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Ali Al Odaib

Research Profile

Geographic Areas

Saudi Arabia

Physiology

Concepts & Ideas

Consanguinity

Procedures

Disorders

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Devices

Oligonucleotide Array Sequence Analysis

Chemicals & Drugs

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Publications

TOP 3
Namik Kaya; Sahar Tulbah; Mohammed Al-Amoudi; Albandary Al-Bakheet; Fuad Al-Mutairi; Ali N Al Odaib; Banan Al-Younes; Dilek Colak; Maha Daghestani; Aida I Al Aqeel
Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia.
M Al-Owain; H Bamashmous; A Edrees; Eissa Faqeih; W Garout; Faiqa Imtiaz; B Meyer; Zuhair Rahbeeni; Mohamed S Rashed; Nadia A Sakati; T Shuaib; S Al-Ameer; Mohammed Al-Amoudi; A Al-Hashem; Zuhair N Al-Hassnan; Ali N Al Odaib; J Y Al-Aama
Smith-Lemli-Opitz syndrome among Arabs.
I A Almaghlouth; Ali N Al Odaib; J Y Mohamed; Lujane Y Al-Ahaidib; Mohammed Al-Amoudi; Fowzan S Alkuraya
5-Oxoprolinase deficiency: report of the first human OPLAH mutation.

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All Publications

2013: Namik Kaya; Sahar Tulbah; Mohammed Al-Amoudi; Albandary Al-Bakheet; Fuad Al-Mutairi; Ali N Al Odaib; Banan Al-Younes; Dilek Colak; Maha Daghestani; Aida I Al Aqeel
Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia.
Gene 2013;513(2):297-300.
2012: M Al-Owain; H Bamashmous; A Edrees; Eissa Faqeih; W Garout; Faiqa Imtiaz; B Meyer; Zuhair Rahbeeni; Mohamed S Rashed; Nadia A Sakati; T Shuaib; S Al-Ameer; Mohammed Al-Amoudi; A Al-Hashem; Zuhair N Al-Hassnan; Ali N Al Odaib; J Y Al-Aama
Smith-Lemli-Opitz syndrome among Arabs.
Clinical genetics 2012;82(2):165-72.
2012: I A Almaghlouth; Ali N Al Odaib; J Y Mohamed; Lujane Y Al-Ahaidib; Mohammed Al-Amoudi; Fowzan S Alkuraya
5-Oxoprolinase deficiency: report of the first human OPLAH mutation.
Clinical genetics 2012;82(2):193-6.
2012: Namik Kaya; Inci V Kayaalp; Nahit M Mukaddes; Michael J Nester; Nadia A Sakati; Nada Abu-Dheim; Albandary Albakheet; Hesham Al-Dhalaan; Mohammad Al-Dosari; Naji Al-Dosari; Zuhair N Al-Hassnan; Fowzan S Alkuraya; Ali N Al Odaib; Mohammad Al-Owain; Moeenaldeen Al-Sayed; Banan Al-Younes; Jawaher Al-Zahrani; Aziza Chedrawi; Dilek Colak; Aysin Dervent; Generaso G Gascon; Hulya Gunoz; Bedri Karakas; Pinar T Ozand
A novel X-linked disorder with developmental delay and autistic features.
Annals of neurology 2012;71(4):498-508.
2012: Maha H Daghestani; Mazin H Daghestani; Abdelmoneim Eldali; Nadia A Al-Eisa; Ali N Al Odaib; Sawsan A. Omer; Arjumand Warsy; Zeinab K Hassan
Arginine 16 Glycine Polymorphism in β2-Adrenergic Receptor Gene is Associated with Obesity, Hyperlipidemia, Hyperleptinemia, and Insulin Resistance in Saudis.
International journal of endocrinology 2012;2012():945608.
2011: Jawaher Al-Zahrani; Naji Al-Dosari; Nada Abudheim; Tarfa A Alshidi; Dilek Colak; Ola Al-Habit; Ali N Al Odaib; Nadia A Sakati; Brian Meyer; Pinar T Ozand; Namik Kaya
Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects.
Molecular cytogenetics 2011;4():9.
2011: Dilek Colak; Hesham Al-Dhalaan; Michael Nester; Albandary Albakheet; Banan Al-Younes; Zuhair N Al-Hassnan; Mohammad Al-Dosari; Aziza Chedrawi; Muhammad Al-Owain; Nada Abudheim; Laila Al-Alwan; Ali N Al Odaib; Pinar Ozand; Mehmet Sait Inan; Namik Kaya
Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways.
Genomics 2011;97(1):19-28.
2010: Maha H Daghestani; Arjumand S Warsy; Mazin H Daghestani; Ali N Al Odaib; Abdelmoneim Eldali; Nadia A Al-Eisa; Sabah Al-zhrani
The Gln27Glu polymorphism in β2-adrenergic receptor gene is linked to hypertriglyceridemia, hyperinsulinemia and hyperleptinemia in Saudis.
Lipids in health and disease 2010;9():90.
2008: Namik Kaya; Mohammad Al-Owain; Albandary Albakheet; Dilek Colak; Ali N Al Odaib; Faiqa Imtiaz; Serdar Coskun; Moeenaldeen Al-Sayed; Zuhair N Al-Hassnan; Hamad Al-Zaidan; Brian Meyer; Pinar T Ozand
Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia.
European journal of medical genetics 2008;51(6):558-65.
2008: Namik Kaya; Faiqa Imtiaz; Dilek Colak; Moeenaldeen Al-Sayed; Ali N Al Odaib; Fatma Al-Zahrani; Bashayer R Al-Mubarak; Mohammad Al-Owain; Hesham Al-Dhalaan; Aziza Chedrawi; Zuhair N Al-Hassnan; Serdar Coskun; Nadia A Sakati; Pinar T Ozand; Brian F Meyer
Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(9):675-84.
2007: Maha H Daghestani; Pinar T Ozand; Ahmed R Al-Himadi; Ali N Al Odaib
Hormonal levels of leptin, insulin, ghrelin, and neuropeptide Y in lean, overweight, and obese Saudi females.
Saudi medical journal 2007;28(8):1191-7.
2006: Ali N Al Odaib; Mohamed S Rashed; Theodore Page; William L Nyhan; Pinar T Ozand
3-Methylcrotonyl-CoA carboxylase deficiency. A long-term outcome.
Saudi medical journal 2006;27(5):732-3.
2006: Osama Y Al-Dirbashi; Nafiz Oncu Can; Ali N Al Odaib; Minnie Jacob; Mohamed S Rashed
Rapid liquid chromatography-tandem mass spectrometry method for quantification of ziprasidone in human plasma.
Biomedical chromatography : BMC 2006;20(4):365-8.
2006: Essam Al Shail; Ali N Al Odaib; Pinar T Ozand
Early neurosurgical intervention in spondyloepiphyseal dysplasias.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2006;22(3):249-52.
2005: Osama Y Al-Dirbashi; Minnie Jacob; Mohammed Al-Amoudi; Khalid Al-Kahtani; Ali N Al Odaib; Fahad El-Badaoui; Mohamed S Rashed
Quantification of glutaric and 3-hydroxyglutaric acids in urine of glutaric acidemia type I patients by HPLC with intramolecular excimer-forming fluorescence derivatization.
Clinica chimica acta; international journal of clinical chemistry 2005;359(1-2):179-88.
2004: Ali Hellani; Edward H Schuchman; Ali N Al Odaib; Aida Al Aqueel; Kamal Jaroudi; Pinar T Ozand; Serdar Coskun
Preimplantation genetic diagnosis for Niemann-Pick disease type B.
Prenatal diagnosis 2004;24(12):943-8.
2004: Ali Hellani; Serdar Coskun; Moncef Benkhalifa; Abdelghani Tbakhi; Nadia A Sakati; Ali N Al Odaib; Pinar T Ozand
Multiple displacement amplification on single cell and possible PGD applications.
Molecular human reproduction 2004;10(11):847-52.
2003: Ali N Al Odaib; Khaled K Abu-Amero; Pinar T Ozand; Ali M Al-Hellani
A new era for preventive genetic programs in the Arabian Peninsula.
Saudi medical journal 2003;24(11):1168-75.
2003: Jalaluddin Bhuiyan; Ali N Al Odaib; Pinar T Ozand
A simple, rapid test for the differential diagnosis of glycogen storage disease type 3.
Clinica chimica acta; international journal of clinical chemistry 2003;335(1-2):21-6.