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Secured Dynamic Request Scheduling and Optimal CSP Selection for Analyzing Cloud Service Performance Using Intelligent Approaches

IEEE access, 2023, Vol.11, p.140914-140933

2023

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Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

Frontiers in genetics, 2024-08, Vol.15

2024

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Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein‐truncating mutations of ASPM

Biotechnology and applied biochemistry, 2022-12, Vol.69 (6), p.2296-2303

2022

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Machine Learning Approach to Classification of Online Users by Exploiting Information Seeking Behavior

IEEE access, 2024, Vol.12, p.53234-53249

2024

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Current updates on genetic spectrum of usher syndrome

Nucleosides, nucleotides & nucleic acids, 2024-05, p.1-24

2024

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Comment on homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene

International journal of ophthalmology, 2017-05

2017

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The molecular genetics of UV-Sensitive syndrome: A rare dermal anomaly

Journal of the Pakistan Medical Association, 2021-10, Vol.71 (10), p.2391-2396

2021

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Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms

Frontiers in neurology, 2023-05, Vol.14, p.1168307-1168307

2023

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UHPLC, ATR-FTIR analysis of Nymphoides indica rhizome extract and determination of antioxidant & antibiofilm potential

Main group chemistry, 2022-01, Vol.21 (1), p.157-166

2022

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A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family

Frontiers in endocrinology (Lausanne), 2023-03, Vol.14, p.1066182-1066182

2023

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Development and Evaluation of Essential Oil-Based Nanoemulgel Formulation for the Treatment of Oral Bacterial Infections

Gels, 2023-03, Vol.9 (3), p.252

2023

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A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family

Basic and clinical andrology, 2024-02, Vol.34 (1), p.4-4, Article 4

2024

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Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans

Journal of Taibah University for Science, 2023-12, Vol.17 (1)

2023

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A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome

Bone Reports, 2024-09, Vol.22, p.101789, Article 101789

2024

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Lumateperone Interact with S-Protein of Ebola Virus and TIM-1 of Human Cell Membrane: Insights from Computational Studies

Applied sciences, 2022-09, Vol.12 (17), p.8820

2022

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Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene

Pakistan journal of zoology, 2022-06, Vol.54 (3), p.1215

2022

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CHONDROMATOUS MASS ON LOWER FOREARM

Gomal journal of medical sciences, 2017-12, Vol.15 (2)

2017

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Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice

JCI insight, 2023-02, Vol.8 (3)

2023

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Survey of Plant Parasitic Nematodes in Different Regions of Khyber- Pakhtun-Khwa

Pakistan journal of zoology, 2015-08, Vol.47 (4)

2015

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Prioritization of Disease Prone Exons in INPP5E Gene, Associated With Joubert Syndrome, by in silico Analysis of Non-Synonymous SNPs

Pakistan journal of zoology, 2015-06, Vol.47 (3)

2015

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CLINICAL PRESENTATION OF AN EXTENDED CONSANGUINEOUS FAMILY INHERITING WOOLLY HAIR HYPOTRICHOSIS

Gomal journal of medical sciences, 2018-12, Vol.16 (1), p.24

Khan, Muzammil Ahmad

2018

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IMAGES IN CLINICAL MEDICINE

Gomal journal of medical sciences, 2018-03, Vol.16 (1), p.24

2018

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MICROPHTHALMIA: AN IMPORTANT GENETIC EYE DISORDER

Gomal journal of medical sciences, 2017-01, Vol.14 (3)

Muzammil Ahmad Khan

2017

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Virtual 3D Tour: A User Experience for On-Campus Orientation

Pakistan Journal of Scientific Research, 2023-07, Vol.3 (1), p.32-37

2023

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Genetic basis of ß-thalassemia in families of pashtun ethnicity in Dera Ismail Khan district of Khyber Pakhtun-Khwa province, Pakistan

Expert review of hematology, 2023-09, Vol.16 (9), p.693-699

2023

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Secured Dynamic Request Scheduling and Optimal CSP Selection for Analyzing Cloud Service Performance Using Intelligent Approaches

Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein‐truncating mutations of ASPM

Machine Learning Approach to Classification of Online Users by Exploiting Information Seeking Behavior

Current updates on genetic spectrum of usher syndrome

Comment on homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene

The molecular genetics of UV-Sensitive syndrome: A rare dermal anomaly

Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms

UHPLC, ATR-FTIR analysis of Nymphoides indica rhizome extract and determination of antioxidant & antibiofilm potential

A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family

Development and Evaluation of Essential Oil-Based Nanoemulgel Formulation for the Treatment of Oral Bacterial Infections

A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family

Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans

A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome

Lumateperone Interact with S-Protein of Ebola Virus and TIM-1 of Human Cell Membrane: Insights from Computational Studies

Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene

CHONDROMATOUS MASS ON LOWER FOREARM

Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice

Survey of Plant Parasitic Nematodes in Different Regions of Khyber- Pakhtun-Khwa

Prioritization of Disease Prone Exons in INPP5E Gene, Associated With Joubert Syndrome, by in silico Analysis of Non-Synonymous SNPs

CLINICAL PRESENTATION OF AN EXTENDED CONSANGUINEOUS FAMILY INHERITING WOOLLY HAIR HYPOTRICHOSIS

IMAGES IN CLINICAL MEDICINE

MICROPHTHALMIA: AN IMPORTANT GENETIC EYE DISORDER

Virtual 3D Tour: A User Experience for On-Campus Orientation

Genetic basis of ß-thalassemia in families of pashtun ethnicity in Dera Ismail Khan district of Khyber Pakhtun-Khwa province, Pakistan

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