Ghada El-Kamah - Search Results

Year	Number of Results
2007	1
2009	2
2011	1
2013	1
2014	1
2016	2
2017	4
2018	1
2019	4
2020	4
2021	8
2022	6
2023	4
2024	1

1

Consanguinity and Inbreeding in Health and Disease in North African Populations.

Romdhane L, Mezzi N, Hamdi Y, El-Kamah G, Barakat A, Abdelhak S. Romdhane L, et al. Among authors: el kamah g. Annu Rev Genomics Hum Genet. 2019 Aug 31;20:155-179. doi: 10.1146/annurev-genom-083118-014954. Epub 2019 Apr 30. Annu Rev Genomics Hum Genet. 2019. PMID: 31039041 Review.

2

The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review.

Kumuthini J, Zick B, Balasopoulou A, Chalikiopoulou C, Dandara C, El-Kamah G, Findley L, Katsila T, Li R, Maceda EB, Monye H, Rada G, Thong MK, Wanigasekera T, Kennel H, Marimuthu V; G2MC Evidence investigators; Williams MS, Al-Mulla F, Abramowicz M. Kumuthini J, et al. Among authors: el kamah g. Hum Genet. 2022 Nov;141(11):1697-1704. doi: 10.1007/s00439-022-02452-x. Epub 2022 Apr 30. Hum Genet. 2022. PMID: 35488921 Free PMC article. Review.

3

Concise Review: Getting to the Core of Inherited Bone Marrow Failures.

Adam S, Melguizo Sanchis D, El-Kamah G, Samarasinghe S, Alharthi S, Armstrong L, Lako M. Adam S, et al. Among authors: el kamah g. Stem Cells. 2017 Feb;35(2):284-298. doi: 10.1002/stem.2543. Epub 2016 Dec 4. Stem Cells. 2017. PMID: 27870251 Free PMC article. Review.

4

Lenz-Majewski syndrome in a patient from Egypt.

Afifi HH, Abdel-Hamid MS, Mehrez MI, El-Kamah G, Abdel-Salam GMH. Afifi HH, et al. Among authors: el kamah g. Am J Med Genet A. 2019 Oct;179(10):2039-2042. doi: 10.1002/ajmg.a.61327. Epub 2019 Aug 12. Am J Med Genet A. 2019. PMID: 31403251

5

Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.

Abdel Megeid AK, Refeat MM, Ashaat EA, El-Kamah G, El-Saiedi SA, Elfalaki MM, El Ruby MO, Amr KS. Abdel Megeid AK, et al. Among authors: el kamah g. J Genet Eng Biotechnol. 2022 Aug 8;20(1):117. doi: 10.1186/s43141-022-00399-0. J Genet Eng Biotechnol. 2022. PMID: 35939165 Free PMC article.

6

Expanding the phenotypic spectrum and clinical severity associated with WLS gene.

Abdel-Salam GMH, Afifi HH, Abdel-Hamid MS, Ahmed NEB, Taher MB, El-Kamah G, Thiele H, Nürnberg PN, Bolz HJ. Abdel-Salam GMH, et al. Among authors: el kamah g. J Hum Genet. 2023 Sep;68(9):607-613. doi: 10.1038/s10038-023-01152-2. Epub 2023 Apr 28. J Hum Genet. 2023. PMID: 37106064

7

The African Society of Human Genetics successfully launches global data science workshops.

Nembaware V, Bennett D, Chimusa ER, Chikowore T, Daodu R, Bitoungui VN, Williams SM, Fatumo S, Healy S, Seoighe C, Wonkam A; African Society of Human Genetics. Nembaware V, et al. Trends Genet. 2023 Nov;39(11):803-807. doi: 10.1016/j.tig.2023.06.004. Epub 2023 Sep 14. Trends Genet. 2023. PMID: 37714735

8

Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.

Abdel Megeid AK, Refeat MM, Ashaat EA, El-Kamah G, El-Saiedi SA, Elfalaki MM, El Ruby MO, Amr KS. Abdel Megeid AK, et al. Among authors: el kamah g. J Genet Eng Biotechnol. 2022 Sep 21;20(1):137. doi: 10.1186/s43141-022-00420-6. J Genet Eng Biotechnol. 2022. PMID: 36129639 Free PMC article. No abstract available.

9

Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity.

Rabie EA, Sayed ISM, Amr K, Ahmed HA, Mostafa MI, Hassib NF, El-Sayed H, Zada SK, El-Kamah G. Rabie EA, et al. Among authors: el kamah g. Genes (Basel). 2022 Jun 13;13(6):1056. doi: 10.3390/genes13061056. Genes (Basel). 2022. PMID: 35741818 Free PMC article.

10

Defining the molecular pathology and consequent phenotypes in Egyptian HB patients.

El-Kamah GY, Mosaad RM, Taher MB, Amr KS. El-Kamah GY, et al. J Genet Eng Biotechnol. 2021 May 17;19(1):75. doi: 10.1186/s43141-021-00165-8. J Genet Eng Biotechnol. 2021. PMID: 33999344 Free PMC article.

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