关注
Ihsan Ullah
Ihsan Ullah
Boston children hospital, Harvard Medical School
在 uvas.edu.pk 的电子邮件经过验证
标题
引用次数
引用次数
年份
Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis
A Amar, AJ Majmundar, I Ullah, A Afzal, DA Braun, S Shril, A Daga, ...
Human genetics 138, 211-219, 2019
412019
Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice
AJ Majmundar, F Buerger, TA Forbes, V Klämbt, R Schneider, K Deutsch, ...
Science advances 7 (1), eabe1386, 2021
312021
Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutation
S Ijaz, MY Zahoor, M Imran, S Afzal, MA Bhinder, I Ullah, HA Cheema, ...
Journal of Pediatric Endocrinology and Metabolism 29 (3), 327-332, 2016
132016
An in vitro antiviral activity of iodine complexes against SARS-CoV-2
I Altaf, MF Nadeem, N Hussain, M Nawaz, S Raza, MA Shabbir, ...
Archives of Microbiology 203 (7), 4743-4749, 2021
92021
Association study of CLDN14 variations in patients with kidney stones
I Ullah, K Murtaza, H Ammara, Misbah, MA Bhinder, A Riaz, W Shehzad, ...
Open Life Sciences 17 (1), 81-90, 2022
62022
Vitamin E boosted the protective potential of Aloe vera in CCl4-treated rats
R Fatima, MS Yasin, H Anwar, I Ullah, W Shehzad, I Murtaza, T Ali
Biologia, 1-8, 2021
52021
Mitochondrial DNA diversity and maternal origins of Pakistani donkey
S Earnist, S Nawaz, I Ullah, MA Bhinder, M Imran, MA Rasheed, ...
Brazilian Journal of Biology 84, e256942, 2022
32022
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis
AJ Majmundar, E Widmeier, JF Heneghan, A Daga, CHW Wu, F Buerger, ...
Genetics in Medicine 25 (3), 100351, 2023
12023
Sequencing the CaSR locus in Pakistani stone formers reveals a novel loss-of-function variant atypically associated with nephrolithiasis
I Ullah, I Ottlewski, W Shehzad, A Riaz, S Ijaz, A Tufail, H Ammara, ...
BMC Medical Genomics 14, 1-7, 2021
12021
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