Hafiz Baig

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Title(s)	Postdoctoral Scholar, Ophthalmology
School	Vc-health Sciences-schools
Address	9500 Gilman Drive # La Jolla CA 92093
vCard	Download vCard

Bibliographic

selected publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

Altmetrics Details

PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.

A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort. NPJ Genom Med. 2025 Apr 04; 10(1):31. Ullah M, Rehman AU, Quinodoz M, Rashid A, Cancellieri F, Munir A, Kaminska K, Iqbal A, Javed S, Dawood M, Baig HMA, Saleha S, Naz S, Kausar H, Waryah AM, Superti-Furga A, Ansar M, Rivolta C. PMID: 40180963; PMCID: PMC11968986.

View in: PubMed Mentions: 2
Optimized Prime Editing of Human Induced Pluripotent Stem Cells to Efficiently Generate Isogenic Models of Mendelian Diseases. Int J Mol Sci. 2024 Dec 26; 26(1). Cerna-Chavez R, Ortega-Gasco A, Baig HMA, Ehrenreich N, Metais T, Scandura MJ, Bujakowska K, Pierce EA, Garita-Hernandez M. PMID: 39795970; PMCID: PMC11719581.

View in: PubMed Mentions: Fields:
Bio Biochemistry Che Chemistry Mol Molecular Biology
Translation:Humans Cells
Association of Lower Rostral Anterior Cingulate GABA+ and Dysregulated Cortisol Stress Response With Altered Functional Connectivity in Young Adults With Lifetime Depression: A Multimodal Imaging Investigation of Trait and State Effects. Am J Psychiatry. 2024 Jul 01; 181(7):639-650. Ironside M, Duda JM, Moser AD, Holsen LM, Zuo CS, Du F, Perlo S, Richards CE, Chen X, Nickerson LD, Null KE, Esfand SM, Alexander MM, Crowley DJ, Lauze M, Misra M, Goldstein JM, Pizzagalli DA. PMID: 38685857; PMCID: PMC11216878.

View in: PubMed Mentions: 3 Fields:
Psy Psychiatry
Translation:Humans
Porcine reproductive and respiratory syndrome virus degrades DDX10 via SQSTM1/p62-dependent selective autophagy to antagonize its antiviral activity. Autophagy. 2023 08; 19(8):2257-2274. Li J, Zhou Y, Zhao W, Liu J, Ullah R, Fang P, Fang L, Xiao S. PMID: 36779599; PMCID: PMC10351467.

View in: PubMed Mentions: 23 Fields:
Cel Cell Biology
Translation:Animals Cells
Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees. Genes (Basel). 2023 02 03; 14(2). Rao AR, Nazir A, Imtiaz S, Paracha SA, Waryah YM, Ujjan ID, Anwar I, Iqbal A, Santoni FA, Shah I, Gul K, Baig HMA, Waryah AM, Antonarakis SE, Ansar M. PMID: 36833331; PMCID: PMC9956862.

View in: PubMed Mentions: 7 Fields:
Gen Genetics
Translation:Humans
[Determination of organophosphate diesters in facility vegetable soils using ultra-high performance liquid chromatography-electrostatic field orbitrap high resolution mass spectrometry]. Se Pu. 2023 Jan; 41(1):58-65. Liu M, Wang M, Zhao A, Zhu L, Wang C, Wei C, Liu W, Xu J. PMID: 36633077; PMCID: PMC9837671.

View in: PubMed Mentions: Fields:
Che Chemistry Techniques
Translation:Humans Animals
A new nonsense mutation in HMX1 in two siblings with oculoauricular syndrome. Ophthalmic Genet. 2022 10; 43(5):720-723. Ansar M, Javed S, Baig HMA, Quinodoz M, Ullah M, Han JH, Rahim MU, Kausar H, Calzetti G, Rivolta C. PMID: 35946463.

View in: PubMed Mentions: 1 Fields:
Gen Genetics Oph Ophthalmology
Translation:Humans
Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder. NPJ Genom Med. 2021 Nov 11; 6(1):94. Mattioli F, Darvish H, Paracha SA, Tafakhori A, Firouzabadi SG, Chapi M, Baig HMA, Reymond A, Antonarakis SE, Ansar M. PMID: 34764295; PMCID: PMC8586153.

View in: PubMed Mentions: 20
Whole exome sequencing revealed novel variants in consanguineous Pakistani families with intellectual disability. Genes Genomics. 2021 05; 43(5):503-512. Rasool IG, Zahoor MY, Iqbal M, Anjum AA, Ashraf F, Abbas HQ, Baig HMA, Mahmood T, Shehzad W. PMID: 33710595.

View in: PubMed Mentions: 5 Fields:
Gen Genetics
Translation:Humans
Injury, Illness, and Mental Health Risks in United States Domestic Mariners. J Occup Environ Med. 2020 10; 62(10):839-841. Lefkowitz RY, Null DB, Slade MD, Redlich CA. PMID: 32769797.

View in: PubMed Mentions: 6 Fields:
Env Environmental Health Occ Occupational Medicine
Translation:Humans
Imaging examination, diagnosis, and control and prevention of nosocomial infection for coronavirus disease 2019: Expert consensus of Hunan radiologist. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020 Mar 28; 45(3):221-228. Liu J, Wang W. PMID: 32386011.

View in: PubMed Mentions: 2 Fields:
Med Medicine (General)
Translation:Humans Cells PHPublic Health