Shabir Hussain - Concepedia

Author

Shabir Hussain

Quaid-i-Azam University ORCID

Also Known As

S A Hussain, S. Hussain, Salam Abdul Wahab Hamid Abdul Hussain, Shabir Hussain, Shabir Hussain

Publications

442

Citations

H-Index

Concepts

All Affiliations

Quaid-i-Azam University Baylor Genetics Baylor College of Medicine University of Washington King Abdullah International Medical Research Center

About

Shabir Hussain is an author at Quaid-i-Azam University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	164
2	Molecular Biology	2	2	38
3	Arts	1	1	19
4	Social Sciences	1	1	12
5	Geography	1	1	12

Shabir Hussain

Publications

316

Citations

H-Index

Page 1

	Year	Citations
Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice Jae Yeon Hwang, Shoaib Nawaz, Jungmin Choi, Frontiers in Cell and Developmental Biology	2021	74
Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance Khurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza, Journal of Human Genetics Genetic DisorderGeneticsClinical SignificanceMedicineCacna1d Variants	2018	46
Biallelic variants in four genes underlying recessive osteogenesis imperfecta Amir Hayat, Shabir Hussain, Muhammad Bilal, European Journal of Medical Genetics Developmental BiologyBiallelic VariantsGenetic DisorderGeneticsOsteogenesis	2020	38
Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly Irfan Ullah, Naseebullah Kakar, Isabelle Schrauwen, Human Genetics Allelic VariantDevelopmental BiologyGenetic DisorderGeneticsMolecular Genetics	2019	23
A loss-of-function variant in DNA mismatch repair gene MLH3 underlies severe oligozoospermia Shoaib Nawaz, Muhammad Imran Ullah, Beenish Samreen Hamid, Journal of Human Genetics Genome InstabilitySomatic VariantGenetic DisorderGeneticsMolecular Biology	2021	20
A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment Isabelle Schrauwen, Imen Chakchouk, Khurram Liaqat, Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiology	2018	19
Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type Maroteaux Irfanullah Irfanullah, Amir Zeb, Naila Shinwari, The International Journal of Biochemistry & Cell Biology Silico AnalysesMendelian DisorderGenetic DisorderMedicineGenetics	2018	18
Determinants inhibiting digital payment system adoption: an Indian perspective Shabir Hussain, Sameer Gupta, Sunil Bhardwaj Qualitative Research in Financial Markets	2024	17
First evidence of involvement of TBC1D25 in causing human male infertility Shoaib Nawaz, Shabir Hussain, Sulman Basit, European Journal of Medical Genetics	2021	14
Variants in <i>GLI3</i> Cause Greig Cephalopolysyndactyly Syndrome Abdullah Abdullah, Maryam Yousaf, Zahid Azeem, Genetic Testing and Molecular Biomarkers	2019	13

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