmann, Helmut; Bellodi, Laura & Lesch, K (1999). Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder. Human Molecular Genetics, 8(4), 621-624.
• Conlin, Laura K.; Thiel, Brian D.; Bonnemann, Carsten G.; Medne, Livija; Ernst, Linda M.; Zackai, Elaine H.; Deardorff, Matthew A.; Krantz, Ian D.; Hakonarson, Hakon & Spinner, Nancy B. (2010). Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis. Human Molecular Genetics, 19(7), 1263-1275.
• Lu, Chuncheng; Zhang, Jie; Li, Yingchun; Xia, Yankai; Zhang, Feng; Wu, Bin; Wu, Wei; Ji, Guixiang; Gu, Aihua; Wang, Shoulin; Jin, Li & Wang, Xinru (2009). The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population. Human Molecular Genetics, 18(6), 1122-1130.
• Payne, Brendan A. I.; Wilson, Ian J.; Yu-Wai-Man, Patrick; Coxhead, Jonathan; Deehan, David; Horvath, Rita; Taylor, Robert W.; Samuels, David C.; Santibanez-Koref, Mauro & Chinnery, Patrick F. (2013). Universal heteroplasmy of human mitochondrial DNA. Human Molecular Genetics, 22(2), 384-390.
• D'aurelio, M., Vives-Bauza, C., Davidson, M.M. and Manfredi, G. (2010). Mitochondrial DNA background modifies the bioenergetics of NARP/MILS ATP6 mutant cells. Human Molecular Genetics, 19(2), 374-386.
• Gómez-Durán, A., Pacheu-Grau, D., López-Gallardo, E., Díez-Sánchez, C., Montoya, J., López-Pérez, M.J. and Ruiz-Pesini, E. (2010). Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups. Human Molecular Genetics, 19(17), 3343-3353.
• Ingman, M. and Gyllensten, U. (2007). Rate variation between mitochondrial domains and adaptive evolution in humans. Human Molecular Genetics, 16(19), 2281-2287.
• Kong, Q.P., Bandelt, H.J., Sun, C., Yao, Y.G., Salas, A., Achilli, A., Wang, C.Y., Zhong, L., Zhu, C.L., Wu, S.F. and Torroni, A. (2006). Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations. Human Molecular Genetics, 15(13), 2076-2086.
• Pello, R., Martín, M.A., Carelli, V., Nijtmans, L.G., Achilli, A., Pala, M., Torroni, A., Gómez-Durán, A., Ruiz-Pesini, E., Martinuzzi, A. and Smeitink, J.A. (2008). Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease. Human Molecular Genetics, 17(24), 4001-4011.
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