J. Wasson

发表

Genetic epidemiology of diabetes.

M. Permutt, N. Cox, Nancy Cox, 2005, The Journal of clinical investigation.

An E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene (Kir6.2) contributes as much to the risk of Type II diabetes in Caucasians as the PPARγ Pro12Ala variant

M. Permutt, B. Suarez, J. Lin, 2002, Diabetologia.

A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population.

S. Lewitzky, M. Permutt, B. Suarez, 2001, Diabetes.

Characterization of the LIM/Homeodomain Gene Islet-1 and Single Nucleotide Screening in NIDDM

M. Permutt, P. Froguel, M. Vaxillaire, 1995, Diabetes.

Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes

M. Permutt, B. Glaser, J. Wasson, 2001, Diabetologia.

An Asian Indian woman with Wolfram syndrome on insulin pump: successful pregnancy and beyond.

M. Permutt, J. Kesavadev, A. Shankar, 2011, Diabetes technology & therapeutics.

Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis

M. Permutt, R. Schmidt, M. Ohsugi, 2005, Diabetologia.

Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.

P. Behn, M. Permutt, B. Glaser, 1998, Diabetes.

Neuroblastoma: Effect of genetic factors on prognosis and treatment

A. Nakagawara, R. Seeger, G. Brodeur, 1992, Cancer.

Oncogene amplification in pediatric brain tumors.

A. Look, D. Bigner, P. Burger, 1990, Cancer research.

Mapping Novel Pancreatic Islet Genes to Human Chromosomes

M. Permutt, M. Mueckler, H. Donis-Keller, 1997, Diabetes.

Mapping of the human insulin receptor substrate-2 gene, identification of a linked polymorphic marker and linkage analysis in families with Type II diabetes: no evidence for a major susceptibility role

M. Permutt, B. Glaser, K. Kalidas, 1998, Diabetologia.

Molecular Analysis of Gene Amplification in Tumors

G. Brodeur, J. Wasson, Jonathon C. Wasson, 1994, Current protocols in human genetics.

A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

Benjamin Glaser, M. Permutt, B. Suarez, 2004, Diabetes.

Neuroimaging evidence of deficient axon myelination in Wolfram syndrome

L. Tychsen, J. Shimony, F. Urano, 2016, Scientific Reports.

Phenotypic characteristics of early Wolfram syndrome

M. Permutt, J. Shimony, T. Hershey, 2013, Orphanet Journal of Rare Diseases.

Allele quantification and DNA pooling methods.

J. Wasson, 2007, Methods in molecular biology.

Diabetes mellitus and optic atrophy: a study of Wolfram syndrome in the Lebanese population.

J. Loiselet, S. Azar, A. Permutt, 2004, The Journal of clinical endocrinology and metabolism.

Candidate gene studies reveal that the WFS1 gene joins the expanding list of novel type 2 diabetes genes

M. Permutt, J. Wasson, 2008, Diabetologia.

Cloning of human pancreatic islet large conductance Ca2+-activated K+ channel (hSlo) cDNAs: evidence for high levels of expression in pancreatic islets and identification of a flanking genetic marker

M. Permutt, L. Salkoff, J. Ferrer, 1996, Diabetologia.

Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation

T. Hansen, O. Pedersen, T. Jørgensen, 2008, Diabetologia.

Isolation and characterization of the human PAX4 gene.

P. Behn, M. Permutt, B. Glaser, 1998, Diabetes.