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Page 1
Poly(ADP-Ribose) Polymerases in Aging - Friend or Foe?
Vida A, Abdul-Rahman O, Mikó E, Brunyánszki A, Bai P. Vida A, et al. Curr Protein Pept Sci. 2016;17(7):705-712. doi: 10.2174/1389203717666160419144959. Curr Protein Pept Sci. 2016. PMID: 27090903 Review.
AMP-Activated Kinase (AMPK) Activation by AICAR in Human White Adipocytes Derived from Pericardial White Adipose Tissue Stem Cells Induces a Partial Beige-Like Phenotype.
Abdul-Rahman O, Kristóf E, Doan-Xuan QM, Vida A, Nagy L, Horváth A, Simon J, Maros T, Szentkirályi I, Palotás L, Debreceni T, Csizmadia P, Szerafin T, Fodor T, Szántó M, Tóth A, Kiss B, Bacsó Z, Bai P. Abdul-Rahman O, et al. PLoS One. 2016 Jun 20;11(6):e0157644. doi: 10.1371/journal.pone.0157644. eCollection 2016. PLoS One. 2016. PMID: 27322180 Free PMC article.
Olaparib induces browning of in vitro cultures of human primary white adipocytes.
Nagy L, Rauch B, Balla N, Ujlaki G, Kis G, Abdul-Rahman O, Kristóf E, Sipos A, Antal M, Tóth A, Debreceni T, Horváth A, Maros T, Csizmadia P, Szerafin T, Bai P. Nagy L, et al. Biochem Pharmacol. 2019 Sep;167:76-85. doi: 10.1016/j.bcp.2019.06.022. Epub 2019 Jun 26. Biochem Pharmacol. 2019. PMID: 31251940
Maternal and paternal risk factors for fetal alcohol spectrum disorders: Alcohol and other drug use as proximal influences.
May PA, Hasken JM, de Vries MM, Marais AS, Abdul-Rahman O, Robinson LK, Adam MP, Manning MA, Kalberg WO, Buckley D, Seedat S, Parry CDH, Hoyme HE. May PA, et al. Among authors: abdul rahman o. Alcohol Clin Exp Res (Hoboken). 2023 Nov;47(11):2090-2109. doi: 10.1111/acer.15193. Epub 2023 Oct 4. Alcohol Clin Exp Res (Hoboken). 2023. PMID: 38226752
Maternal risk factors for fetal alcohol spectrum disorders: Distal variables.
May PA, Hasken JM, de Vries MM, Marais AS, Abdul-Rahman O, Robinson LK, Adam MP, Manning MA, Kalberg WO, Buckley D, Snell CL, Seedat S, Parry CDH, Hoyme HE. May PA, et al. Among authors: abdul rahman o. Alcohol Clin Exp Res (Hoboken). 2024 Feb;48(2):319-344. doi: 10.1111/acer.15246. Epub 2024 Jan 8. Alcohol Clin Exp Res (Hoboken). 2024. PMID: 38105110
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Kaur M, Blair J, Devkota B, Fortunato S, Clark D, Lawrence A, Kim J, Do W, Semeo B, Katz O, Mehta D, Yamamoto N, Schindler E, Al Rawi Z, Wallace N, Wilde JJ, McCallum J, Liu J, Xu D, Jackson M, Rentas S, Tayoun AA, Zhe Z, Abdul-Rahman O, Allen B, Angula MA, Anyane-Yeboa K, Argente J, Arn PH, Armstrong L, Basel-Salmon L, Baynam G, Bird LM, Bruegger D, Ch'ng GS, Chitayat D, Clark R, Cox GF, Dave U, DeBaere E, Field M, Graham JM Jr, Gripp KW, Greenstein R, Gupta N, Heidenreich R, Hoffman J, Hopkin RJ, Jones KL, Jones MC, Kariminejad A, Kogan J, Lace B, Leroy J, Lynch SA, McDonald M, Meagher K, Mendelsohn N, Micule I, Moeschler J, Nampoothiri S, Ohashi K, Powell CM, Ramanathan S, Raskin S, Roeder E, Rio M, Rope AF, Sangha K, Scheuerle AE, Schneider A, Shalev S, Siu V, Smith R, Stevens C, Tkemaladze T, Toimie J, Toriello H, Turner A, Wheeler PG, White SM, Young T, Loomes KM, Pipan M, Harrington AT, Zackai E, Rajagopalan R, Conlin L, Deardorff MA, McEldrew D, Pie J, Ramos F, Musio A, Kline AD, Izumi K, Raible SE, Krantz ID. Kaur M, et al. Among authors: abdul rahman o. Am J Med Genet A. 2023 Aug;191(8):2113-2131. doi: 10.1002/ajmg.a.63247. Epub 2023 Jun 28. Am J Med Genet A. 2023. PMID: 37377026
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
Rots D, Jakub TE, Keung C, Jackson A, Banka S, Pfundt R, de Vries BBA, van Jaarsveld RH, Hopman SMJ, van Binsbergen E, Valenzuela I, Hempel M, Bierhals T, Kortüm F, Lecoquierre F, Goldenberg A, Hertz JM, Andersen CB, Kibæk M, Prijoles EJ, Stevenson RE, Everman DB, Patterson WG, Meng L, Gijavanekar C, De Dios K, Lakhani S, Levy T, Wagner M, Wieczorek D, Benke PJ, Lopez Garcia MS, Perrier R, Sousa SB, Almeida PM, Simões MJ, Isidor B, Deb W, Schmanski AA, Abdul-Rahman O, Philippe C, Bruel AL, Faivre L, Vitobello A, Thauvin C, Smits JJ, Garavelli L, Caraffi SG, Peluso F, Davis-Keppen L, Platt D, Royer E, Leeuwen L, Sinnema M, Stegmann APA, Stumpel CTRM, Tiller GE, Bosch DGM, Potgieter ST, Joss S, Splitt M, Holden S, Prapa M, Foulds N, Douzgou S, Puura K, Waltes R, Chiocchetti AG, Freitag CM, Satterstrom FK, De Rubeis S, Buxbaum J, Gelb BD, Branko A, Kushima I, Howe J, Scherer SW, Arado A, Baldo C, Patat O, Bénédicte D, Lopergolo D, Santorelli FM, Haack TB, Dufke A, Bertrand M, Falb RJ, Rieß A, Krieg P, Spranger S, Bedeschi MF, Iascone M, Josephi-Taylor S, Roscioli T, Buckley MF, Liebelt J, Dagli AI, Aten E, Hurst ACE, Hicks A, Suri M, Aliu E, Naik S, Sidlow R, Coursimault J, Ni… See abstract for full author list ➔ Rots D, et al. Among authors: abdul rahman o. Am J Hum Genet. 2023 Jun 1;110(6):963-978. doi: 10.1016/j.ajhg.2023.04.008. Epub 2023 May 16. Am J Hum Genet. 2023. PMID: 37196654 Free PMC article.
The prevalence of fetal alcohol spectrum disorders in rural communities in South Africa: A third regional sample of child characteristics and maternal risk factors.
May PA, de Vries MM, Marais AS, Kalberg WO, Buckley D, Hasken JM, Abdul-Rahman O, Robinson LK, Manning MA, Seedat S, Parry CDH, Hoyme HE. May PA, et al. Among authors: abdul rahman o. Alcohol Clin Exp Res. 2022 Oct;46(10):1819-1836. doi: 10.1111/acer.14922. Epub 2022 Sep 1. Alcohol Clin Exp Res. 2022. PMID: 35971629 Free PMC article.
93 results