Author details

Full Name

Johannah L Butler

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
26860763	Case Study: Primary Healthcare Clinical Placements during Nursing and Midwifery Education in Lesotho.	World health & population	2015
25625576	Functional significance of single nucleotide polymorphisms in the lactase gene in diverse US patients and evidence for a novel lactase persistence allele at -13909 in those of European ancestry.	J Pediatr Gastroenterol Nutr	2015
20580778	An age-dependent diet-modified effect of the PPARÎ³ Pro12Ala polymorphism in children.	Metabolism	2011
21424828	The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.	Hum Genet	2011
21423719	Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.	PLoS Genet	2011
20400458	Genome-wide association of anthropometric traits in African- and African-derived populations.	Hum Mol Genet	2010
20846217	Association of linear growth impairment in pediatric Crohn's disease and a known height locus: a pilot study.	Ann Hum Genet	2010
20839009	Association of common DNA sequence variants at 33 genetic loci with blood lipids in individuals of African ancestry from Jamaica.	Hum Genet	2010
20221249	Rapid assessment of genetic ancestry in populations of unknown origin by genome-wide genotyping of pooled samples.	PLoS Genet	2010
20430937	Fine mapping of the association with obesity at the FTO locus in African-derived populations.	Hum Mol Genet	2010
20648472	PNPLA3 variants specifically confer increased risk for histologic nonalcoholic fatty liver disease but not metabolic disease.	Hepatology	2010
19634985	Peroxisome proliferator-activated receptor-gamma (PPARgamma) Pro12Ala polymorphism and risk for pediatric obesity.	Clin Chem Lab Med	2009
19184111	Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation.	Hum Genet	2009
18728166	Association studies of common variants in 10 hypogonadotropic hypogonadism genes with age at menarche.	J Clin Endocrinol Metab	2008
18268123	Comprehensive evaluation of ESR2 variation and ovarian cancer risk.	Cancer Epidemiol Biomarkers Prev	2008
18387595	On the replication of genetic associations: timing can be everything!	Am J Hum Genet	2008
18208327	Discerning the ancestry of European Americans in genetic association studies.	PLoS Genet	2008
18391950	Identification of ten loci associated with height highlights new biological pathways in human growth.	Nat Genet	2008
17546465	Common genetic variation in eight genes of the GH/IGF1 axis does not contribute to adult height variation.	Hum Genet	2007
17465681	The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts.	PLoS Genet	2007
17057720	Transferability of tag SNPs in genetic association studies in multiple populations.	Nat Genet	2006
15546906	Determination of sequence variation and haplotype structure for the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes: investigation of role in pubertal timing.	J Clin Endocrinol Metab	2005