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731 results on '"Holm, Hilma"'

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201. Discovery and refinement of loci associated with lipid levels

202. The Role of Adiposity in Cardiometabolic Traits : A Mendelian Randomization Analysis

203. The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis

204. Interleukin-6 receptor pathways in coronary heart disease : a collaborative meta-analysis of 82 studies

205. Homocysteine and coronary heart disease:meta-analysis of MTHFR case-control studies, avoiding publication bias

206. Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

207. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

208. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

209. Identification of low-frequency variants associated with gout and serum uric acid levels

210. A rare variant in MYH6 is associated with high risk of sick sinus syndrome

211. RANTES/CCL5 and risk for coronary events:Results from the MONICA/KORA Augsburg case-cohort, Athero-express and CARDIoGRAM studies

212. Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

214. Aktivister. Sociala forum, globala sociala rörelser och demokratins förnyelse

215. Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism

216. Discovery of common variants associated with low TSH levels and thyroid cancer risk

217. Identification of low-frequency variants associated with gout and serum uric acid levels

218. A rare variant in MYH6 is associated with high risk of sick sinus syndrome

219. Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels

220. Correction: Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

221. Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study

222. Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

223. Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene

224. Several common variants modulate heart rate, PR interval and QRS duration

225. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

226. New common variants affecting susceptibility to basal cell carcinoma

227. Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density

228. Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

230. Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

232. Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke

233. Abstract 2921: Genome-wide Association Reveals Sequence Variants on 4q25 that Affect the Risk of Atrial Fibrillation and Stroke

234. Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the community.

235. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

236. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

237. Rare mutations associating with serum creatinine and chronic kidney disease.

238. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.

239. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

240. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

241. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.

242. Abstract 13222: Genetic Variants Close to NKX2-5and MYH6Are Associated With AV Nodal Reentry Tachycardia in First Genome-Wide Association Study

243. Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

244. Abstract 15391: Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery Disease

246. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

247. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

248. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

249. Mapping the human genetic architecture of COVID-19

250. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

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