Hussein IR - Search Results

1

Characterization of familial breast cancer in Saudi Arabia.

Merdad A, Gari MA, Hussein S, Al-Khayat S, Tashkandi H, Al-Maghrabi J, Al-Thubaiti F, Hussein IR, Koumosani T, Shaer N, Chaudhary AG, Abuzenadah AM, Al-Qahtani MH, Dallol A. Merdad A, et al. Among authors: hussein ir. BMC Genomics. 2015;16 Suppl 1(Suppl 1):S3. doi: 10.1186/1471-2164-16-S1-S3. Epub 2015 Jan 15. BMC Genomics. 2015. PMID: 25923920 Free PMC article.

2

Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015.

Shay JW, Homma N, Zhou R, Naseer MI, Chaudhary AG, Al-Qahtani M, Hirokawa N, Goudarzi M, Fornace AJ Jr, Baeesa S, Hussain D, Bangash M, Alghamdi F, Schulten HJ, Carracedo A, Khan I, Qashqari H, Madkhali N, Saka M, Saini KS, Jamal A, Al-Maghrabi J, Abuzenadah A, Chaudhary A, Al Qahtani M, Damanhouri G, Alkhatabi H, Goodeve A, Crookes L, Niksic N, Beauchamp N, Abuzenadah AM, Vaught J, Budowle B, Assidi M, Buhmeida A, Al-Maghrabi J, Buhmeida A, Assidi M, Merdad L, Kumar S, Miura S, Gomez K, Carracedo A, Rasool M, Rebai A, Karim S, Eldin HFN, Abusamra H, Alhathli EM, Salem N, Al-Qahtani MH, Kumar S, Faheem H, Agarwa A, Nieschlag E, Wistuba J, Damm OS, Beg MA, Abdel-Meguid TA, Mosli HA, Bajouh OS, Abuzenadah AM, Al-Qahtani MH, Coskun S, Abu-Elmagd M, Buhmeida A, Dallol A, Al-Maghrabi J, Hakamy S, Al-Qahtani W, Al-Harbi A, Hussain S, Assidi M, Al-Qahtani M, Abuzenadah A, Ozkosem B, DuBois R, Messaoudi SS, Dandana MT, Mahjoub T, Almawi WY, Abdalla S, Al-Aama MN, Elzawahry A, Takahashi T, Mimaki S, Furukawa E, Nakatsuka R, Kurosaka I, Nishigaki T, Nakamura H, Serada S, Naka T, Hirota S, Shibata T, Tsuchihara K, Nishida T, Kato M, Mehmood S, Ashraf NM, Asif A, Bilal M, Mehmood MS, Hussain … See abstract for full author list ➔ Shay JW, et al. Among authors: hussein ir. BMC Genomics. 2016 Jul 20;17 Suppl 6(Suppl 6):487. doi: 10.1186/s12864-016-2858-0. BMC Genomics. 2016. PMID: 27454254 Free PMC article.

3

Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams' syndrome patients in Saudi Arabia.

Hussein IR, Magbooli A, Huwait E, Chaudhary A, Bader R, Gari M, Ashgan F, Alquaiti M, Abuzenadah A, AlQahtani M. Hussein IR, et al. Mol Cytogenet. 2016 Aug 12;9:65. doi: 10.1186/s13039-016-0266-4. eCollection 2016. Mol Cytogenet. 2016. PMID: 27525043 Free PMC article.

4

Cellular mechanisms of osteoclast formation and lacunar resorption in giant cell granuloma of the jaw.

Itonaga I, Hussein I, Kudo O, Sabokbar A, Watt-Smith S, Ferguson D, Athanasou NA. Itonaga I, et al. J Oral Pathol Med. 2003 Apr;32(4):224-31. doi: 10.1034/j.1600-0714.2003.00069.x. J Oral Pathol Med. 2003. PMID: 12653862

5

Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability.

Karim S, Hussein IR, Schulten HJ, Alsaedi S, Mirza Z, Al-Qahtani M, Chaudhary A. Karim S, et al. Among authors: hussein ir. Children (Basel). 2023 Mar 31;10(4):662. doi: 10.3390/children10040662. Children (Basel). 2023. PMID: 37189911 Free PMC article.

6

Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.

Hussein IR, Bader RS, Chaudhary AG, Bassiouni R, Alquaiti M, Ashgan F, Schulten HJ, Al Qahtani MH. Hussein IR, et al. Pediatr Cardiol. 2018 Jun;39(5):924-940. doi: 10.1007/s00246-018-1842-7. Epub 2018 Mar 14. Pediatr Cardiol. 2018. PMID: 29541814

7

Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.

Chaudhary AG, Hussein IR, Abuzenadah A, Gari M, Bassiouni R, Sogaty S, Lary S, Al-Quaiti M, Al Balwi M, Al Qahtani M. Chaudhary AG, et al. Among authors: hussein ir. Pediatr Neurol. 2014 Apr;50(4):368-76. doi: 10.1016/j.pediatrneurol.2013.11.020. Epub 2013 Dec 4. Pediatr Neurol. 2014. PMID: 24630283

8

Association of angiotensin converting enzyme gene (I/D) polymorphism with hypertension and type 2 diabetes.

Zarouk WA, Hussein IR, Esmaeil NN, Raslan HM, Reheim HA, Moguib O, Emara NA, Aly AA, Hamed M. Zarouk WA, et al. Among authors: hussein ir. Bratisl Lek Listy. 2012;113(1):14-8. doi: 10.4149/bll_2012_003. Bratisl Lek Listy. 2012. PMID: 22380495

9

An SP1-binding site polymorphism in the COLIAI gene and osteoporosis in Egyptian patients with thalassemia major.

Hamed HM, Galal A, Ghamrawy ME, Abd El Azeem K, Hussein IR, Abd-Elgawad MF. Hamed HM, et al. Among authors: hussein ir. Blood Coagul Fibrinolysis. 2011 Mar;22(2):81-5. doi: 10.1097/MBC.0b013e32834248fb. Blood Coagul Fibrinolysis. 2011. PMID: 21178584

10

ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia.

Shammas C, Papasavva T, Felekis X, Christophorou C, Roomere H, Synodinos JT, Kanavakis E, El-Khateeb M, Hamamy H, Mahmoud T, Shboul M, El Beshlawy A, Filon D, Hussein IR, Galanello R, Romeo G, Kleanthous M. Shammas C, et al. Among authors: hussein ir. Clin Chem Lab Med. 2010 Dec;48(12):1713-8. doi: 10.1515/CCLM.2010.331. Epub 2010 Aug 13. Clin Chem Lab Med. 2010. PMID: 20704537

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