Haq N. Khan

Stadium Road
Karachi, SD 74800, Pakistan

Last Updated: 09/26/2026

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Found 27 publications

Spontaneous pneumomediastinum with extensive subcutaneous emphysema secondary to upper respiratory tract infection.

Spontaneous pneumomediastinum with extensive subcutaneous emphysema secondary to upper respiratory tract infection.

Journal: BMJ case reports
Published: December 26, 2025

Association of Glycoprotein GP130 Polymorphisms (rs747379809, rs754547662) with Unexplained Infertility in Women Using TETRA-ARMS-PCR.

Association of Glycoprotein GP130 Polymorphisms (rs747379809, rs754547662) with Unexplained Infertility in Women Using TETRA-ARMS-PCR.

Journal: Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
Published: June 18, 2025

Decoding rare inherited metabolic disorders: advancing precision in screening and diagnosis.

Decoding rare inherited metabolic disorders: advancing precision in screening and diagnosis.

Journal: Orphanet journal of rare diseases
Published: June 05, 2025

Unveiling clinical and genetic landscapes of MMA and CBS: insights from whole exome sequencing in a tertiary care setting.

Unveiling clinical and genetic landscapes of MMA and CBS: insights from whole exome sequencing in a tertiary care setting.

Journal: Pediatric research
Published: April 17, 2025

Exploring Proteomic Alterations in Intellectual Disability: Insights from Hyperlipidemia and Hyperphosphatasia Subgroups.

Exploring Proteomic Alterations in Intellectual Disability: Insights from Hyperlipidemia and Hyperphosphatasia Subgroups.

Journal: Neuromolecular medicine
Published: March 12, 2025

Anti-Mullerian Hormone Gene Polymorphism in Polycystic ovary syndrome: A pilot study.

Anti-Mullerian Hormone Gene Polymorphism in Polycystic ovary syndrome: A pilot study.

Journal: Pakistan journal of medical sciences
Published: March 09, 2025

Exome sequencing in a Pakistani male infertility cohort: perspective on molecular diagnosis, genetic heterogeneity, and diagnostic yield.

Exome sequencing in a Pakistani male infertility cohort: perspective on molecular diagnosis, genetic heterogeneity, and diagnostic yield.

Journal: Molecular genetics and genomics : MGG
Published: November 27, 2024

Development of low-cost in-house tetra-ARMS-PCR assay for the screening of five CBS mutations found in Pakistani homocystinuria patients.

Development of low-cost in-house tetra-ARMS-PCR assay for the screening of five CBS mutations found in Pakistani homocystinuria patients.

Journal: Nucleosides, nucleotides & nucleic acids
Published: November 16, 2023

Label free quantitative proteomic profiling of serum samples of intellectually disabled young patients revealed dysregulation of complement coagulation and cholesterol cascade systems.

Label free quantitative proteomic profiling of serum samples of intellectually disabled young patients revealed dysregulation of complement coagulation and cholesterol cascade systems.

Journal: Metabolic brain disease
Published: September 16, 2023

Genetic association of vitamin D receptor gene with female infertility.

Genetic association of vitamin D receptor gene with female infertility.

Journal: Nucleosides, nucleotides & nucleic acids
Published: July 27, 2023

Unraveling the Genetic Associations of DENND1A (rs9696009) and ERBB4 (rs2178575) with Infertile Polycystic Ovary Syndrome Females in Pakistan.

Unraveling the Genetic Associations of DENND1A (rs9696009) and ERBB4 (rs2178575) with Infertile Polycystic Ovary Syndrome Females in Pakistan.

Journal: Biochemical genetics
Published: July 20, 2023

Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Journal: Genes
Published: June 08, 2023
Showing 1-12 of 27

Last Updated: 09/26/2026