Author

Roohia Khanam

Institution: Forman Christian College

Observed institution: Forman Christian College

ORCID: 0000-0001-6826-7471

Observed ORCID: 0000-0001-6826-7471

OpenAlex ID: A5012839773

High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor

2023 · Sadia Saeed, Roohia Khanam, et al. · Cell Reports Medicine · 38

Rare Variant Analysis of Obesity-Associated Genes in Young Adults With Severe Obesity From a Consanguineous Population of Pakistan

2022 · Sadia Saeed, Qasim M. Janjua, et al. · Diabetes · 22

Biallelic Mutations in P4HTM Cause Syndromic Obesity

2023 · Sadia Saeed, Lijiao Ning, et al. · Diabetes · 17

Biallelic variants in SREK1 downregulating SNORD115 and SNORD116 cause a Prader-Willi–like syndrome

2025 · Sadia Saeed, Anna-Maria Siegert, et al. · Journal of Clinical Investigation · 3

Biallelic mutations in P4HTM cause syndromic obesity

2023 · Sadia Saeed, Lijiao Ning, et al. · 2

Inversed impaired osteogenic activity in children with severe obesity due to MC4R deficiency compared to LEP and LEPR deficiency

2026 · Qasim M. Janjua, Roohia Khanam, et al. · International Journal of Obesity

Biallelic mutations in P4HTM cause syndromic obesity

2023 · Sadia Saeed, Lijiao Ning, et al.

Rare Variant Analysis of Obesity-Associated Genes in Young Adults With Severe Obesity From a Consanguineous Population of Pakistan

2022 · Sadia Saeed, Qasim M Janjua, et al.

Works count: 9

Citation count: 82

H-index: 3

I10-index: 3