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Prevalence and distribution of human Plasmodium infection in Pakistan

Malaria journal, 2013-08, Vol.12 (1), p.297-297, Article 297

2013

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Role of Interleukin-6 Polymorphism in Acute Graft-Versus-Host Disease Risk Prediction in Allogeneic Hematopoietic Stem Cell Transplantation

Journal of Applied Hematology, 2022-10, Vol.13 (4), p.255-262

2022

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Screening of the FANCA gene mutational hotspots in the Pakistani fanconi anemia patients revealed 19 sequence variations

Congenital anomalies, 2020-01, Vol.60 (1), p.32-39

2020

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A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees

American journal of medical genetics. Part A, 2022-02, Vol.188 (2), p.498-508

2022

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Association of Interleukin-6 Gene Promoter Polymorphism with Coronary Artery Disease in Pakistani Families

TheScientificWorld, 2013-01, Vol.2013 (2013), p.1-6

2013

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Polymorphism in the IL-8 Gene Promoter and the Risk of Acne Vulgaris in a Pakistani Population

Iranian journal of allergy, asthma, and immunology, 2015-08, Vol.14 (4), p.443-449

2015

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Establishment of a stem cell research department through the American Society of Hematology Visitor Training Program

Blood advances, 2017-12, Vol.1 (Suppl), p.44-45

Satti, Humayoon Shafique

2017

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Epidemiological, clinical and genetic characterization of aplastic anemia patients in Pakistan

Annals of hematology, 2019-02, Vol.98 (2), p.301-312

2019

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Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

BMC medical genomics, 2021-11, Vol.14 (1), p.264-264, Article 264

2021

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Epidemiology of HIV/AIDS and Syphilis among High Risk Groups in Pakistan

Pakistan journal of zoology, 2017-10, Vol.49 (5), p.1829

2017

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A homozygous missense variant in YTHDC2 induces azoospermia in two siblings

Molecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.84, Article 84

2024

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537: CAN ARTIFICIAL INTELLIGENCE PREDICT THE DEVELOPMENT OF ABDOMINAL PAIN IN CHILDREN?

Gastroenterology (New York, N.Y. 1943), 2022-05, Vol.162 (7), p.S-125-S-125

2022

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Autologous mesenchymal stromal cell transplantation for spinal cord injury: A Phase I pilot study

Cytotherapy (Oxford, England), 2016-04, Vol.18 (4), p.518-522

2016

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Comparison of Conventional Cyclophosphamide versus Fludarabine-Based Conditioning in High-Risk Aplastic Anemia Patients Undergoing Matched-Related Donor Transplantation

Clinical hematology international, 2020, Vol.2 (2), p.82-91

2020

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The Promise of Next-Generation Sequencing in Improving the Diagnosis of Rare Genetic Disorders in Developing Countries

Blood, 2022-11, Vol.140 (Supplement 1), p.13009-13010

2022

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Identification of a homozygous variant in ABCG5 by panel sequencing in a Pakistani family with sitosterolemia: genotype-phenotype correlation and management considerations

Journal of clinical lipidology, 2024-10

2024

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Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN

Molecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.55-55, Article 55

2024

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Epidemiology of aplastic anemia: a study of 1324 cases

Hematology (Luxembourg), 2020-01, Vol.25 (1), p.48-54

2020

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Outcome of Fludarabine-Based Conditioning in High-Risk Aplastic Anemia Patients Undergoing Matched Related Donor Transplantation: A Single-Center Study from Pakistan

Biology of blood and marrow transplantation, 2019-12, Vol.25 (12), p.2375-2382

2019

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Post Allogeneic Hematopoietic Cell Transplant Erythrocytosis in Aplastic Anemia: A Review of 208 Cases

Blood, 2017-12, Vol.130, p.5499-5499

2017

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Allogeneic Haematopoietic Cell Transplantation in Aplastic Anaemia: A Dataset of 240 Cases

Blood, 2017-12, Vol.130, p.2040-2040

2017

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NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes

Molecular genetics and genomics : MGG, 2022-11, Vol.297 (6), p.1601-1613

2022

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Rabbit ATG Plus Cyclophosphamide with or without Fludarabine Is Superior Conditioning Regimen for Patients with Severe Aplastic Anemia Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Blood, 2016-12, Vol.128 (22), p.2212-2212

2016

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Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Aplastic Anemia: A Comparison of 3 Conditioning Regimens in 202 Consecutive Cases

Blood, 2014-12, Vol.124 (21), p.3881-3881

2014

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Arginase-1 Variants and the Risk of Familial Coronary Artery Disease in Subjects Originating from Pakistan

Genetic testing and molecular biomarkers, 2019-01, Vol.23 (1), p.32-38

2019

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Prevalence and distribution of human Plasmodium infection in Pakistan

Role of Interleukin-6 Polymorphism in Acute Graft-Versus-Host Disease Risk Prediction in Allogeneic Hematopoietic Stem Cell Transplantation

Screening of the FANCA gene mutational hotspots in the Pakistani fanconi anemia patients revealed 19 sequence variations

A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees

Association of Interleukin-6 Gene Promoter Polymorphism with Coronary Artery Disease in Pakistani Families

Polymorphism in the IL-8 Gene Promoter and the Risk of Acne Vulgaris in a Pakistani Population

Establishment of a stem cell research department through the American Society of Hematology Visitor Training Program

Epidemiological, clinical and genetic characterization of aplastic anemia patients in Pakistan

Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

Epidemiology of HIV/AIDS and Syphilis among High Risk Groups in Pakistan

A homozygous missense variant in YTHDC2 induces azoospermia in two siblings

537: CAN ARTIFICIAL INTELLIGENCE PREDICT THE DEVELOPMENT OF ABDOMINAL PAIN IN CHILDREN?

Autologous mesenchymal stromal cell transplantation for spinal cord injury: A Phase I pilot study

Comparison of Conventional Cyclophosphamide versus Fludarabine-Based Conditioning in High-Risk Aplastic Anemia Patients Undergoing Matched-Related Donor Transplantation

The Promise of Next-Generation Sequencing in Improving the Diagnosis of Rare Genetic Disorders in Developing Countries

Identification of a homozygous variant in ABCG5 by panel sequencing in a Pakistani family with sitosterolemia: genotype-phenotype correlation and management considerations

Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN

Epidemiology of aplastic anemia: a study of 1324 cases

Outcome of Fludarabine-Based Conditioning in High-Risk Aplastic Anemia Patients Undergoing Matched Related Donor Transplantation: A Single-Center Study from Pakistan

Post Allogeneic Hematopoietic Cell Transplant Erythrocytosis in Aplastic Anemia: A Review of 208 Cases

Allogeneic Haematopoietic Cell Transplantation in Aplastic Anaemia: A Dataset of 240 Cases

NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes

Rabbit ATG Plus Cyclophosphamide with or without Fludarabine Is Superior Conditioning Regimen for Patients with Severe Aplastic Anemia Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Aplastic Anemia: A Comparison of 3 Conditioning Regimens in 202 Consecutive Cases

Arginase-1 Variants and the Risk of Familial Coronary Artery Disease in Subjects Originating from Pakistan

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