2020
article
OpenAlex
Fei Wang, Li An Lin, Jing Hu, Jianfang Zhang et autres
Sialidosis is a rare autosomal recessive hereditary disease caused by NEU1 gene mutations. A 25-year-old woman developed generalized tonic-clonic seizures since teenage, followed by progressive visional decline and limb myoclonus. Her sister had similar presentations. Both patients were products of a consanguineous …
cn
(code pays fourni par la source)
2019
book-chapter
OpenAlex
Jianchang Lin, Li An Lin, Veronica Bunn, Rachael Liu
us
(code pays fourni par la source)
Accès ouvert
2017
article
OpenAlex
Dajiang J. Liu, Gina M. Peloso, Haojie Yu, Adam S. Butterworth et autres
us, gb, pk, bd, fr, dk, it, gr, ca, fi, is, ee, se, es, cn, de, no, nl
(code pays fourni par la source)
2017
article
OpenAlex
Dajiang J. Liu, Gina M. Peloso, Haojie Yu, Adam S. Butterworth et autres
We screened variants on an exome-focused genotyping array in >300,000 participants (replication in >280,000 participants) and identified 444 independent variants in 250 loci significantly associated with total cholesterol (TC), high-density-lipoprotein cholesterol (HDL-C), low-densitylipoprotein cholesterol (LDL-C), and/or triglycerides (TG). At two loci (JAK2 …
Accès ouvert
2016
article
OpenAlex
Georg Ehret, Teresa Ferreira, Daniel I. Chasman, Ellen M. Schmidt et autres
To dissect the genetic architecture of blood pressure and assess effects on target organ damage, we analyzed 128,272 SNPs from targeted and genome-wide arrays in 201,529 individuals of European ancestry, and genotypes from an additional 140,886 individuals were used for validation. We …
Accès ouvert
2016
preprint
OpenAlex
Hieab H.H. Adams, Hadie Adams, Lenore J. Launer, Sudha Seshadri et autres
Abstract Joint analysis of data from multiple studies in collaborative efforts strengthens scientific evidence, with the gold standard approach being the pooling of individual participant data (IPD). However, sharing IPD often has legal, ethical, and logistic constraints for sensitive or high-dimensional data, …
gb, nl, us, at, fr, de, sg, is
(code pays fourni par la source)
2016
article
OpenAlex
Jianchang Lin, Li An Lin
With the recent release of FDA draft guidance (2010), adaptive designs, including adaptive randomization (e.g. response-adaptive (RA) randomization) has become popular in clinical trials because of its advantages of flexibility and efficiency gains, which also have the significant ethical advantage of assigning …
2016
article
OpenAlex
Jianchang Lin, Li An Lin
Accordingly to FDA draft guidance (2010), adaptive randomization (e.g. response-adaptive (RA) randomization) has become popular in clinical research because of its flexibility and efficiency, which also have the advantage of assigning fewer patients to inferior treatment arms. However, these designs lack a …
2015
conference-abstract
OpenAlex
Myriam Fornage, Vincent Chouraki, Li An Lin, Anita L. DeStefano et autres
White matter hyperintensities (WMH) detected on MRI are commonly identified abnormalities in the adult brain, and are associated with a greater risk of stroke, dementia, and death. Genetic factors play a significant role in WMH etiology, yet, common genetic variants identified by …
us
(code pays fourni par la source)
2015
article
OpenAlex
Li An Lin