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Journal of Medical Genetics|October 25, 2008
Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USAS Farasat, M-H Wei, M Herman, et al.
Archives of Dermatology|December 17, 2008
Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancerLaveta Stewart, Gladys M Glenn, Pamela Stratton, et al.
Placenta|May 31, 2016
Leptin reduces apoptosis triggered by high temperature in human placental villous explants: The role of the p53 pathwayAntonio Pérez-Pérez, Ayelén R Toro, Teresa Vilarino-Garcia, et al.
Human Mutation|February 26, 2009
Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis: summary of mutations (including 23 novel) and modeling of TGase-1Matthew L Herman, Sharifeh Farasat, Peter J Steinbach, et al.
Journal of Electrocardiology|August 1, 2021
Electrocardiographic findings in true acute left main coronary total occlusion a subanalisys from ATOLMA registryA Gutiérrez-Barrios, D Mialdea-Salmerón, D Cañadas-Pruaño, et al.
Cancer|April 30, 2009
Hereditary kidney cancer: unique opportunity for disease-based therapyW Marston Linehan, Peter A Pinto, Gennady Bratslavsky, et al.
American Journal of Human Genetics|October 9, 2001
Hermansky-Pudlak syndrome type 3 in Ashkenazi Jews and other non-Puerto Rican patients with hypopigmentation and platelet storage-pool deficiencyM Huizing, Y Anikster, D L Fitzpatrick, et al.
Blood|October 19, 2006
Identification of a novel chromosome region, 13q21.33-q22.2, for susceptibility genes in familial chronic lymphocytic leukemiaDavid Ng, Ousmane Toure, Ming-Hui Wei, et al.
Scientific Reports|November 23, 2016
Circulating long-non coding RNAs as biomarkers of left ventricular diastolic function and remodelling in patients with well-controlled type 2 diabetesD de Gonzalo-Calvo, F Kenneweg, C Bang, et al.
Nature Genetics|July 17, 2001
Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto RicoY Anikster, M Huizing, J White, et al.
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