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Exonic Deletion in MAN1B1 and a Missense Substitution in CAPN10 Causes Truncal Obesity, Type 2 Diabetes, Delayed Motor Development and Mild Intellectual Disability
S Naudhani, FK Bazai, A Ahmad, H Tayyab, MT Pervez, A Zafar, SA Shah, N Raheem, M Tariq, M Saleem, R Sheikh, S Daud
(2025)
Russian Journal of Genetics
vol.
61
no.
6
pp.
726-735
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Targeted Sequencing of HEXA Gene Shows Missense Substitution (p.Arg499His) in a Large Pakistani Family with Tay-Sachs Disease
Fariya Khan Bazai, Mehmood Ul Hassan, Hani Tayyab, Sara Naudhani, Sami Siraj, Muhammad Tariq, Sajjad Ali Shah, Jamil Ahmad, Shakeela Daud
(2024)
Cytology and Genetics
vol.
58
no.
5
pp.
486-492
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A Missense Pathogenic Variant in a Conserved Region of CNTNAP2 Is Associated with Obesity, Seizures, and Language Impairment in a Pakistani Family
Sara Naudhani, Adeel Ahmad, Fariya Khan Bazai, Muhammad Tariq Pervez, Azqa Zafar, Sajjad Ali Shah, Nafeesa Raheem, Abdul Hameed Baloch, Muhammad Mushtaq, Shakeela Daud
(2023)
Molecular Syndromology
vol.
14
no.
4
pp.
293-302
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Molecular Medicine Communications
Sara Naudhani, Fariya Khan Bazai, Akram Ali Mehmood Ul Hassan, Hani Tayyab, Sara Mannan, Muhammad Tariq, Shakeela Daud
(2023)
-
vol.
-
no.
-
pp.
-
|
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Detection of Two Missense Substitutions in Gene EPM2B in Patients of Myoclonic Epilepsy from Balochistan
Akram Ali Baloch, Adeel Ahmad, Kaleem U Kakar, Sara Naudhani, Samiullah Khan, Muhammad Raza Agha, Imrana Niaz Sultan, Humaira Zahid, Shakeela Daud
(2023)
Pakistan Journal of Zoology
vol.
55
no.
6
pp.
2683
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Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family
Abdulhadi Almazroea, Ambreen Ijaz, Abdul Aziz, Muhammad Mushtaq Yasinzai, Rafiullah Rafiullah, Fazal Ur Rehman, Shakeela Daud, Rozeena Shaikh, Muhammad Ayub, Abdul Wali
(2023)
Medicina
vol.
59
no.
1
pp.
103
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corrected Proof
Muhammad Luqman, Muhammad Umer Farooq Awan, Sohaib Muhammad, Shakeela Daud, Asma Yousafzai, Fariha Aroojaa
(2022)
-
vol.
-
no.
-
pp.
-
|
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Detection of Two Missense Substitutions in Gene EPM2B in Patients of Myoclonic Epilepsy from Balochistan.
Saadullah and Shakeela Daud. Akram Ali Baloch1 , Adeel Ahmad , Kaleem U. Kakar , Sara Naudhani , Samiullah Khan , Agha Muhammad Raza , Imrana Niaz Sultan , Humaira Zahid
(2022)
Pakistan Journal of Zoology.
vol.
54
no.
4
pp.
1-6
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Genetic data of 22 autosomal STR loci in Khyber-Pakhtunkhwa, Balochistan and Gilgit Baltistan population of Pakistan using PowerPlex® fusion system.
Shahid A. Shafique M, Sajid N, Aziz Y,Afzal M, Shahzad M, Shehzadi A, Bashir S,Daud S
(2022)
Legal Medicine.
vol.
59
no.
-
pp.
1021-29.
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Nested-PCR based Detection of Hepatitis C Virus: Low-cost Strategy in Pakistan: Nested-PCR based detection of Hepatitis C virus
Rabia Javeed, Nabeela Tariq, Shakeela Daud, Asma Yousafzai, Saba Manzoor, Adeel Ahmad
(2022)
Proceedings of the Pakistan Academy of Sciences: B. Life and Environmental Sciences
vol.
59
no.
3
pp.
81-87
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Mutational Analysis of Gene BRD2 in Patients of Juvenile Myoclonic Epilepsy
Shakeela Daud, Saba Manzoor, Adeel Ahmad, Palwasha Khan, Asma Yousafzai, Nabeela Tariq, Muhammad Luqman, Gohram Khan
(2022)
International Journal of Pathology
vol.
-
no.
-
pp.
7-13
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A. Study on Amyotrophic lateral Sclerosis: A Disease of Motor Neuron in Pakistan.
Daud S Yousafzai A
(2022)
Int.j.pathol.
vol.
19
no.
3
pp.
155-164.
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Microbial pollution in inland recreational freshwaters of Quetta, Pakistan: an initial report.
Arooj F. Luqman M, Awan MUF, Muhammad S, Daud S, Yousafzai A
(2022)
J Water Health.
vol.
20
no.
3
pp.
575-588
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Mutational Studies of Gene HBB in β-Thalassemia Patients from Balochistan, Pakistan.
S. Nawaz, F., Yousafzai, A., Luqman, M., Ahmed, N., Arbab, M., Tabassum, J., Ahmad, J., & Daud
(2021)
Current Trends in OMICS.
vol.
1
no.
2
pp.
80-94.
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ESTIMATION OF ALLELE’S FREQUENCY OF FOUR STR MARKERS (D5S818, D7S820, D13S317 & D16S539) IN PASHTUN POPULATION IN BALOCHISTAN, PAKISTAN
Palwasha Khan, Shakeela Daud, Asma Abro, Nida Ajmal, Saira Jamali
(2021)
-
vol.
18
no.
2
pp.
275-279
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Mutational Analysis of Gene BRD2 in Patients of Juvenile Myoclonic Epilepsy.
Muhammad Luqman andGohramKhan. Hidayetullah,ShakeelaDaud, Saba Manzoor, Adeel Ahmad, Palwasha Khan,Asma Yousafzai, Nabeela Tariq
(2021)
Int.j.pathol.
vol.
20
no.
1
pp.
7-13.
|
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Estimation of Allele’s Frequency of four STR markers (D5S818,D7S820, D13S317 & D16S539) in Pashtun Population in Balochistan, Pakistan.
Ajmal N and Jamali S. Khan P*, Daud S, Abro A
(2021)
Int. Biol. Biotech.
vol.
18
no.
2
pp.
275-279.
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Study on amyotrophic lateral sclerosis: a disease of motor neuron in Pakistan
Shakeela Daud, Asma Yousafzai
(2021)
International Journal of Pathology
vol.
-
no.
-
pp.
155-164
|
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Identification of Mutations in Gene BRCA1/2 in Breast Cancer Cases from Balochistan.
Javed M.M and Ahmad J. Yousafzai A, Luqman M, Ahmed N, Arbab M, Murad M, Sajjad N, Naudhani N, Daud S, Baloch AH, Khushnaseeb, Zahoor S, Rauf Z
(2019)
Pakistan J. Zool.
vol.
51
no.
4
pp.
1579-1582.
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In-Silico Analysis of Gene ALS2 Genetic Variants Identified in affected Horses and Humans with Motor Neuron Disease.
Umar S. Daud S, Ahmed N, Naudhani S, Younus M, Manzoor S, Firyal S, Yaqub T, Hashmi A.S, Riaz UlAmin, Wasim M
(2018)
Jevs.
vol.
62
no.
-
pp.
60-65
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