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Author Details

Gabriela L Surdulescu
2004
41
26
PMIDPaper TitleJournal TitlePublished Year
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
26014426Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes.Eur J Hum Genet2016
26911590Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.BMC Genomics2016
27398621The genetic architecture of type 2 diabetes.Nature2016
26762129Quantitative genetics of circulating Dickkopf-related protein 1 (DKK1) in community-based sample of UK twins.Osteoporos Int2016
25989729Erratum: Whole-genome sequence-based analysis of thyroid function.Nat Commun2015
25743335Whole-genome sequence-based analysis of thyroid function.Nat Commun2015
25625282Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.PLoS Genet2015
24586183Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.PLoS Genet2014
24493200Assessment of age-related changes in heritability and IGF-1 gene effect on circulating IGF-1 levels.Age (Dordr)2014
23381943Ischemic stroke is associated with the ABO locus: the EuroCLOT study.Ann Neurol2013
22945461Genome-wide association study reveals a complex genetic architecture underpinning-induced CYP3A4 enzyme activity.European Journal of Drug Metabolism and Pharmacokinetics2013
23477808Elevated plasma fractalkine levels are associated with higher levels of IL-6, Apo-B, LDL-C and insulin, but not with body composition in a large female twin sample.Metabolism2013
23261412Contribution of putative genetic factors and candidate gene variants to inter-individual variation of circulating fractalkine (CX3CL1) levels in a large UK twins' sample.Hum Immunol2013
23284290Genes contributing to pain sensitivity in the normal population: an exome sequencing study.PLoS Genet2012
22884971Copy number variation of the APC gene is associated with regulation of bone mineral density.Bone2012
22941192Mapping cis- and trans-regulatory effects across multiple tissues in twins.Nat Genet2012
21789213The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits.PLoS One2011
21304890The architecture of gene regulatory variation across multiple human tissues: the MuTHER study.PLoS Genet2011
21625172The basis of differential responses to folic acid supplementation.Journal of Nutrigenetics and Nutrigenomics2011
21750469Genetic epidemiology of induced CYP3A4 activity.Pharmacogenetics and Genomics2011
20826269A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study.Am J Hum Genet2010
19150881Identification of quantitative trait loci for fibrin clot phenotypes: the EuroCLOT study.Arterioscler Thromb Vasc Biol2009
19453265Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro.J Bone Miner Res2009
19209234Epidemiology and genetic epidemiology of the liver function test proteins.PLoS One2009
18227361The association between physical activity in leisure time and leukocyte telomere length.Arch Intern Med2008
17970774Heritability of serum TSH, free T4 and free T3 concentrations: a study of a large UK twin cohort.Clin Endocrinol (Oxf)2008
18611976Genetic loci linked to pituitary-thyroid axis set points: a genome-wide scan of a large twin cohort.J Clin Endocrinol Metab2008
18624800Migraine and antiphospholipid antibodies: no association found in migraine-discordant monozygotic twins.Cephalalgia2008
17195216Sex and ethnic differences in the association of ASPN, CALM1, COL2A1, COMP, and FRZB with genetic susceptibility to osteoarthritis of the knee.Arthritis Rheum2007
17712044The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans.Blood2007
17991655Higher serum vitamin D concentrations are associated with longer leukocyte telomere length in women.Am J Clin Nutr2007
16391564Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.Eur J Hum Genet2006
16400618Mapping genetic loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs.Am J Hum Genet2006
16856882The effects of social status on biological aging as measured by white-blood-cell telomere length.Aging Cell2006
16453284Reproducible genetic associations between candidate genes and clinical knee osteoarthritis in men and women.Arthritis Rheum2006
16861354cMYB is involved in the regulation of fetal hemoglobin production in adults.Blood2006
16135557Identification of QTLs for serum lipid levels in a female sib-pair cohort: a novel application to improve the power of two-locus linkage analysis.Hum Mol Genet2005
15334463Association study of candidate genes for the prevalence and progression of knee osteoarthritis.Arthritis Rheum2004
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