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Showing 1–4 of 4 results

Advanced filters: Author: Ari Weinreb Clear advanced filters

Mapping a gene for combined hyperlipidaemia in a mutant mouse strain

Lawrence W. Castellani
Ari Weinreb
Aldons J. Lusis
Research01 Apr 1998
Nature Genetics

Volume: 18, P: 374-377
Population snapshots predict early haematopoietic and erythroid hierarchies

Single-cell transcriptomics, fate assays and a computational theory enable prediction of cell fates during haematopoiesis, discovery of regulators of erythropoiesis and reveal coupling between the erythroid, basophil and mast cell fates.

Betsabeh Khoramian Tusi
Samuel L. Wolock
Merav Socolovsky
Research21 Feb 2018
Nature

Volume: 555, P: 54-60
A validated disease severity scoring system for adults with type 1 Gaucher disease

Neal J Weinreb
Maria D Cappellini
Ari Zimran
Research18 Dec 2009
Genetics in Medicine

Volume: 12, P: 44-51
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

Chiea Chuen Khor, Tin Aung, Francesca Pasutto, Janey Wiggs and colleagues report a global genome-wide association study of exfoliation syndrome and a fine-mapping analysis of a previously identified disease-associated locus, LOXL1. They identify a rare protective variant in LOXL1 exclusive to the Japanese population and five new common variant susceptibility loci.

Tin Aung
Mineo Ozaki
Chiea Chuen Khor
Research29 May 2017
Nature Genetics

Volume: 49, P: 993-1004

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