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Mariam Khanfar
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SLC30A8 gene polymorphism rs13266634 associated with increased risk for developing type 2 diabetes mellitus in Jordanian population
S Mashal, M Khanfar, S Al-Khalayfa, L Srour, L Mustafa, NM Hakooz, ...
Gene 768, 145279, 2021
212021
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase
K Krysiak, AM Danos, J Saliba, JF McMichael, AC Coffman, S Kiwala, ...
Nucleic acids research 51 (D1), D1230-D1241, 2023
112023
Computational genomics in the era of precision medicine: applications to variant analysis and gene therapy
YC Wang, Y Wu, J Choi, G Allington, S Zhao, M Khanfar, K Yang, PY Fu, ...
Journal of Personalized Medicine 12 (2), 175, 2022
102022
Evaluation of patched-1 protein expression level in low risk and high risk basal cell carcinoma subtypes
R Almomani, M Khanfar, K Bodoor, F Al-Qarqaz, M Alqudah, H Hammouri, ...
Asian Pacific Journal of Cancer Prevention: APJCP 20 (9), 2851, 2019
72019
Leptin and the GA genotype of rs2167270 of the LEP gene increase the risk of prediabetes
MA Aljanabi, MA Alfaqih, M Khanfar, ZO Amarin, L Elsalem, R Saadeh, ...
Biomedical Reports 14 (5), 1-8, 2021
62021
Association of vitamin D levels and polymorphisms in vitamin D receptor with type 2 diabetes mellitus
MA Alfaqih, A Araidah, Z Amarin, R Saadeh, O Al-Shboul, M Khanfar, ...
Biomedical Reports 18 (1), 1-10, 2023
52023
Correlation between vitamin D and serum brain derived neurotropic factor levels in type 2 diabetes mellitus patients
M Alqudah, M Khanfar, MA Alfaqih, O Al‑Shboul, DG Al‑U'datt, A Al‑Dwairi, ...
Biomedical Reports 16 (6), 1-6, 2022
42022
Association of E23K (rs5219) polymorphism in the KCNJ11 gene with type 2 diabetes mellitus risk in Jordanian population
S Al-Khalayfa, S Mashal, M Khanfar, L Srour, L Mustafa, A Battah, ...
Human Gene 37, 201201, 2023
22023
Maximal Aerobic Effort Increases Genetic Expression of HSP90AA1, HSP90AB1, and PTGES3 in Elite Taekwondo Athletes
R Hammad, L Srour, S Hammad, A Abubaker, R Zaza, D Aburizeg, ...
Human Physiology 48 (3), 254-260, 2022
22022
A single nucleotide polymorphism in BCAT1 gene is associated with type 2 diabetes mellitus
MA Alfaqih, ZE Abu-Khdair, O Khabour, KA Kheirallah, M Khanfar
Acta Biochimica Polonica 69 (1), 19-24, 2022
22022
A homozygous variant in ABCA3 is associated with severe respiratory distress and early neonatal death
M Al‐Iede, M Khanfar, L Srour, R Rabah, M Al‐Abbadi, B Azab, ...
John Wiley & Sons Australia, Ltd, 2021
12021
Effect of genetic testing on diagnosing gastrointestinal pediatric patients with previously undiagnosed diseases
E Altamimi, M Khanfar, O Rabab’h, Z Dardas, L Srour, L Mustafa, B Azab
The application of clinical genetics, 221-231, 2020
12020
P085: Addition of new variant classes to the CIViC data model
A Danos, K Krysiak, J Saliba, A Coffman, S Kiwala, J McMichael, ...
Genetics in Medicine Open 2, 2024
2024
35. Evolution of a variant curation procedures in the open-access cancer variant interpretation knowledgebase CIViC
K Krysiak, A Danos, J Saliba, S Kiwala, A Coffman, J McMichael, ...
Cancer Genetics 278, 11, 2023
2023
19. Developing a generalized model for variants in CIViC
A Danos, K Krysiak, J Saliba, S Kiwala, J McMichael, A Coffman, ...
Cancer Genetics 278, 6, 2023
2023
57. Curating variants of established clinical significance
M Khanfar, A Danos, J Saliba, AE Kovach, CJ Grisdale, C Mullighan, ...
Cancer Genetics 278, 18, 2023
2023
Leptin and the rs2167270 Polymorphism Are Associated with Glycemic Control in Type Two Diabetes Mellitus Patients on Metformin Therapy
MA Alfaqih, M Aljanabi, E Ababneh, M Khanfar, M Alqudah, M Sater
Medicina 59 (5), 997, 2023
2023
Leptin reduces the risk of poor glycemic control in type two diabetes mellitus patients on metformin therapy
MA Alfaqih, M Aljanabi, E Ababneh, M Khanfar, M Sater
Endocrine Abstracts 90, 2023
2023
Supporting Evolving Clinical Guidelines Requires Updated Cancer Variant Interpretation Resources
K Krysiak, A Coffman, S Kiwala, J McMichael, A Danos, J Saliba, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 24 (10), S17-S17, 2022
2022
Utilizing Whole Exome Sequencing Reveals a Rare Inherited Variant in ABCA3 Gene
M Al-Iede, M Khanfar, L Srour, R Rabah, M Al-Abbadi, B Azab, E Badran
Authorea Preprints, 2020
2020
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