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The Kalash Genetic Isolate: Ancient divergence, drift and selection

American journal of human genetics, 2015-05, Vol.96 (5), p.775-783

2015

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"Like sugar in milk": reconstructing the genetic history of the Parsi population

Genome Biology, 2017-06, Vol.18 (1), p.110-110, Article 110

2017

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Refined Geographic Distribution of the Oriental ALDH2504Lys (nee 487Lys) Variant

Annals of human genetics, 2009-05, Vol.73 (3), p.335-345

2009

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Response to Hellenthal et al

American journal of human genetics, 2016-02, Vol.98 (2), p.398-398

2016

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A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan

Gene, 2012-07, Vol.502 (2), p.133-137

2012

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Analysis of the glutathione S-transferase genes polymorphisms in the risk and prognosis of renal cell carcinomas. Case-control and meta-analysis

Urologic oncology, 2016-09, Vol.34 (9), p.419.e1-419.e12

2016

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The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans

American journal of human genetics, 2010-02, Vol.86 (2), p.161-171

2010

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Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children

Gene, 2012-02, Vol.493 (1), p.165-168

2012

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Locus heterogeneity in autosomal recessive congenital cataracts : linkage to 9q and germline HSF4 mutations

Human genetics, 2005-09, Vol.117 (5), p.452-459

2005

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The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection

Inflammation research, 2017-05, Vol.66 (5), p.425-432

2017

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Monoamine Oxidase A gene polymorphisms and self reported aggressive behaviour in a Pakistani ethnic group

Journal of the Pakistan Medical Association, 2015-08, Vol.65 (8), p.818-824

2015

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The effect of chemokine receptor gene polymorphisms (CCR2V64I, CCR5-59029G>A and CCR5Δ32) on renal allograft survival in Pakistani transplant patients

Gene, 2012-12, Vol.511 (2), p.314-319

2012

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HLA class I and II polymorphisms in the Gujjar population from Pakistan

Immunological investigations, 2013-01, Vol.42 (8), p.691-700

2013

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Erratum to “Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children” [Gene 493 (2012) 165–168]

Gene, 2012-03, Vol.495 (1), p.93-93

2012

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Association of a single-nucleotide polymorphism in the promoter region of the VEGF gene with the risk of renal cell carcinoma

Genetic testing and molecular biomarkers, 2011-09, Vol.15 (9), p.653-657

2011

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Polymorphisms in the methylene tetrahydrofolate reductase gene and their unique combinations are associated with an increased susceptibility to the renal cancers

Genetic testing and molecular biomarkers, 2012-05, Vol.16 (5), p.346-352

2012

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Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2

American journal of medical genetics. Part A, 2007-12, Vol.143A (23), p.2768-2774

2007

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The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans

American journal of human genetics, 2010, Vol.86 (2), p.161-171

2010

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Mapping of a Novel Type III Variant of Knobloch Syndrome (KN03) to Chromosome 17qll.2

American journal of medical genetics. Part A, 2007, Vol.143 (23), p.2768-2774

2007

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Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan

Mutation research, 2014-05, Vol.763-764, p.45-52

2014

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Human leukocyte antigen (HLA) class II association with rheumatic heart disease in Pakistan

The Journal of heart valve disease, 2007-05, Vol.16 (3), p.300

2007

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A Survey on Clustering Algorithms in Wireless Sensor Networks: Challenges, Research, and Trends

2020 International Computer Symposium (ICS), 2020, p.294-299

2020

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The Kalash Genetic Isolate: Ancient divergence, drift and selection

"Like sugar in milk": reconstructing the genetic history of the Parsi population

Refined Geographic Distribution of the Oriental ALDH2504Lys (nee 487Lys) Variant

Response to Hellenthal et al

A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan

Analysis of the glutathione S-transferase genes polymorphisms in the risk and prognosis of renal cell carcinomas. Case-control and meta-analysis

The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans

Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children

Locus heterogeneity in autosomal recessive congenital cataracts : linkage to 9q and germline HSF4 mutations

The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection

Monoamine Oxidase A gene polymorphisms and self reported aggressive behaviour in a Pakistani ethnic group

The effect of chemokine receptor gene polymorphisms (CCR2V64I, CCR5-59029G>A and CCR5Δ32) on renal allograft survival in Pakistani transplant patients

HLA class I and II polymorphisms in the Gujjar population from Pakistan

Erratum to “Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children” [Gene 493 (2012) 165–168]

Association of a single-nucleotide polymorphism in the promoter region of the VEGF gene with the risk of renal cell carcinoma

Polymorphisms in the methylene tetrahydrofolate reductase gene and their unique combinations are associated with an increased susceptibility to the renal cancers

Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2

The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans

Mapping of a Novel Type III Variant of Knobloch Syndrome (KN03) to Chromosome 17qll.2

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan

Human leukocyte antigen (HLA) class II association with rheumatic heart disease in Pakistan

A Survey on Clustering Algorithms in Wireless Sensor Networks: Challenges, Research, and Trends

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