Steven McGinn

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes

S. Heath, M. Farrall, H. Parving, 2008, Diabetes.

A G / T substitution in intron-1 of UNC 13 B gene is associated with increased risk of nephropathy in patients with type 1 diabetes

S. Heath, M. Farrall, D. Gauguier, 2008 .

New technologies for DNA analysis--a review of the READNA Project.

Spencer J. Gibson, H. Flyvbjerg, P. J. van der Zaag, 2016, New biotechnology.

DNA sequencing - spanning the generations.

I. Gut, S. Mcginn, Steven McGinn, 2012, New biotechnology.

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.

M. Waldenberger, H. Hakonarson, K. Strauch, 2021, European heart journal.

An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders.

S. Heath, B. Prum, M. Lathrop, 2009, The Journal of investigative dermatology.

Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress

K. Kawakami, D. Lipsker, E. Krüger, 2019, bioRxiv.

Whole‐genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140

H. Blanché, S. Saunier, A. Boland, 2018, Human mutation.