S. Daud

发表

Detection of BRCA1/2 mutations in breast cancer patients from Thailand and Pakistan

S. Sangrajrang, V. Gaborieau, O. Sinilnikova, 2012, Clinical genetics.

Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia

G. Nürnberg, P. Nürnberg, C. Kubisch, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

In‐Silico Analysis of Gene ALS2 Genetic Variants Identified in the Affected Horses and Humans With Motor Neuron Disease

T. Yaqub, S. Umar, M. Wasim, 2018 .

Genetic data of 22 autosomal STR loci in Khyber-Pakhtunkhwa, Balochistan and Gilgit Baltistan population of Pakistan using PowerPlex® fusion system.

Muhammad Shafique, M. Shahzad, Ahmad Ali Shahid, 2022, Legal medicine.

An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group

J. Oldenburg, G. Nürnberg, P. Nürnberg, 2012, Human Genetics.

Microbial pollution in inland recreational freshwaters of Quetta, Pakistan: an initial report.

M. Luqman, A. Yousafzai, S. Daud, 2022, Journal of water and health.

Mutational spectrum of the TYR and SLC45A2 genes in Pakistani families with oculocutaneous albinism, and potential founder effect of missense substitution (p.Arg77Gln) of tyrosinase

J. Ahmad, M. Babar, A. H. Baloch, 2015, Clinical and experimental dermatology.

Identification of a novel mutation (p.Ile198Thr) in gene TYR in a Pakistani family with nonsyndromic oculocutaneous albinism

J. Ahmad, M. Babar, S. Daud, 2014, Clinical and experimental dermatology.

Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family

Abdul Hadi Almazroea, M. Ayub, Rozeena Shaikh, 2023, Medicina.

Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts

H. Bolz, G. Nürnberg, P. Nürnberg, 2011, Molecular vision.

A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly.

G. Nürnberg, P. Nürnberg, C. Kubisch, 2012, European journal of medical genetics.

Risk factors for lung cancer in the Pakistani population.

Amin U. Khan, M. Javed, Muhammad Luqman, 2014, Asian Pacific journal of cancer prevention : APJCP.

A missense mutation (p.G274R) in gene ASPA causes Canavan disease in a Pakistani family

J. Ahmad, R. Hussain, M. A. Kakar, 2012, Molecular Biology Reports.

Current Trends in OMICS

Nisar, J. Ahmad, M. Luqman, 2022 .

Metaplastic Carcinoma of the Breast: A Clinical Study of 7 Cases from Balochistan

J. Ahmad, A. M. Cheema, A. H. Baloch, 2014 .

Optimization and Validation of PCR protocol for three Hypervariable Regions (HVI, HVII and HVIII) in Human Mitochondrial DNA

A. Naeem, T. Husnain, Muhammad Shafique, 2014 .

An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group

J. Oldenburg, G. Nürnberg, P. Nürnberg, 2011, Human Genetics.

Missense mutations (p.H371Y, p.D438Y) in gene CHEK2 are associated with breast cancer risk in women of Balochistan origin

A. Rehman, J. Ahmad, Akhtar Ali, 2014, Molecular Biology Reports.

Various aspects, patterns and risk factors in breast cancer patients of Balochistan.

J. Ahmad, Muneer Ahmed, M. A. Kakar, 2012, Asian Pacific journal of cancer prevention : APJCP.

A Missense Pathogenic Variant in a Conserved Region of CNTNAP2 Is Associated with Obesity, Seizures, and Language Impairment in a Pakistani Family

M. T. Pervez, A. H. Baloch, S. Daud, 2023, Molecular Syndromology.