Ahmed Alfares

Ahmed Alfares

Qassim University

H-index: 19

Asia-Saudi Arabia

About Ahmed Alfares

Ahmed Alfares, With an exceptional h-index of 19 and a recent h-index of 18 (since 2020), a distinguished researcher at Qassim University, specializes in the field of Genetics.

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

Untargeted metabolomics reveals novel biomarkers and altered pathways in maple syrup urine disease: A noninvasive approach for early diagnosis in newborns

Molecular Characterisation and Outcomes of 363 Adolescent and Young Adults with AML in Saudi Arabia Risk Stratified By PCR and NGS-Based Testing

Prospect of genetic disorders in Saudi Arabia

Supplementary testing after negative or inconclusive exome sequencing results

The diagnostic yield of CGH and WES in neurodevelopmental disorders

Genetic impact of non-consanguineous marriages in Saudi Arabia

The variant artificial intelligence easy scoring (VARIES) system

HMG-CoA lyase deficiency: A retrospective study of 62 Saudi patients

Ahmed Alfares Information

University

Position

___

Citations(all)

1857

Citations(since 2020)

1413

Cited By

852

hIndex(all)

19

hIndex(since 2020)

18

i10Index(all)

26

i10Index(since 2020)

25

Email

University Profile Page

Google Scholar

Ahmed Alfares Skills & Research Interests

Genetics

Top articles of Ahmed Alfares

Untargeted metabolomics reveals novel biomarkers and altered pathways in maple syrup urine disease: A noninvasive approach for early diagnosis in newborns

Molecular Genetics and Metabolism

2024/4/1

Ahmed Alfares
Ahmed Alfares

H-Index: 11

Molecular Characterisation and Outcomes of 363 Adolescent and Young Adults with AML in Saudi Arabia Risk Stratified By PCR and NGS-Based Testing

Blood

2023/12/1

Prospect of genetic disorders in Saudi Arabia

Frontiers in Genetics

2023/9/20

Fahad Almsned
Fahad Almsned

H-Index: 3

Ahmed Alfares
Ahmed Alfares

H-Index: 11

Supplementary testing after negative or inconclusive exome sequencing results

Journal of Biochemical and Clinical Genetics

2023/3/30

The diagnostic yield of CGH and WES in neurodevelopmental disorders

Frontiers in Pediatrics

2023/3/1

Ahmed Alfares
Ahmed Alfares

H-Index: 11

Genetic impact of non-consanguineous marriages in Saudi Arabia

2022/7/29

Ahmed Alfares
Ahmed Alfares

H-Index: 11

The variant artificial intelligence easy scoring (VARIES) system

Computers in Biology and Medicine

2022/6/1

Abdulrhman Aljouie
Abdulrhman Aljouie

H-Index: 3

Ahmed Alfares
Ahmed Alfares

H-Index: 11

HMG-CoA lyase deficiency: A retrospective study of 62 Saudi patients

Frontiers in Genetics

2022/5/13

The morbid genome of ciliopathies: an update

Genetics in Medicine

2022/4/1

DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning

Bioinformatics

2022/3/15

Cut-off values in newborn screening for inborn errors of metabolism in Saudi Arabia

Annals of Saudi Medicine

2022/3

Ahmed Alfares
Ahmed Alfares

H-Index: 11

Common disease-associated gene variants in a Saudi Arabian population

Annals of Saudi Medicine

2022/1

Ahmed Alfares
Ahmed Alfares

H-Index: 11

The rate of secondary genomic findings in the Saudi population

American Journal of Medical Genetics Part A

2022/1

Ahmed Alfares
Ahmed Alfares

H-Index: 11

The leukodystrophy spectrum in Saudi Arabia: Epidemiological, clinical, radiological, and genetic data

Frontiers in Pediatrics

2021/5/13

Amended Informative Negative Whole Exome Sequencing Results

2021/1/19

Ahmed Alfares
Ahmed Alfares

H-Index: 11

Successful application of genome sequencing in a diagnostic setting: 1007 index cases from a clinically heterogeneous cohort

European Journal of Human Genetics

2021/1

Two Novel Homozygous HPS6 Mutations (Double Mutant) Identified by Whole-Exome Sequencing in a Saudi Consanguineous Family Suspected for …

Life

2021/12/23

Ahmed Alfares
Ahmed Alfares

H-Index: 11

Long-term effectiveness of carglumic acid in patients with propionic acidemia (PA) and methylmalonic acidemia (MMA): a randomized clinical trial

Orphanet Journal of Rare Diseases

2021/12

Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

Genome Medicine

2021/12

Gabrielle Wheway
Gabrielle Wheway

H-Index: 16

Ahmed Alfares
Ahmed Alfares

H-Index: 11

See List of Professors in Ahmed Alfares University(Qassim University)