B M C Medical Genetics
Collection
Collection
- ISSN: 14712350
Published by BMC - BioMed Central, London
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The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project Article
B M C Medical Genetics, 11(1)O. Combarros (Onofre), D.R. Warden (Donald), N. Hammond (Naomi), M. Cortina-Borja (Mario), O. Belbin (Olivia), M.G. Lehmann (Michael), G.K. Wilcock (Gordon), K. Brown (Kristelle), P.G. Kehoe (Patrick), R. Barber (Rachel), et al. E. Coto (Eliecer), V. Alvarez (Victoria), P. Deloukas (Panagiotis), R. Gwilliam (Rhian), R. Heun (Reinhard), H. Kölsch (Heike), I. Mateo (Ignacio), A. Oulhaj (Abderrahim), A. Arias-Vásquez (Alejandro), M. Schuur (Maaike), Y.S. Aulchenko (Yurii), M.A. Ikram (Arfan), M.M.B. Breteler (Monique), C.M. van Duijn (Cornelia), K. Morgan (Kevin) and A.D. Smith (David)
November 2010
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Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: Results of a meta-analysis Article
B M C Medical Genetics, 11(1)J.M. Kerkhof (Hanneke), I. Meulenbelt (Ingrid), A. Gonzalez (Antonio), D.J. Hart (Deborah), A. Hofman (Albert), M. Kloppenburg (Margreet), N.E. Lane, J. Loughlin (John), M.C. Nevitt (Michael), H.A.P. Pols (Huib), et al. F. Rivadeneira Ramirez (Fernando), P.E. Slagboom (Eline), T.D. Spector (Timothy), L. Stolk (Lisette), A. Tsezou (Aspasia), A.G. Uitterlinden (André), A.M. Valdes (Ana Maria), J.B.J. van Meurs (Joyce) and A.J. Carr (Andrew Jonathan)
November 2010
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Polymorphisms in genes controlling inflammation and tissue repair in rheumatoid arthritis: A case control study Article
B M C Medical GeneticsM. Emonts (Marieke), J.M.W. Hazes (Mieke), J.J. Houwing-Duistermaat (Jeanine), C.E. de Jongh (Christa), L. de Vogel (Lisette), K.H. Han (Hubert), J.M.G.W. Wouters (Jacques), J.D. Laman (Jon) and R.J.E.M. Dolhain (Radboud)
March 2011
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A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease Article
B M C Medical GeneticsP. Sanchez-Juan (Pascual), M.T. Bishop (Matthew), E.A. Croes (Esther), R.S.G. Knight (Richard), R.G. Will, P. Tikka-Kleemola (Päivi) and J.C. Manson (Jean)
May 2011
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SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype Article
B M C Medical GeneticsR. Hersmus (Remko), J.A. Stoop (Hans), E. Turbitt (Erin), J.W. Oosterhuis (Wolter), S.L.S. Drop (Stenvert), A. Sinclair (Andrew), S.J. White (Stefan) and L.H.J. Looijenga (Leendert)
November 2012
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Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes Article
B M C Medical Genetics, 14(1)N.V. Rivera (Natalia), R. Carreras-Torres (Robert), R. Roncarati (Roberta), C. Viviani-Anselmi (Chiara), F. de Micco (Francesca), A. Mezzelani (Alessandra), W. Koch (Werner), P. Hoppmann (Petra), A. Kastrati (Adnan), A.F.R. Stewart (Alexandre), et al. L. Chen (Leslie), R. Roberts (Robert), L.C. Karssen (Lennart), N. Amin (Najaf), V. Trimarco (Valentina), R. Izzo (Raffaele), G. Iaccarino (Guido), G. Condorelli (Gerolama), A.A. Puca (Annibale), P. Pagnotta (Paolo), F. Airoldi (Flavio), B. Trimarco (Bruno), C.M. van Duijn (Cornelia), G. Condorelli (Gianluigi) and C. Briguori (Carlo)
January 2013
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Genetics of coronary artery calcification among African Americans, a meta-analysis Article
B M C Medical Genetics, 14(1)M.K. Wojczynski (Mary ), M. Li (Mingyao), L.F. Bielak (Lawrence F.), K.F. Kerr (Kathleen), A. Reiner (Alexander), N.D. Wong (Nathan), L.R. Yanek (Lisa), L. Qu (Liming), C.C. White (Charles), L.A. Lange (Leslie), et al. J.F. Ferguson (Jane), J. He (Jing), T. Young (Taylor), T.H. Mosley (Thomas), J.A. Smith (Jennifer A), B.G. Kral (Brian), X. Guo (Xiuqing), Q. Wong (Quenna), S.K. Ganesh (Santhi), S.R. Heckbert (Susan), M.D. Griswold (Michael), D.H. O'Leary (Daniel H.), M.J. Budoff (Matthew), J. Carr (Jeffrey), H.A. Taylor (Herman), D.A. Bluemke (David), S. Demissie (Serkalem), S.-J. Hwang (Shih-Jen), D.N. Paltoo (Dina), J.F. Polak (Joseph F.), B.M. Psaty (Bruce), D.M. Becker (Diane), M.A. Province (Mike), W.S. Post (Wendy S.), C.J. O'Donnell (Christopher), J.G. Wilson (James), T.B. Harris (Tamara), M. Kavousi (Maryam), L.A. Cupples (Adrienne), J.I. Rotter (Jerome), M. Fornage (Myriam), L.C. Becker (Lewis), P.A. Peyser (Patricia A.), I.B. Borecki (Ingrid) and M.P. Reilly (Muredach)
July 2013
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Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome Article
B M C Medical Genetics, 15(1)A.L. Fenwick (Aimée), J.A.C. Goos (Jacqueline), J. Rankin (Julia), H. Lord (Helen), K.J. Lester (Kathryn), A.J.M. Hoogeboom (Jeannette), A.M.W. van den Ouweland (Ans), S.A. Wall (Steven), I.M.J. Mathijssen (Irene) and A.O.M. Wilkie (Andrew)
August 2014