Solaf Elsayed

About Solaf Elsayed

Solaf Elsayed, With an exceptional h-index of 19 and a recent h-index of 15 (since 2020), a distinguished researcher at Ain Shams University, specializes in the field of Medical genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Metabolic and other morbid complications in congenital generalized lipodystrophy type 4

SAT292 Adrenal Insufficiency Associated With Biallelic Mutations In Porphyria Genes

Another Chanarin-Dorfman Syndrome (CDS) in an Egyptian Patient

Difficult Diagnosis in a Patient with Phenylketonuria (PKU) and Metachromatic Leukodystrophy (MLD)

Adrenal Insufficiency Associated with Biallelic Mutations in Porphyria Genes

A novel ABHD5 mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype

5613463 PREVALENCE OF HEMOCHROMATOSIS HFE GENE POLYMORPHISM AMONG EGYPTIAN βTHALASSEMIA PATIENTS AND ITS RELATION TO DEVELOPMENT OF DIABETES MELLITUS

Extra-hepatic portal vein thrombosis in children: Single center experience

Solaf Elsayed Information

University

Position

Professor of medical genetics Genetics Unit

Citations(all)

2036

Citations(since 2020)

1026

Cited By

1308

hIndex(all)

19

hIndex(since 2020)

15

i10Index(all)

36

i10Index(since 2020)

23

Email

University Profile Page

Google Scholar

Solaf Elsayed Skills & Research Interests

Medical genetics

Top articles of Solaf Elsayed

Metabolic and other morbid complications in congenital generalized lipodystrophy type 4

American Journal of Medical Genetics Part A

2024/1/17

SAT292 Adrenal Insufficiency Associated With Biallelic Mutations In Porphyria Genes

Journal of the Endocrine Society

2023/10

Another Chanarin-Dorfman Syndrome (CDS) in an Egyptian Patient

QJM: An International Journal of Medicine

2023/6/1

Difficult Diagnosis in a Patient with Phenylketonuria (PKU) and Metachromatic Leukodystrophy (MLD)

QJM: An International Journal of Medicine

2023/6/1

Adrenal Insufficiency Associated with Biallelic Mutations in Porphyria Genes

Endocrine Abstracts

2023/5/2

A novel ABHD5 mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype

Genes & Diseases

2023/5

5613463 PREVALENCE OF HEMOCHROMATOSIS HFE GENE POLYMORPHISM AMONG EGYPTIAN βTHALASSEMIA PATIENTS AND ITS RELATION TO DEVELOPMENT OF DIABETES MELLITUS

HemaSphere

2023/4/1

Extra-hepatic portal vein thrombosis in children: Single center experience

Clinical and Experimental Hepatology

2023/3/1

ALL-124 Outcome of Acute Leukemia in Down Syndrome: A Retrospective Experience of Ain Shams Pediatric Oncology Over a Decade

Clinical Lymphoma Myeloma and Leukemia

2022/10/1

An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

European Journal of Human Genetics

2022/9

Multicentric osteolysis, nodulosis, and arthropathy in 2 unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations.

Saudi Medical Journal

2022/6/1

PB1939: CLINICAL AND GENETIC CHARACTERISTICS OF PATIENTS WITH GAUCHER DISEASE: A SINGLE CENTER EXPERIENCE

HemaSphere

2022/6/1

Solaf Elsayed
Solaf Elsayed

H-Index: 13

Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency

Journal of Medical Genetics

2022/4/1

Solaf Elsayed
Solaf Elsayed

H-Index: 13

Professor Rabah Mohamed Shawky, 1943–2021

2021/12

Skeletal radiology following hematopoietic stem cell transplantation in infantile osteopetrosis: an overlooked assessment tool

Boletín médico del Hospital Infantil de México

2021/10

MPI‐CDG from a hepatic perspective: Report of two Egyptian cases and review of literature

2020/11

A rare type of skeletal dysplasia resembling rheumatoid arthritis

QJM: An International Journal of Medicine

2020/3/1

See List of Professors in Solaf Elsayed University(Ain Shams University)