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1
Diagnostic biomarkers for ST-segment elevation myocardial infarction using RNA methylation regulators
Diagnostic biomarkers for ST-segment elevation myocardial infarction using RNA methylation regulators
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Diagnostic biomarkers for ST-segment elevation myocardial infarction using RNA methylation regulators

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.62-9 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;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/s43042-024-00532-3

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2
Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey
Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey
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Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.27-12 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;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/s43042-024-00490-w

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3
Association of common variant rs9934336 of SLC5A2 (SGLT2) gene with SARS-CoV-2 infection and mortality
Association of common variant rs9934336 of SLC5A2 (SGLT2) gene with SARS-CoV-2 infection and mortality
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Association of common variant rs9934336 of SLC5A2 (SGLT2) gene with SARS-CoV-2 infection and mortality

Egyptian Journal of Medical Human Genetics, 2024-01, Vol.25 (1), p.10-7 [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/s43042-024-00481-x

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4
Genetics of type 2 diabetes mellitus in Indian and Global Population: A Review
Genetics of type 2 diabetes mellitus in Indian and Global Population: A Review
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Genetics of type 2 diabetes mellitus in Indian and Global Population: A Review

Egyptian Journal of Medical Human Genetics, 2022-01, Vol.23 (1), p.1-16 [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/s43042-022-00346-1

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5
Cytogenetical analysis in blood lymphocytes of cigarette smokers in Tiruchirappalli district, Tamil Nadu, India
Cytogenetical analysis in blood lymphocytes of cigarette smokers in Tiruchirappalli district, Tamil Nadu, India
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Cytogenetical analysis in blood lymphocytes of cigarette smokers in Tiruchirappalli district, Tamil Nadu, India

The Egyptian journal of medical human genetics, 2017-04, Vol.18 (2), p.147-152 [Peer Reviewed Journal]

2016 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Apr 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2016.05.003

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6
Association study of APOE gene polymorphisms with diabetes and the main cardiometabolic risk factors, in the Algerian population
Association study of APOE gene polymorphisms with diabetes and the main cardiometabolic risk factors, in the Algerian population
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Association study of APOE gene polymorphisms with diabetes and the main cardiometabolic risk factors, in the Algerian population

Egyptian Journal of Medical Human Genetics, 2019-08, Vol.20 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2019 ;COPYRIGHT 2019 Springer ;The Author(s) 2019. 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/s43042-019-0013-6

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7
Association of genetic polymorphisms of PON1 and CETP with the presence of metabolic syndrome; the effects of genotypes on their serum activity and concentrations
Association of genetic polymorphisms of PON1 and CETP with the presence of metabolic syndrome; the effects of genotypes on their serum activity and concentrations
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Association of genetic polymorphisms of PON1 and CETP with the presence of metabolic syndrome; the effects of genotypes on their serum activity and concentrations

The Egyptian journal of medical human genetics, 2018-01, Vol.19 (1), p.43-48 [Peer Reviewed Journal]

2018 ;Copyright Egyptian Society of Medical Human Genetics Jan 2018 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.12.001

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8
Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress
Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress
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Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress

The Egyptian journal of medical human genetics, 2018-10, Vol.19 (4), p.321-324 [Peer Reviewed Journal]

2018 Ain Shams University ;2018. This work is published under https://creativecommons.org/licenses/by-nc-nd/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: 10.1016/j.ejmhg.2018.05.004

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9
Associations between smoking, components of metabolic syndrome and lipoprotein particle size
Associations between smoking, components of metabolic syndrome and lipoprotein particle size
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Associations between smoking, components of metabolic syndrome and lipoprotein particle size

BMC medicine, 2013-09, Vol.11 (1), p.195-195, Article 195 [Peer Reviewed Journal]

COPYRIGHT 2013 BioMed Central Ltd. ;COPYRIGHT 2013 South African Sports Medicine Association ;COPYRIGHT 2013 BioMed Central Ltd. ;2013 Slagter et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright © 2013 Slagter et al.; licensee BioMed Central Ltd. 2013 Slagter et al.; licensee BioMed Central Ltd. ;Wageningen University & Research ;ISSN: 1741-7015 ;ISSN: 1016-6742 ;EISSN: 1741-7015 ;EISSN: 2078-5143 ;DOI: 10.1186/1741-7015-11-195 ;PMID: 24228807

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10
Association of SLC30A8 rs13266634 gene polymorphism with type 2 diabetes mellitus (T2DM) in a population of Noakhali, Bangladesh: a case–control study
Association of SLC30A8 rs13266634 gene polymorphism with type 2 diabetes mellitus (T2DM) in a population of Noakhali, Bangladesh: a case–control study
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Association of SLC30A8 rs13266634 gene polymorphism with type 2 diabetes mellitus (T2DM) in a population of Noakhali, Bangladesh: a case–control study

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.22-11 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;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/s43042-024-00484-8

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11
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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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
Vitamin D levels and vitamin D receptor genetic variants in Egyptian cardiovascular disease patients with and without diabetes
Vitamin D levels and vitamin D receptor genetic variants in Egyptian cardiovascular disease patients with and without diabetes
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Vitamin D levels and vitamin D receptor genetic variants in Egyptian cardiovascular disease patients with and without diabetes

Egyptian Journal of Medical Human Genetics, 2021-06, Vol.22 (1), p.1-12 [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/s43042-021-00174-9

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14
Altered expression of long non-coding RNAs NRON and SNHG11 in patients with ischemic stroke
Altered expression of long non-coding RNAs NRON and SNHG11 in patients with ischemic stroke
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Altered expression of long non-coding RNAs NRON and SNHG11 in patients with ischemic stroke

Egyptian Journal of Medical Human Genetics, 2024-01, Vol.25 (1), p.11-8 [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/s43042-024-00482-w

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15
Gastro-esophageal and respiratory morbidity in children after esophageal atresia repair: a 23-year review from a single tertiary institution in Asia
Gastro-esophageal and respiratory morbidity in children after esophageal atresia repair: a 23-year review from a single tertiary institution in Asia
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Gastro-esophageal and respiratory morbidity in children after esophageal atresia repair: a 23-year review from a single tertiary institution in Asia

Annals of pediatric surgery, 2023-12, Vol.19 (1), p.19-11, Article 19 [Peer Reviewed Journal]

The Author(s) 2023 ;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: 2090-5394 ;ISSN: 1687-4137 ;EISSN: 2090-5394 ;DOI: 10.1186/s43159-023-00251-1

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16
Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis
Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis
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Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.84-9 [Peer Reviewed Journal]

The Author(s) 2023. corrected publication 2024 ;COPYRIGHT 2023 Springer ;The Author(s) 2023. corrected publication 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/s43042-023-00464-4

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17
Association of IL-4 (− 590 C/T) and IL-6 (− 174 G/C) gene polymorphism in South Indian CKD patients
Association of IL-4 (− 590 C/T) and IL-6 (− 174 G/C) gene polymorphism in South Indian CKD patients
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Association of IL-4 (− 590 C/T) and IL-6 (− 174 G/C) gene polymorphism in South Indian CKD patients

Egyptian Journal of Medical Human Genetics, 2024-02, Vol.25 (1), p.17-10 [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/s43042-024-00476-8

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18
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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19
Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls
Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls
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Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.29-7 [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/s43042-023-00408-y

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20
SIRT1 gene is associated with cardiovascular disease in the Iranian population
SIRT1 gene is associated with cardiovascular disease in the Iranian population
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SIRT1 gene is associated with cardiovascular disease in the Iranian population

The Egyptian journal of medical human genetics, 2015-04, Vol.16 (2), p.117-122 [Peer Reviewed Journal]

2014 ;Copyright Egyptian Society of Medical Human Genetics 2015 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2014.11.005

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