1 - 25 of 124 results for author:"Martin N.G." in Literature citations
Results Customize
› Repeat search in UniProtKB (13)
| Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses. Zhang K., Rao F., Miramontes-Gonzalez J.P., Hightower C.M., Vaught B., Chen Y., Greenwood T.A., Schork A.J., Wang L., Mahata M. et al. J. Am. Coll. Cardiol. 60:1678-1689(2012) · Mapped (2) |
| Genetic variants near PDGFRA are associated with corneal curvature in Australians. Mishra A., Yazar S., Hewitt A.W., Mountain J.A., Ang W., Pennell C.E., Martin N.G., Montgomery G.W., Hammond C.J., Young T.L. et al. Invest. Ophthalmol. Vis. Sci. 53:7131-7136(2012) · Mapped (1) |
| Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Hartz S.M., Short S.E., Saccone N.L., Culverhouse R., Chen L., Schwantes-An T.H., Coon H., Han Y., Stephens S.H., Sun J. et al. Arch. Gen. Psychiatry 69:854-860(2012) · Mapped (3) |
| Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins. Hibar D.P., Jahanshad N., Stein J.L., Kohannim O., Toga A.W., Medland S.E., Hansell N.K., McMahon K.L., de Zubicaray G.I., Montgomery G.W. et al. Twin Res Hum Genet 15:286-295(2012) · Mapped (1) |
| A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Byrne E.M., Johnson J., McRae A.F., Nyholt D.R., Medland S.E., Gehrman P.R., Heath A.C., Madden P.A., Montgomery G.W., Chenevix-Trench G. et al. Sleep 35:967-975(2012) · Mapped (4) |
| Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults. Braskie M.N., Jahanshad N., Stein J.L., Barysheva M., Johnson K., McMahon K.L., de Zubicaray G.I., Martin N.G., Wright M.J., Ringman J.M. et al. J. Neurosci. 32:5964-5972(2012) · Mapped (2) |
| Common variants at 12q14 and 12q24 are associated with hippocampal volume. Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium Nat. Genet. 44:545-551(2012) · Mapped (7) |
| Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2. Dennis E.L., Jahanshad N., Rudie J.D., Brown J.A., Johnson K., McMahon K.L., de Zubicaray G.I., Montgomery G., Martin N.G., Wright M.J. et al. Brain Connect 1:447-459(2011) · Mapped (21) |
| Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene. Jahanshad N., Kohannim O., Hibar D.P., Stein J.L., McMahon K.L., de Zubicaray G.I., Medland S.E., Montgomery G.W., Whitfield J.B., Martin N.G. et al. Proc. Natl. Acad. Sci. U.S.A. 109:E851-9(2012) · Mapped (9) |
| Longevity candidate genes and their association with personality traits in the elderly. Luciano M., Lopez L.M., de Moor M.H., Harris S.E., Davies G., Nutile T., Krueger R.F., Esko T., Schlessinger D., Toshiko T. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 159B:192-200(2012) · Mapped (5) |
| New gene functions in megakaryopoiesis and platelet formation. Gieger C., Radhakrishnan A., Cvejic A., Tang W., Porcu E., Pistis G., Serbanovic-Canic J., Elling U., Goodall A.H., Labrune Y. et al. Nature 480:201-208(2011) · Mapped (22) |
| A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Yokoyama S., Woods S.L., Boyle G.M., Aoude L.G., MacGregor S., Zismann V., Gartside M., Cust A.E., Haq R., Harland M. et al. |
| Loci affecting gamma-glutamyl transferase in adults and adolescents show age X SNP interaction and cardiometabolic disease associations. Middelberg R.P., Benyamin B., de Moor M.H., Warrington N.M., Gordon S., Henders A.K., Medland S.E., Nyholt D.R., de Geus E.J., Hottenga J.J. et al. Hum. Mol. Genet. 21:446-455(2012) · Mapped (9) |
| Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma. Kvaskoff M., Whiteman D.C., Zhao Z.Z., Montgomery G.W., Martin N.G., Hayward N.K., Duffy D.L. Twin Res Hum Genet 14:422-432(2011) · Mapped (8) |
| Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning. Luong H.T., Chaplin J., McRae A.F., Medland S.E., Willemsen G., Nyholt D.R., Henders A.K., Hoekstra C., Duffy D.L., Martin N.G. et al. Twin Res Hum Genet 14:408-416(2011) · Mapped (4) |
| Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. Middelberg R.P., Ferreira M.A., Henders A.K., Heath A.C., Madden P.A., Montgomery G.W., Martin N.G., Whitfield J.B. BMC Med. Genet. 12:123-123(2011) · Mapped (25) |
| Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins. Rao F., Chiron S., Wei Z., Fung M.M., Chen Y., Wen G., Khandrika S., Ziegler M.G., Benyamin B., Montgomery G. et al. Am. J. Hypertens. 25:29-40(2012) · Mapped (3) |
| Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Australian Asthma Genetics Consortium Lancet 378:1006-1014(2011) · Mapped (3) |
| GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Benyamin B., Middelberg R.P., Lind P.A., Valle A.M., Gordon S., Nyholt D.R., Medland S.E., Henders A.K., Heath A.C., Madden P.A. et al. Hum. Mol. Genet. 20:4504-4514(2011) · Mapped (3) |
| The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin. Martin N.G., Li K.W., Murray H., Putt W., Packard C.J., Humphries S.E. Br J Clin Pharmacol 73:303-306(2012) · Mapped (5) |
| Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. Kutalik Z., Benyamin B., Bergmann S., Mooser V., Waeber G., Montgomery G.W., Martin N.G., Madden P.A., Heath A.C., Beckmann J.S. et al. Hum. Mol. Genet. 20:3710-3717(2011) · Mapped (9) |
| Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. COGENT Consortium PLoS Genet. 7:e1002105-e1002105(2011) · Mapped (8) |
| Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults. Braskie M.N., Jahanshad N., Stein J.L., Barysheva M., McMahon K.L., de Zubicaray G.I., Martin N.G., Wright M.J., Ringman J.M., Toga A.W. et al. J. Neurosci. 31:6764-6770(2011) · Mapped (5) |
| Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Burdon K.P., Macgregor S., Hewitt A.W., Sharma S., Chidlow G., Mills R.A., Danoy P., Casson R., Viswanathan A.C., Liu J.Z. et al. Nat. Genet. 43:574-578(2011) · Mapped (5) |
| Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Stein J.L., Hibar D.P., Madsen S.K., Khamis M., McMahon K.L., de Zubicaray G.I., Hansell N.K., Montgomery G.W., Martin N.G., Wright M.J. et al. Mol. Psychiatry 16:927-37, 2011:881-881(2011) · Mapped (6) |