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Khaliq, Shagufta
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1

Clinical utility of CLL-IPI scoring system in Pakistani Chr..:

Hameed, Aisha ; Nadia Sajid ; Muhammad Fayyaz.
Pakistan Journal of Medical Sciences.  40 (2024)  4 - p. , 2024
Link: https://doi.org/10.12669..
 
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2

OXGR1 is a candidate disease gene for human calcium oxalate..:

Majmundar, Amar J. ; Widmeier, Eugen ; Heneghan, John F....
Genetics in Medicine.  25 (2023)  3 - p. 100351 , 2023
Link: https://doi.org/10.1016/..
 
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3

Molecular Characterization of Haemoglobin E:

Ejaz, Sara ; Ghulam Mustafa ; Khaliq, Shagufta.
Journal of the Pakistan Medical Association.  73 (2023)  12 - p. 2357-2362 , 2023
Link: https://doi.org/10.47391..
 
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4

Genetic Alterations, DNA Methylation, Alloantibodies and Ph..:

Naveed, Muhammad Asif ; Abid, Aiysha ; Ali, Nadir...
Genes.  13 (2022)  6 - p. 971 , 2022
Link: https://doi.org/10.3390/..
 
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5

HOGA1gene pathogenic variants in primary hyperoxaluria type..:

Abid, Aiysha ; Raza, Ali ; Aziz, Tahir.
Human Mutation.  43 (2022)  12 - p. 1757-1779 , 2022
Link: https://doi.org/10.1002/..
 
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6

Primary hyperoxaluria: Comprehensive mutation screening of ..:

Abid, Aiysha ; Raza, Ali ; Khan, Abdul Rafay...
Clinical Genetics.  103 (2022)  1 - p. 53-66 , 2022
Link: https://doi.org/10.1111/..
 
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7

Association of specific single nucleotide variants (SNVs) i..:

Ajaz, Sadia ; Muneer, Rabbia ; Siddiqa, Aisha...
Oral Oncology.  122 (2021)  - p. 105519 , 2021
Link: https://doi.org/10.1016/..
 
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8

Absence of Glutathione S-Transferase Theta 1 Gene Is Signif..:

Ajaz, Sadia ; Zaidi, Sani-e-Zehra ; Ali, Saleema Mehboob...
Frontiers in Oncology.  11 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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9

Two homozygous missense mutations inITGB3gene as a cause of..:

Ali, Tooba ; Gul, Saira ; Amar, Ali...
International Journal of Laboratory Hematology.  42 (2020)  5 - p. 628-635 , 2020
Link: https://doi.org/10.1111/..
 
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10

Osteopontin promoter polymorphisms and risk of urolithiasis..:

Amar, Ali ; Afzal, Ayesha ; Hameed, Athar...
BMC Medical Genetics.  21 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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11

Gene panel sequencing identifies a likely monogenic cause i..:

Amar, Ali ; Majmundar, Amar J. ; Ullah, Ihsan...
Human Genetics.  138 (2019)  3 - p. 211-219 , 2019
Link: https://doi.org/10.1007/..
 
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12

Association analysis of the VEGF gene variants with breast ..:

Ajaz, Sadia ; Siddiqa, Aisha ; Ali, Saleema Mehboob...
Gene Reports.  16 (2019)  - p. 100447 , 2019
Link: https://doi.org/10.1016/..
 
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13

Association of vitamin D receptor gene polymorphisms and ri..:

Amar, Ali ; Afzal, Ayesha ; Hussain, Syed Atif...
Urolithiasis.  48 (2019)  5 - p. 385-401 , 2019
Link: https://doi.org/10.1007/..
 
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14

Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pedi..:

Abid, Aiysha ; Shahid, Saba ; Shakoor, Madiha...
Frontiers in Genetics.  9 (2018)  - p. , 2018
Link: https://doi.org/10.3389/..
 
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15

"Like sugar in milk": reconstructing the genetic history of..:

Chaubey, Gyaneshwer ; Ayub, Qasim ; Rai, Niraj...
Genome Biology.  18 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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