Tooraj Mirshahi
Overview
Explore the profile of Tooraj Mirshahi including associated specialties, affiliations and a list of published articles.
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Articles
73
Citations
2407
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0
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Recent Articles
1.
Zellers M, Solanki K, Kelly M, Murphy K, Retterer K, Kirchner H, et al.
J Am Soc Nephrol
. 2024 Dec;
PMID: 39625784
No abstract available.
2.
Lona-Durazo F, Omachi K, Fermin D, Eichinger F, Troost J, Lin M, et al.
J Am Soc Nephrol
. 2024 Aug;
36(1):48-59.
PMID: 39190490
No abstract available.
3.
Kosmicki J, Marcketta A, Sharma D, Di Gioia S, Batista S, Yang X, et al.
Nat Genet
. 2024 Aug;
56(8):1592-1596.
PMID: 39103650
Coronavirus disease 2019 (COVID-19) and influenza are respiratory illnesses caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza viruses, respectively. Both diseases share symptoms and clinical risk...
4.
Xu H, Gupta S, Dinsmore I, Kollu A, Cawley A, Anwar M, et al.
medRxiv
. 2024 Jun;
PMID: 38903089
Genome-wide association studies (GWAS) have identified numerous body mass index (BMI) loci. However, most underlying mechanisms from risk locus to BMI remain unknown. Leveraging omics data through integrative analyses could...
5.
Zellers M, Solanki K, Kelly M, Murphy K, Retterer K, Kirchner H, et al.
medRxiv
. 2024 Jun;
PMID: 38883771
Introduction: Our knowledge of X-linked Alport Syndrome [AS] comes mostly from selected cohorts with more severe disease. Methods: We examined the phenotypic spectrum of X-linked AS in males and females...
6.
Ghouse J, Sveinbjornsson G, Vujkovic M, Seidelin A, Gellert-Kristensen H, Ahlberg G, et al.
Nat Genet
. 2024 Apr;
56(5):827-837.
PMID: 38632349
We report a multi-ancestry genome-wide association study on liver cirrhosis and its associated endophenotypes, alanine aminotransferase (ALT) and γ-glutamyl transferase. Using data from 12 cohorts, including 18,265 cases with cirrhosis,...
7.
Gagliano Taliun S, Dinsmore I, Mirshahi T, Chang A, Paterson A, Barua M
Sci Rep
. 2024 Jan;
14(1):1125.
PMID: 38212389
No abstract available.
8.
Gagliano Taliun S, Dinsmore I, Mirshahi T, Chang A, Paterson A, Barua M
Sci Rep
. 2023 Oct;
13(1):18084.
PMID: 37872228
Our GWAS of hematuria in the UK Biobank identified 6 loci, some of which overlap with loci for albuminuria suggesting pleiotropy. Since clinical syndromes are often defined by combinations of...
9.
Solanki K, Hu Y, Moore B, Abedi V, Avula V, Mirshahi T, et al.
Kidney Int Rep
. 2023 Oct;
8(10):2088-2099.
PMID: 37849993
Introduction: The penetrance and phenotypic spectrum of autosomal dominant Alport Syndrome (ADAS), affecting 1 in 106, remains understudied. Methods: Using data from 174,418 participants in the Geisinger MyCode/DiscovEHR study, an...
10.
Immadisetty K, Fang X, Ramon G, Hartle C, McCoy T, Center R, et al.
J Mol Cell Cardiol
. 2023 May;
180:69-83.
PMID: 37187232
Congenital long QT syndrome (LQTS) is characterized by a prolonged QT-interval on an electrocardiogram (ECG). An abnormal prolongation in the QT-interval increases the risk for fatal arrhythmias. Genetic variants in...