About: Carl D. Langefeld

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Ph.D. University of Michigan 1999

Attributes	Values
rdf:type	Item
description	Ph.D. University of Michigan 1999 (en)
rdfs:label	Carl D. Langefeld (en) Carl D. Langefeld (ga) Carl Duane Langefeld (nl)
skos:prefLabel	Carl D. Langefeld (en) Carl D. Langefeld (ga) Carl Duane Langefeld (nl)
name	Carl D. Langefeld (en) Carl D. Langefeld (ga) Carl Duane Langefeld (nl)
LinkedIn personal profile ID	wds:Q102208371-2904310e-4da8-a933-6838-7182865327b0
LinkedIn personal profile ID	carl-langefeld-73007b7
given name	wds:Q102208371-2FE9CFC9-11CA-481C-BAC7-7425B4B118B6 wds:Q102208371-2a7e7340-480c-2dea-4d56-d6e655408572
given name	Carl Duane
instance of	wds:Q102208371-E61F9DAA-7495-4CF4-957E-BFDE009BC7FA
instance of	Homo sapiens
doctoral advisor	wds:Q102208371-c9e97b56-9057-412c-b4ec-5eabbafe62f2
Google Knowledge Graph ID	wds:Q102208371-51d67d19-46dc-cc25-d289-ed6675d7afbb
MR Author ID	wds:Q102208371-4E54D296-2E84-4003-9611-B4E657D1B063
Mathematics Genealogy Project ID	wds:Q102208371-2A03E7C6-516B-4AE1-8091-938037E13503
Google Knowledge Graph ID	http://g.co/kg/g/11d_8stfbl
doctoral advisor	Michael Boehnke
Google Knowledge Graph ID	/g/11d_8stfbl
MR Author ID	1048745
Mathematics Genealogy Project ID	47716
ResearchGate profile ID	wds:Q102208371-F10403B9-CDA1-46B7-B0B1-E9C840CCBA57
ResearchGate profile ID	Carl-Langefeld
skos:altLabel	Carl D Langefeld (en) Carl D Langefeld (nl) Carl Duane Langefeld (en)
occupation	wds:Q102208371-af9b29f7-46a2-5443-1db0-a5812ecf263a
employer	wds:Q102208371-fd589506-479f-20fc-7ee1-91b37311b966
sex or gender	wds:Q102208371-3E88EC3C-4B4D-4254-ADD8-8481C9254A39
educated at	wds:Q102208371-e0dffbf1-2425-4552-b774-06841d74162b
family name	wds:Q102208371-b0edf96c-4474-524f-9913-a9ecadda80a7
WorldCat Identities ID (superseded)	wds:Q102208371-e510aaef-49ba-e71d-ecd5-4eab548d08d3
occupation	biostatistician
employer	Wake Forest School of Medicine
sex or gender	male
educated at	University of Michigan
family name	Langefeld
WorldCat Identities ID (superseded)	np-langefeld, carl d
is owl:sameAs of	Carl D. Langefeld
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q102208371
is author of	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Polymorphisms near SOCS3 are associated with obesity and glucose homeostasis traits in Hispanic Americans from the Insulin Resistance Atherosclerosis Family Study Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study. Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans Association of adiponectin gene polymorphisms with type 2 diabetes in an African American population enriched for nephropathy Heritability of GFR and albuminuria in Caucasians with type 2 diabetes mellitus Bone morphogenetic protein 7 (BMP7) gene polymorphisms are associated with inverse relationships between vascular calcification and BMD: the Diabetes Heart Study Apolipoprotein E, statins, and risk of intracerebral hemorrhage Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study Genetic ancestry, serum interferon-α activity, and autoantibodies in systemic lupus erythematosus Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups The APOL1 gene and allograft survival after kidney transplantation The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13 Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage Apolipoprotein L1 gene variants in deceased organ donors are associated with renal allograft failure Association of the estrogen receptor-alpha gene with the metabolic syndrome and its component traits in African-American families: the Insulin Resistance Atherosclerosis Family Study. Investigation of the estrogen receptor-alpha gene with type 2 diabetes and/or nephropathy in African-American and European-American populations Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry Genome-wide association of BMI in African Americans Implication of European-derived adiposity loci in African Americans Analysis of FTO gene variants with measures of obesity and glucose homeostasis in the IRAS Family Study Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma A genome scan for fasting insulin and fasting glucose identifies a quantitative trait locus on chromosome 17p: the insulin resistance atherosclerosis study (IRAS) family study. Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing Interferon regulatory factor-5 is genetically associated with systemic lupus erythematosus in African Americans Informed conditioning on clinical covariates increases power in case-control association studies Ordered subset analysis in genetic linkage mapping of complex traits The role of genetic variation near interferon-kappa in systemic lupus erythematosus Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus ABIN1 dysfunction as a genetic basis for lupus nephritis Identification of IRAK1 as a risk gene with critical role in the pathogenesis of systemic lupus erythematosus Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans Association of trypanolytic ApoL1 variants with kidney disease in African Americans A genome-wide association study for diabetic nephropathy genes in African Americans Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15. Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans

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