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Shakeela Daud
Observed names:
Daud, Shakeela,
S Daud,
S. Daud,
S., Daud,
Shakeela daud
Institution:
Balochistan University of Information Technology, Engineering and Management Sciences
Observed institutions:
Balochistan University of Information Technology, Engineering and Management Sciences,
University of the Punjab,
Centre of Excellence in Molecular Biology,
University of Veterinary and Animal Sciences
ORCID:
0000-0002-4886-4751
Observed ORCID:
0000-0002-4886-4751
OpenAlex ID:
A5044078741
Risk Factors for Lung Cancer in the Pakistani Population
2014
·
Muhammad Luqman
, Muhammad Mohsin Javed
, et al.
·
Asian Pacific Journal of Cancer Prevention
·
77
PDF
A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly
2012
·
Naseebullah Kakar
, Ingrid Goebel
, et al.
·
European Journal of Medical Genetics
·
46
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group
2011
·
Guntram Borck
, Naseebullah Kakar
, et al.
·
Human Genetics
·
21
Missense mutations (p.H371Y, p.D438Y) in gene CHEK2 are associated with breast cancer risk in women of Balochistan origin
2014
·
Abdul Hameed Baloch
, Shakeela Daud
, et al.
·
Molecular Biology Reports
·
17
Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts.
2011
·
Adeel Ahmad
, Shakeela Daud
, et al.
·
PubMed
·
17
Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia
2016
·
Shakeela Daud
, Naseebullah Kakar
, et al.
·
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
·
16
Mutational spectrum of theTYRandSLC45A2genes in Pakistani families with oculocutaneous albinism, and potential founder effect of missense substitution (p.Arg77Gln) of tyrosinase
2015
·
S. A. Shah
, N. Raheem
, et al.
·
Clinical and Experimental Dermatology
·
15
Various Aspects, Patterns and Risk Factors in Breast Cancer Patients of Balochistan
2012
·
Abdul Hameed Baloch
, Jameela Shuja
, et al.
·
Asian Pacific Journal of Cancer Prevention
·
15
PDF
Y-chromosomal STR analysis in the Pashtun population of Southern Afghanistan
2011
·
Niaz M. Achakzai
, Z. Rahman
, et al.
·
Forensic Science International Genetics
·
15
Detection of BRCA1/2 mutations in breast cancer patients from Thailand and Pakistan
2012
·
J Ahmad
, F Le Calvez‐Kelm
, et al.
·
Clinical Genetics
·
9
Microbial pollution in inland recreational freshwaters of Quetta, Pakistan: an initial report
2022
·
Muhammad Luqman
, Muhammad Umer Farooq Awan
, et al.
·
Journal of Water and Health
·
7
Identification of a novel mutation (p.Ile198Thr) in geneTYRin a Pakistani family with nonsyndromic oculocutaneous albinism
2014
·
S. A. Shah
, S. U. Din
, et al.
·
Clinical and Experimental Dermatology
·
7
A missense mutation (p.G274R) in gene ASPA causes Canavan disease in a Pakistani family
2012
·
Rashida Hussain
, Shakeela Daud
, et al.
·
Molecular Biology Reports
·
7
Optimization and Validation of PCR protocol for three Hypervariable Regions (HVI, HVII and HVIII) in Human Mitochondrial DNA
2014
·
Shakeela Daud
, Saqib Shahzad
, et al.
·
Advancements in Life Sciences (University of the Punjab)
·
5
A Missense Pathogenic Variant in a Conserved Region of CNTNAP2 Is Associated with Obesity, Seizures, and Language Impairment in a Pakistani Family
2023
·
Sara Naudhani
, Adeel Ahmad
, et al.
·
Molecular Syndromology
·
4
PDF
Genetic data of 22 autosomal STR loci in Khyber-Pakhtunkhwa, Balochistan and Gilgit Baltistan population of Pakistan using PowerPlex® fusion system
2022
·
Muhammad Shafique
, Namra Sajid
, et al.
·
Legal Medicine
·
3
Targeted Sequencing of HEXA Gene Shows Missense Substitution (p.Arg499His) in a Large Pakistani Family with Tay-Sachs Disease
2024
·
Fariya Khan Bazai
, Mehmood Ul Hassan
, et al.
·
Cytology and Genetics
·
2
Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family
2023
·
Abdulhadi Almazroea
, Ambreen Ijaz
, et al.
·
Medicina
·
2
PDF
Identification of Mutations in Gene BRCA1/2 in Breast Cancer Cases from Balochistan, Pakistan
2019
·
Asma Yousafzai
, Muhammad Luqman
, et al.
·
Pakistan Journal of Zoology
·
2
Exonic Deletion in MAN1B1 and a Missense Substitution in CAPN10 Causes Truncal Obesity, Type 2 Diabetes, Delayed Motor Development and Mild Intellectual Disability
2025
·
S. Naudhani
, F. K. Bazai
, et al.
·
Russian Journal of Genetics
·
1
Detection of Two Missense Substitutions in Gene EPM2B in Patients of Myoclonic Epilepsy from Balochistan
2022
·
Akram Ali Baloch
, Adeel Ahmad
, et al.
·
Pakistan Journal of Zoology
·
1
Mutational Studies of Gene HBB in β-Thalassemia Patients from Balochistan, Pakistan
2021
·
Asma Yousafzai
, Faiza Nawaz
, et al.
·
Current Trends in OMICS
·
1
PDF
DMD Gene Mutation identification in Duchenne Muscular Dystrophy Patients of Quetta, Balochistan, Pakistan
2019
·
Muhammad Zeeshan
, Sanam Zeib Khan
, et al.
·
Biocell
·
1
Metaplastic Carcinoma of the Breast: A Clinical Study of 7 Cases from Balochistan
2014
·
Abdul Hameed Baloch
, Shakeela Daud
, et al.
·
Advances in Breast Cancer Research
·
1
PDF
A Cross-Sectional Study on the Distribution of Hemoglobin Levels Among Pregnant Women in Quetta, Balochistan
2026
·
Halima Khalid
, Sobia Faisal Malik
, et al.
·
Trends in Biological Sciences
PDF
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Works count:
35
Citation count:
292
H-index:
9
I10-index:
9
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