Browse by Publication

12

Lange, NE and Zhou, X and Lasky-Su, J and Himes, BE and Lazarus, R and Soto-Quirós, M and Avila, L and Celedón, JC and Hawrylowicz, CM and Raby, BA and Litonjua, AA (2011) Comprehensive genetic assessment of a functional TLR9 promoter polymorphism: No replicable association with asthma or asthma-related phenotypes. BMC Medical Genetics, 12.

Lillvis, JH and Kyo, Y and Tromp, G and Lenk, GM and Li, M and Lu, Q and Igo, RP and Sakalihasan, N and Ferrell, RE and Schworer, CM and Gatalica, Z and Land, S and Kuivaniemi, H (2011) Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19. BMC Medical Genetics, 12.

He, C and Weeks, DE and Buyske, S and Abecasis, GR and Stewart, WC and Matise, TC (2011) Enhanced genetic maps from family-based disease studies: Population-specific comparisons. BMC Medical Genetics, 12.

Dasgupta, S and Demirci, FY and Dressen, AS and Kao, AH and Rhew, EY and Ramsey-Goldman, R and Manzi, S and Kammerer, CM and Kamboh, MI (2011) Association analysis of PON2 genetic variants with serum paraoxonase activity and systemic lupus erythematosus. BMC Medical Genetics, 12.

13

Rajkumar, Revathi and Sembrat, John C and McDonough, Barbara and Seidman, Christine E and Ahmad, Ferhaan (2012) Functional effects of the TMEM43 Ser358Leu mutation in the pathogenesis of arrhythmogenic right ventricular cardiomyopathy. BMC Medical Genetics, 13 (1).

14

Küchler, EC and Deeley, K and Ho, B and Linkowski, S and Meyer, C and Noel, J and Kouzbari, MZ and Bezamat, M and Granjeiro, JM and Antunes, LS and Antunes, LA and de Abreu, FV and Costa, MC and Tannure, PN and Seymen, F and Koruyucu, M and Patir, A and Mereb, JC and Poletta, FA and Castilla, EE and Orioli, IM and Marazita, ML and Vieira, AR (2013) Genetic mapping of high caries experience on human chromosome 13. BMC Medical Genetics, 14 (1).

Kim, J and Stirling, KJ and Cooper, ME and Ascoli, M and Momany, AM and McDonald, EL and Ryckman, KK and Rhea, L and Schaa, KL and Cosentino, V and Gadow, E and Saleme, C and Shi, M and Hallman, M and Plunkett, J and Teramo, KA and Muglia, LJ and Feenstra, B and Geller, F and Boyd, HA and Melbye, M and Marazita, ML and Dagle, JM and Murray, JC (2013) Sequence variants in oxytocin pathway genes and preterm birth: A candidate gene association study. BMC Medical Genetics, 14 (1).

Fesinmeyer, MD and North, KE and Lim, U and Bůžková, P and Crawford, DC and Haessler, J and Gross, MD and Fowke, JH and Goodloe, R and Love, SA and Graff, M and Carlson, CS and Kuller, LH and Matise, TC and Hong, CP and Henderson, BE and Allen, M and Rohde, RR and Mayo, P and Schnetz-Boutaud, N and Monroe, KR and Ritchie, MD and Prentice, RL and Kolonel, LN and Manson, JAE and Pankow, J and Hindorff, LA and Franceschini, N and Wilkens, LR and Haiman, CA and Le Marchand, L and Peters, U (2013) Effects of smoking on the genetic risk of obesity: The population architecture using genomics and epidemiology study. BMC Medical Genetics, 14 (1).

15

Weber, ML and Hsin, HY and Kalay, E and Brožková, DT and Shimizu, T and Bayram, M and Deeley, K and Küchler, EC and Forella, J and Ruff, TD and Trombetta, VM and Sencak, RC and Hummel, M and Briseño-Ruiz, J and Revu, SK and Granjeiro, JM and Antunes, LS and Antunes, LA and Abreu, FV and Costa, MC and Tannure, PN and Koruyucu, M and Patir, A and Poletta, FA and Mereb, JC and Castilla, EE and Orioli, IM and Marazita, ML and Ouyang, H and Jayaraman, T and Seymen, F and Vieira, AR (2014) Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay. BMC Medical Genetics, 15 (1).

16

Niemsiri, V and Wang, X and Pirim, D and Radwan, ZH and Bunker, CH and Barmada, MM and Kamboh, MI and Demirci, FY (2015) Genetic contribution of SCARB1 variants to lipid traits in African Blacks: A candidate gene association study. BMC Medical Genetics, 16 (1).

Mancini, C and Orsi, L and Guo, Y and Li, J and Chen, Y and Wang, F and Tian, L and Liu, X and Zhang, J and Jiang, H and Nmezi, BS and Tatsuta, T and Giorgio, E and Di Gregorio, E and Cavalieri, S and Pozzi, E and Mortara, P and Caglio, MM and Balducci, A and Pinessi, L and Langer, T and Padiath, QS and Hakonarson, H and Zhang, X and Brusco, A (2015) An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2. BMC Medical Genetics, 16 (1).