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1
cxsAssociation study between single nucleotide polymorphism in thrombospondins THBS1 gene and THBS2 gene and coronary artery disease in Indian population
cxsAssociation study between single nucleotide polymorphism in thrombospondins THBS1 gene and THBS2 gene and coronary artery disease in Indian population
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cxsAssociation study between single nucleotide polymorphism in thrombospondins THBS1 gene and THBS2 gene and coronary artery disease in Indian population

Egyptian Journal of Medical Human Genetics, 2024-02, Vol.25 (1), p.26-8 [Peer Reviewed Journal]

The Author(s) 2024 ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00498-2

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2
Cataloging the potential SNPs (single nucleotide polymorphisms) associated with quantitative traits, viz. BMI (body mass index), IQ (intelligence quotient) and BP (blood pressure): an updated review
Cataloging the potential SNPs (single nucleotide polymorphisms) associated with quantitative traits, viz. BMI (body mass index), IQ (intelligence quotient) and BP (blood pressure): an updated review
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Cataloging the potential SNPs (single nucleotide polymorphisms) associated with quantitative traits, viz. BMI (body mass index), IQ (intelligence quotient) and BP (blood pressure): an updated review

Egyptian Journal of Medical Human Genetics, 2022-03, Vol.23 (1), p.1-24 [Peer Reviewed Journal]

The Author(s) 2022 ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00266-0

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3
Association of ABCA1 gene with Coronary Artery Disease (CAD): an overview
Association of ABCA1 gene with Coronary Artery Disease (CAD): an overview
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Association of ABCA1 gene with Coronary Artery Disease (CAD): an overview

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.74-8 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00440-y

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4
Intellectual developmental disorder with dysmorphic facies and ptosis caused by copy number variation including the BRPF1 gene in Peruvian patient
Intellectual developmental disorder with dysmorphic facies and ptosis caused by copy number variation including the BRPF1 gene in Peruvian patient
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Intellectual developmental disorder with dysmorphic facies and ptosis caused by copy number variation including the BRPF1 gene in Peruvian patient

Egyptian Journal of Medical Human Genetics, 2022-12, Vol.23 (1), p.1-6 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00356-z

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5
Clinical implications of PON1 (rs662) and TNF-α (rs1799964) genes polymorphism in patients with coronary artery disease
Clinical implications of PON1 (rs662) and TNF-α (rs1799964) genes polymorphism in patients with coronary artery disease
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Clinical implications of PON1 (rs662) and TNF-α (rs1799964) genes polymorphism in patients with coronary artery disease

Egyptian Journal of Medical Human Genetics, 2022-07, Vol.23 (1), p.1-7 [Peer Reviewed Journal]

The Author(s) 2022 ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00318-5

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6
Circulating expression patterns of TL1A and FFAR2 in patients with stable and unstable angina
Circulating expression patterns of TL1A and FFAR2 in patients with stable and unstable angina
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Circulating expression patterns of TL1A and FFAR2 in patients with stable and unstable angina

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.4-9 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00386-1

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7
The association of apolipoprotein-E (APOE) gene polymorphisms with coronary artery disease: a systematic review and meta-analysis
The association of apolipoprotein-E (APOE) gene polymorphisms with coronary artery disease: a systematic review and meta-analysis
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The association of apolipoprotein-E (APOE) gene polymorphisms with coronary artery disease: a systematic review and meta-analysis

Egyptian Journal of Medical Human Genetics, 2021-03, Vol.22 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2021 ;COPYRIGHT 2021 Springer ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-021-00135-2

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8
Association of methylation status of ABCA1/G1 genes with the risk of coronary artery disease
Association of methylation status of ABCA1/G1 genes with the risk of coronary artery disease
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Association of methylation status of ABCA1/G1 genes with the risk of coronary artery disease

Egyptian Journal of Medical Human Genetics, 2022-12, Vol.23 (1), p.167-10 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00381-y

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9
Global distribution of consanguinity and their impact on complex diseases: Genetic disorders from an endogamous population
Global distribution of consanguinity and their impact on complex diseases: Genetic disorders from an endogamous population
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Global distribution of consanguinity and their impact on complex diseases: Genetic disorders from an endogamous population

The Egyptian journal of medical human genetics, 2017-10, Vol.18 (4), p.315-320 [Peer Reviewed Journal]

2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Oct 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.01.002

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10
Hematological indices in pediatric patients with acyanotic congenital heart disease: a cross-sectional study of 248 patients
Hematological indices in pediatric patients with acyanotic congenital heart disease: a cross-sectional study of 248 patients
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Hematological indices in pediatric patients with acyanotic congenital heart disease: a cross-sectional study of 248 patients

Egyptian Journal of Medical Human Genetics, 2022-03, Vol.23 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00262-4

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11
Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways
Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways
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Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways

Egyptian Journal of Medical Human Genetics, 2020-02, Vol.21 (1), p.1-12 [Peer Reviewed Journal]

The Author(s) 2020 ;COPYRIGHT 2020 Springer ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-020-0050-1

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12
Association of the ANGPTL3 gene polymorphisms and haplotypes with cardiovascular diseases in Birjand longitudinal aging study (BLAS)
Association of the ANGPTL3 gene polymorphisms and haplotypes with cardiovascular diseases in Birjand longitudinal aging study (BLAS)
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Association of the ANGPTL3 gene polymorphisms and haplotypes with cardiovascular diseases in Birjand longitudinal aging study (BLAS)

Egyptian Journal of Medical Human Genetics, 2022-12, Vol.23 (1), p.161-9 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00366-x

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13
Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene
Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene
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Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene

Egyptian Journal of Medical Human Genetics, 2022-03, Vol.23 (1), p.28-9 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00241-9

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14
Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype
Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype
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Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype

Egyptian Journal of Medical Human Genetics, 2021-03, Vol.22 (1), p.1-7 [Peer Reviewed Journal]

The Author(s) 2021 ;COPYRIGHT 2021 Springer ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-021-00136-1

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15
Association between PON1 rs662 gene polymorphism and serum paraoxonase1 level in coronary artery disease patients in Northern India
Association between PON1 rs662 gene polymorphism and serum paraoxonase1 level in coronary artery disease patients in Northern India
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Association between PON1 rs662 gene polymorphism and serum paraoxonase1 level in coronary artery disease patients in Northern India

Egyptian Journal of Medical Human Genetics, 2021-09, Vol.22 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2021 ;COPYRIGHT 2021 Springer ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-021-00196-3

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16
Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotype
Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotype
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Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotype

Egyptian Journal of Medical Human Genetics, 2020-11, Vol.21 (1) [Peer Reviewed Journal]

The Author(s) 2020 ;COPYRIGHT 2020 Springer ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-020-00093-1

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17
The β fibrinogen gene G-455A polymorphism in Asian subjects with coronary heart disease: A meta analysis
The β fibrinogen gene G-455A polymorphism in Asian subjects with coronary heart disease: A meta analysis
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The β fibrinogen gene G-455A polymorphism in Asian subjects with coronary heart disease: A meta analysis

The Egyptian journal of medical human genetics, 2017-01, Vol.18 (1), p.19-28 [Peer Reviewed Journal]

2016 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2016.06.002

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18
Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects
Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects
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Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

Egyptian Journal of Medical Human Genetics, 2020-10, Vol.21 (1), p.1-10 [Peer Reviewed Journal]

The Author(s) 2020 ;COPYRIGHT 2020 Springer ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-020-00101-4

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19
Prediction and in silico validation of MYH7 gene missense variants in the Iranian population: a bioinformatics analysis based on Iranome database
Prediction and in silico validation of MYH7 gene missense variants in the Iranian population: a bioinformatics analysis based on Iranome database
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Prediction and in silico validation of MYH7 gene missense variants in the Iranian population: a bioinformatics analysis based on Iranome database

Egyptian Journal of Medical Human Genetics, 2020-04, Vol.21 (1), p.1-7 [Peer Reviewed Journal]

The Author(s) 2020 ;COPYRIGHT 2020 Springer ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-020-00058-4

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20
Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in Iran
Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in Iran
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Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in Iran

The Egyptian journal of medical human genetics, 2018-01, Vol.19 (1), p.31-35 [Peer Reviewed Journal]

2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 2018 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.06.005

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