Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("NALLS, Michael A")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 25

  • Page / 1
Export

Selection :

  • and

Impact of Ancestry and Common Genetic Variants on QT Interval in African AmericansGUSTAV SMITH, J; AVERY, Christy L; YOUNG, Taylor et al.Circulation. Cardiovascular genetics (Print). 2012, Vol 5, Num 6, pp 647-655, issn 1942-325X, 9 p.Article

Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP GeneCHIO, Adriano; BORGHERO, Giuseppe; RITA MURRU, Maria et al.Archives of neurology (Chicago). 2011, Vol 68, Num 5, pp 594-598, issn 0003-9942, 5 p.Article

Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individualsCORNEVEAUX, Jason J; MYERS, Amanda J; VILLA, Stephen E et al.Human molecular genetics (Print). 2010, Vol 19, Num 16, pp 3295-3301, issn 0964-6906, 7 p.Article

Imputation of Exome Sequence Variants into Population-Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing ProjectAUER, Paul L; JOHNSEN, Jill M; RICH, Stephen S et al.American journal of human genetics. 2012, Vol 91, Num 5, pp 794-808, issn 0002-9297, 15 p.Article

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseKELLER, Margaux F; SAAD, Mohamad; SCHULTE, Claudia et al.Human molecular genetics (Print). 2012, Vol 21, Num 22, pp 4996-5009, issn 0964-6906, 14 p.Article

Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function alleleTIN, Adrienne; WOODWARD, Owen M; HWANG, Shih-Jen et al.Human molecular genetics (Print). 2011, Vol 20, Num 20, pp 4056-4068, issn 0964-6906, 13 p.Article

Admixture Mapping of White Cell Count : Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart StudiesNALLS, Michael A; WILSON, James G; PATEL, Kushang V et al.American journal of human genetics. 2008, Vol 82, Num 1, pp 81-87, issn 0002-9297, 7 p.Article

Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case-Control and Prospective Cohort StudiesMALIK, Rainer; BEVAN, Steve; DE STEFANO, Anita L et al.Stroke (1970). 2014, Vol 45, Num 2, pp 394-402, issn 0039-2499, 9 p.Article

Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American CohortsBUTLER, Anne M; XIAOYAN YIN; ARKING, Dan E et al.Circulation. Cardiovascular genetics (Print). 2012, Vol 5, Num 6, pp 639-646, issn 1942-325X, 8 p.Article

Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trialsHOLMES, Michael V; NEWCOMBE, Paul; SMEETH, Liam et al.Lancet (British edition). 2011, Vol 378, Num 9791, pp 584-594, issn 0140-6736, 11 p.Article

Genome-wide Analysis of Genetic Loci Associated With Alzheimer DiseaseSESHADRI, Sudha; FITZPATRICK, Annette L; HAROLD, Denise et al.JAMA, the journal of the American Medical Association. 2010, Vol 303, Num 18, pp 1832-1840, issn 0098-7484, 9 p.Article

Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical GeneticsBIFFI, Alessandro; ANDERSON, Christopher D; DE BAKKER, Paul I. W et al.American journal of human genetics. 2010, Vol 86, Num 6, pp 904-917, issn 0002-9297, 14 p.Article

Deep sequencing of coding and non-coding RNA in the CNSVAN DER BRUG, Marcel; NALLS, Michael A; COOKSON, Mark R et al.Brain research. 2010, Vol 1338, pp 146-154, issn 0006-8993, 9 p.Article

Alterations in Muscle Attenuation following Detraining and Retraining in Resistance-Trained Older AdultsTAAFFE, Dennis R; HENWOOD, Tim R; NALLS, Michael A et al.Gerontology (Basel). 2009, Vol 55, Num 2, pp 217-223, issn 0304-324X, 7 p.Article

Reduced physical activity increases intermuscular adipose tissue in healthy young adultsMANINI, Todd M; CLARK, Brian C; NALLS, Michael A et al.The American journal of clinical nutrition. 2007, Vol 85, Num 2, pp 377-384, issn 0002-9165, 8 p.Article

Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral HemorrhageANDERSON, Christopher D; BIFFI, Alessandro; VISWANATHAN, Anand et al.Stroke (1970). 2013, Vol 44, Num 3, pp 612-619, issn 0039-2499, 8 p.Article

Common variants at 12ql4 and 12q24 are associated with hippocampal volumeBIS, Joshua C; DECARLI, Charles; SCHUUR, Maaike et al.Nature genetics. 2012, Vol 44, Num 5, pp 545-551, issn 1061-4036, 7 p.Article

Genome-Wide Association Studies of Cerebral White Matter Lesion Burden: The CHARGE ConsortiumFORNAGE, Myriam; DEBETTE, Stephanie; VROOMAN, Henri A et al.Annals of neurology. 2011, Vol 69, Num 6, pp 928-939, issn 0364-5134, 12 p.Article

Genetic Ancestry in Lung-Function PredictionsKUMAR, Rajesh; SEIBOLD, Max A; CHOUDHRY, Shweta et al.The New England journal of medicine. 2010, Vol 363, Num 4, pp 321-330, issn 0028-4793, 10 p.Article

Genome-wide association study reveals genetic risk underlying Parkinson's diseaseSIMON-SANCHEZ, Javier; SCHULTE, Claudia; KRÜGER, Rejko et al.Nature genetics. 2009, Vol 41, Num 12, pp 1308-1312, issn 1061-4036, 5 p.Article

A Genome-Wide Association Study of Depressive SymptomsHEK, Karin; DEMIRKAN, Ayse; YONGMEI LIU et al.Biological psychiatry (1969). 2013, Vol 73, Num 7, pp 667-678, issn 0006-3223, 12 p.Article

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of associationWOOD, Andrew R; HERNANDEZ, Dena G; BANDINELLI, Stefania et al.Human molecular genetics (Print). 2011, Vol 20, Num 20, pp 4082-4092, issn 0964-6906, 11 p.Article

Distinct DNA methylation changes highly correlated with chronological age in the human brainHERNANDEZ, Dena G; NALLS, Michael A; SINGLETON, Andrew B et al.Human molecular genetics (Print). 2011, Vol 20, Num 6, pp 1164-1172, issn 0964-6906, 9 p.Article

Meta-analysis of genome-wide association data identifies two loci influencing age at menarchePERRY, John R. B; STOLK, Lisette; CHERKAS, Lynn et al.Nature genetics. 2009, Vol 41, Num 6, pp 648-650, issn 1061-4036, 3 p.Article

Multiple loci influence erythrocyte phenotypes in the CHARGE ConsortiumGANESHL, Santhi K; ZAKAI, Neil A; KUHNEL, Brigitte et al.Nature genetics. 2009, Vol 41, Num 11, pp 1191-1198, issn 1061-4036, 8 p.Article

  • Page / 1