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Year Number of Results
1982 1
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1994 3
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2007 9
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2011 2
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158 results

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Page 1
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss.
Oza AM, DiStefano MT, Hemphill SE, Cushman BJ, Grant AR, Siegert RK, Shen J, Chapin A, Boczek NJ, Schimmenti LA, Murry JB, Hasadsri L, Nara K, Kenna M, Booth KT, Azaiez H, Griffith A, Avraham KB, Kremer H, Rehm HL, Amr SS, Abou Tayoun AN; ClinGen Hearing Loss Clinical Domain Working Group. Oza AM, et al. Among authors: amr ss. Hum Mutat. 2018 Nov;39(11):1593-1613. doi: 10.1002/humu.23630. Hum Mutat. 2018. PMID: 30311386 Free PMC article.
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel.
Shen J, Oza AM, Del Castillo I, Duzkale H, Matsunaga T, Pandya A, Kang HP, Mar-Heyming R, Guha S, Moyer K, Lo C, Kenna M, Alexander JJ, Zhang Y, Hirsch Y, Luo M, Cao Y, Wai Choy K, Cheng YF, Avraham KB, Hu X, Garrido G, Moreno-Pelayo MA, Greinwald J, Zhang K, Zeng Y, Brownstein Z, Basel-Salmon L, Davidov B, Frydman M, Weiden T, Nagan N, Willis A, Hemphill SE, Grant AR, Siegert RK, DiStefano MT, Amr SS, Rehm HL, Abou Tayoun AN; ClinGen Hearing Loss Working Group. Shen J, et al. Among authors: amr ss. Genet Med. 2019 Nov;21(11):2442-2452. doi: 10.1038/s41436-019-0535-9. Epub 2019 Jun 4. Genet Med. 2019. PMID: 31160754 Free PMC article.
Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol.
Zhang Y, Dron JS, Bellows BK, Khera AV, Liu J, Balte PP, Oelsner EC, Amr SS, Lebo MS, Nagy A, Peloso GM, Natarajan P, Rotter JI, Willer C, Boerwinkle E, Ballantyne CM, Lutsey PL, Fornage M, Lloyd-Jones DM, Hou L, Psaty BM, Bis JC, Floyd JS, Vasan RS, Heard-Costa NL, Carson AP, Hall ME, Rich SS, Guo X, Kazi DS, de Ferranti SD, Moran AE. Zhang Y, et al. Among authors: amr ss. JAMA Cardiol. 2024 Mar 1;9(3):263-271. doi: 10.1001/jamacardio.2023.5366. JAMA Cardiol. 2024. PMID: 38294787 Free PMC article.
Jabir ibn Hayyan.
Amr SS, Tbakhi A. Amr SS, et al. Ann Saudi Med. 2007 Jan-Feb;27(1):53-4. doi: 10.4103/0256-4947.51533. Ann Saudi Med. 2007. PMID: 17337999 Free article. No abstract available.
Automated Pharmacogenomic Reports for Clinical Genome Sequencing.
Klanderman BJ, Koch C, Machini K, Parpattedar SS, Bandyadka S, Lin CF, Hynes E, Lebo MS, Amr SS. Klanderman BJ, et al. Among authors: amr ss. J Mol Diagn. 2022 Mar;24(3):205-218. doi: 10.1016/j.jmoldx.2021.12.001. Epub 2022 Jan 15. J Mol Diagn. 2022. PMID: 35041930 Free article.
Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease.
Zhang Y, Dron JS, Bellows BK, Khera AV, Liu J, Balte PP, Oelsner EC, Amr SS, Lebo MS, Nagy A, Peloso GM, Natarajan P, Rotter JI, Willer C, Boerwinkle E, Ballantyne CM, Lutsey PL, Fornage M, Lloyd-Jones DM, Hou L, Psaty BM, Bis JC, Floyd JS, Vasan RS, Heard-Costa NL, Carson AP, Hall ME, Rich SS, Guo X, Kazi DS, de Ferranti SD, Moran AE. Zhang Y, et al. Among authors: amr ss. Circulation. 2023 May 16;147(20):1556-1559. doi: 10.1161/CIRCULATIONAHA.123.064168. Epub 2023 May 15. Circulation. 2023. PMID: 37186683 Free PMC article. No abstract available.
Gastrointestinal stromal tumors. A clinicopathological study.
Alghamdi HM, Amr SS, Shawarby MA, Sheikh SS, Alsayyah AA, Alamri AM, Ismail MH, Almarhabi A, Alrefaee MA, Ahmed MI. Alghamdi HM, et al. Among authors: amr ss. Saudi Med J. 2019 Feb;40(2):126-130. doi: 10.15537/smj.2019.2.23913. Saudi Med J. 2019. PMID: 30723856 Free PMC article.
Massive Localized Lymphedema: Two Case Studies and Diagnostic Challenges.
Ba-Shammakh SA, Haj-Freej HM, Al-Naggar YS, Ghanem W, Haij MZ, Al-Mohd F, Hijazi E, Amr SS. Ba-Shammakh SA, et al. Among authors: amr ss. Cureus. 2023 Oct 16;15(10):e47092. doi: 10.7759/cureus.47092. eCollection 2023 Oct. Cureus. 2023. PMID: 38021692 Free PMC article.
Snakebites in Jordan: A clinical and epidemiological study.
Abu Baker MA, Al-Saraireh M, Amr Z, Amr SS, Warrell DA. Abu Baker MA, et al. Among authors: amr ss. Toxicon. 2022 Mar;208:18-30. doi: 10.1016/j.toxicon.2022.01.005. Epub 2022 Jan 10. Toxicon. 2022. PMID: 35026216
ME2 Deficiency Is Associated With Recessive Neurodevelopmental Disorder.
Almontashiri NAM, Alharby E, Saleh M, Abu-Farha M, Alasmari A, Gebbia M, Hiesl C, Peake RWA, Amr SS, Boles E, Roth FP, Abubaker J. Almontashiri NAM, et al. Among authors: amr ss. Clin Genet. 2025 Feb;107(2):201-207. doi: 10.1111/cge.14632. Epub 2024 Oct 14. Clin Genet. 2025. PMID: 39401966
158 results