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Khaled Abu-Amero

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Geographic Areas

Saudi Arabia

Chemicals & Drugs

Physiology

Living Beings

Disorders

Procedures

Concepts & Ideas

Occupations

Population Genetics

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Co-Publications
Name
21
Bosley, Thomas
10
Dzimiri, Nduna
8
Hellani, Ali
6
Mohamed, Gamal
6
Al-Boudari, Olayan
5
Cabrera, Vicente
5
González, Ana
4
Larruga, José
4
Oystreck, Darren
4
Bohlega, Saeed
4
Wyngaard, Carol
4
Halablab, Mahmoud
3
Ozand, Pinar
3
Salih, Mustafa
3
Miles, Roger

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Publications

TOP 3
Hellani Ali; Al-Akoum Siham; Abu-Amero Khaled K
G6PD Mediterranean S188F codon mutation is common among Saudi sickle cell patients and increases the risk of stroke.
Abu-Amero K K; Milcarek B; Bosley T M
GSTM1 and GSTT1 deletion genotypes in various spontaneous optic neuropathies in Arabs.
Hellani Ali; Fadel Elias; El-Sadadi Shaker; El-Sweilam Hamdan; El-Dawood Ahmed; Abu-Amero Khaled K
Molecular spectrum of alpha-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia.

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All Publications

2009: Hellani Ali; Al-Akoum Siham; Abu-Amero Khaled K
G6PD Mediterranean S188F codon mutation is common among Saudi sickle cell patients and increases the risk of stroke.
Genetic testing and molecular biomarkers 2009;13(4):449-52.
2009: Abu-Amero K K; Milcarek B; Bosley T M
GSTM1 and GSTT1 deletion genotypes in various spontaneous optic neuropathies in Arabs.
The British journal of ophthalmology 2009;93(8):1101-4.
2009: Hellani Ali; Fadel Elias; El-Sadadi Shaker; El-Sweilam Hamdan; El-Dawood Ahmed; Abu-Amero Khaled K
Molecular spectrum of alpha-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia.
Genetic testing and molecular biomarkers 2009;13(2):219-21.
2009: Abu-Amero Khaled K; al Dhalaan Hesham; al Zayed Zayed; Hellani Ali; Bosley Thomas M
Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations.
Journal of the neurological sciences 2009;276(1-2):22-6.
2009: Hellani Ali; Almassri Nidal; Abu-Amero Khaled K
A novel mutation in the ADA gene causing severe combined immunodeficiency in an Arab patient: a case report.
Journal of medical case reports 2009;3():6799.
2009: Abu-Amero Khaled K; Hellani Ali; González Ana M; Larruga Jose M; Cabrera Vicente M; Underhill Peter A
Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions.
BMC genetics 2009;10():59.
2009: Abu-Amero Khaled K; Hellani Ali; Bender Patrick; Spaeth George L; Myers Jonathan; Katz L Jay; Moster Marlene; Bosley Thomas M
High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma.
Molecular vision 2009;15():1594-8.
2009: Ennafaa Hajer; Cabrera Vicente M; Abu-Amero Khaled K; González Ana M; Amor Mohamed B; Bouhaha Rym; Dzimiri Nduna; Elgaaïed Amel B; Larruga José M
Mitochondrial DNA haplogroup H structure in North Africa.
BMC genetics 2009;10():8.
2009: Hellani Ali; Baghdadi Hiba; Dabbour Nidal; Almassri Nidal; Abu-Amero Khaled K
A novel PTCH1 germline mutation distinguishes basal cell carcinoma from basaloid follicular hamartoma: a case report.
Journal of medical case reports 2009;3():52.
2008: Bosley Thomas M; Brodsky Michael C; Glasier Charles M; Abu-Amero Khaled K
Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.
Investigative ophthalmology & visual science 2008;49(12):5250-6.
2008: Sugiana Canny; Pagliarini David J; McKenzie Matthew; Kirby Denise M; Salemi Renato; Abu-Amero Khaled K; Dahl Hans-Henrik M; Hutchison Wendy M; Vascotto Katherine A; Smith Stacey M; Newbold Robert F; Christodoulou John; Calvo Sarah; Mootha Vamsi K; Ryan Michael T; Thorburn David R
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.
American journal of human genetics 2008;83(4):468-78.
2008: Abu-Amero Khaled K; Larruga Jose M; González Ana M; Bosley Thomas M
The role of mitochondrial haplogroups in non-arteritic anterior ischemic optic neuropathy.
Ophthalmic genetics 2008;29(3):111-6.
2008: Bohlega Saeed A; Abu-Amero Khaled K
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs.
Saudi medical journal 2008;29(7):952-6.
2008: Bosley Thomas M; Alorainy Ibrahim A; Salih Mustafa A; Aldhalaan Hesham M; Abu-Amero Khaled K; Oystreck Darren T; Tischfield Max A; Engle Elizabeth C; Erickson Robert P
The clinical spectrum of homozygous HOXA1 mutations.
American journal of medical genetics. Part A 2008;146A(10):1235-40.
2008: Al-Hassnan Zuhair N; Rashed Mohamed S; Al-Dirbashi Osama Y; Patay Zoltan; Rahbeeni Zuhair; Abu-Amero Khaled K
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with stroke-like imaging presentation: clinical, biochemical and molecular analysis.
Journal of the neurological sciences 2008;264(1-2):187-94.
2008: Abu-Amero Khaled K; Hellani Ali; Bohlega Saeed
Absence of mtDNA mutations in leukocytes of CADASIL patients.
BMC research notes 2008;1():16.
2008: Abu-Amero Khaled K; Morales Jose; Bosley Thomas M; Mohamed Gamal H; Cabrera Vicente M
The role of mitochondrial haplogroups in glaucoma: a study in an Arab population.
Molecular vision 2008;14():518-22.
2008: Abu-Amero Khaled K; Morales Jose; Mohamed Gamal H; Osman Mazen N; Bosley Thomas M
Glutathione S-transferase M1 and T1 polymorphisms in Arab glaucoma patients.
Molecular vision 2008;14():425-30.
2008: Abu-Amero Khaled K; Larruga José M; Cabrera Vicente M; González Ana M
Mitochondrial DNA structure in the Arabian Peninsula.
BMC evolutionary biology 2008;8():45.
2008: Abu-Amero Khaled K; Bosley Thomas M; Morales Jose
Analysis of nuclear and mitochondrial genes in patients with pseudoexfoliation glaucoma.
Molecular vision 2008;14():29-36.
2007: Abu-Amero Khaled K; Bosley Thomas M
Reassessment of the pathologic significance of the 9438 mitochondrial DNA mutation associated with LHON.
Ophthalmic genetics 2007;28(4):229-30.
2007: Abu-Amero Khaled K; Morales Jose; Osman Mazen N; Bosley Thomas M
Nuclear and mitochondrial analysis of patients with primary angle-closure glaucoma.
Investigative ophthalmology & visual science 2007;48(12):5591-6.
2007: Abu-Amero Khaled K; Bosley Thomas M
Mitochondrial DNA abnormalities in NAION.
The British journal of ophthalmology 2007;91(11):1561.
2007: Bosley T M; Salih M A; Alorainy I A; Oystreck D T; Nester M; Abu-Amero K K; Tischfield M A; Engle E C
Clinical characterization of the HOXA1 syndrome BSAS variant.
Neurology 2007;69(12):1245-53.
2007: Al-Dirbashi O Y; Abu-Amero K K; Alswaid A F; Hoffmann G F; Al-Qahtani K; Rashed M S
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 gene.
Journal of inherited metabolic disease 2007;30(4):611.
2007: Bohlega Saeed; Al Shubili Asmahan; Edris Abdulrahman; Alreshaid Abdulrahman; Alkhairallah Thamer; AlSous M Walid; Farah Samir; Abu-Amero Khaled K
CADASIL in Arabs: clinical and genetic findings.
BMC medical genetics 2007;8():67.
2007: Bosley Thomas M; Constantinescu Cris S; Tench Christopher R; Abu-Amero Khaled K
Mitochondrial changes in leukocytes of patients with optic neuritis.
Molecular vision 2007;13():1516-28.
2007: González Ana M; Larruga José M; Abu-Amero Khaled K; Shi Yufei; Pestano José; Cabrera Vicente M
Mitochondrial lineage M1 traces an early human backflow to Africa.
BMC genomics 2007;8():223.
2007: Abu-Amero Khaled K; Al-Mohanna Futwan; Al-Boudari Olayan M; Mohamed Gamal H; Dzimiri Nduna
The interactive role of type 2 diabetes mellitus and E-selectin S128R mutation on susceptibility to coronary heart disease.
BMC medical genetics 2007;8():35.
2007: Abu-Amero Khaled K; González Ana M; Larruga Jose M; Bosley Thomas M; Cabrera Vicente M
Eurasian and African mitochondrial DNA influences in the Saudi Arabian population.
BMC evolutionary biology 2007;7():32.
2006: Abu-Amero Khaled K; Ozand Pinar T; Al-Dhalaan Hesham
Novel mitochondrial DNA transversion mutation in transfer ribonucleic acid for leucine 2 (CUN) in a patient with the clinical features of MELAS.
Journal of child neurology 2006;21(11):971-2.
2006: Abu-Amero Khaled K; Bosley Thomas M
Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
Investigative ophthalmology & visual science 2006;47(10):4211-20.
2006: Bosley Thomas M; Oystreck Darren T; Robertson Richard L; al Awad Abdulaziz; Abu-Amero Khaled; Engle Elizabeth C
Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A.
Brain : a journal of neurology 2006;129(Pt 9):2363-74.
2006: Abu-Amero K K; Bosley T M
Increased relative mitochondrial DNA content in leucocytes of patients with NAION.
The British journal of ophthalmology 2006;90(7):823-5.
2006: Abu-Amero Khaled K; Morales Jose; Bosley Thomas M
Mitochondrial abnormalities in patients with primary open-angle glaucoma.
Investigative ophthalmology & visual science 2006;47(6):2533-41.
2006: Abu-Amero K K; Owaidah T M; Al-Mahed M
Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.
Journal of thrombosis and haemostasis : JTH 2006;4(5):1152-3.
2006: Abu-Amero K K; Alzahrani A S; Zou M; Shi Y
Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome.
Oncogene 2006;25(5):677-84.
2006: Abu-Amero K K; Bosley T M
Prothrombotic and atherosclerotic risk factors lack significance in NAION patients harbouring mitochondrial DNA mutations.
The British journal of ophthalmology 2006;90(1):119-20.
2006: Abu-Amero Khaled K; Al-Boudari Olayan M; Mohamed Gamal H; Dzimiri Nduna
E-selectin S128R polymorphism and severe coronary artery disease in Arabs.
BMC medical genetics 2006;7():52.
2006: Abu-Amero Khaled K; Al-Boudari Olayan M; Mohamed Gamal H; Dzimiri Nduna
T null and M null genotypes of the glutathione S-transferase gene are risk factor for CAD independent of smoking.
BMC medical genetics 2006;7():38.
2006: Abu-Amero Khaled K; Al-Boudari Olayan M; Mohamed Gamal H; Dzimiri Nduna
The Glu27 genotypes of the beta2-adrenergic receptor are predictors for severe coronary artery disease.
BMC medical genetics 2006;7():31.
2005: Abu-Amero Khaled K; Al-Boudari Olayan M; Mohamed Gamal H; Dzimiri Nduna
Beta 3 adrenergic receptor Trp64Arg polymorphism and manifestation of coronary artery disease in Arabs.
Human biology; an international record of research 2005;77(6):795-802.
2005: Abu-Amero Khaled K; Bosley Thomas M
Detection of mitochondrial respiratory dysfunction in circulating lymphocytes using resazurin.
Archives of pathology & laboratory medicine 2005;129(10):1295-8.
2005: Abu-Amero K K; Bosley T M; Bohlega S; McLean D
Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation.
The British journal of ophthalmology 2005;89(10):1380-1.
2005: Abu-Amero K K; Miles R J; Halablab M A
Cholesterol protects Acholeplasma laidlawii against oxidative damage caused by hydrogen peroxide.
Veterinary research communications 2005;29(5):373-80.
2005: Bosley T M; Salih M A M; Jen J C; Lin D D M; Oystreck D; Abu-Amero K K; MacDonald D B; al Zayed Z; al Dhalaan H; Kansu T; Stigsby B; Baloh R W
Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3.
Neurology 2005;64(7):1196-203.
2005: Abu-Amero Khaled K; Bosley Thomas M; Bohlega Saeed; Hansen Erik
Mitochondrial T9957C mutation in association with NAION and seizures but not MELAS.
Ophthalmic genetics 2005;26(1):31-6.
2005: Abu-Amero Khaled K; Alzahrani Ali S; Zou Minjing; Shi Yufei
High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines.
Oncogene 2005;24(8):1455-60.
2004: Abu-Amero K; Zou M; Shi Y
Mitochondrial A135149 mutation without MELAS but in association with papillary thyroid carcinoma.
Clinical genetics 2004;66(6):569-70.
2004: Bosley Thomas M; Abu-Amero Khaled K; Ozand Pinar T
Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy.
Neurology 2004;63(7):1305-8.
2004: Abu-Amero Khaled K; Owaidah Tarek M; Al Jefri Abduallah; Al-Ghonaium Abdulaziz; Fawaz Ibrahim M; Al-Hamed Mohammed H
A novel splice site mutation in the WAS gene causes Wiskott-Aldrich syndrome in two siblings of a Saudi family.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(7):599-603.
2004: Abu-Amero K K; Halablab M A
Evaluation of the COBAS AMPLICOR MTB test for the detection of Mycobacterium tuberculosis complex.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-?i??iyah li-sharq al-mutawassi? 2004;10(3):329-35.
2004: Abu-Amero Khaled K; Wyngaard Carol A; Dzimiri Nduna
Association of the platelet glycoprotein receptor IIIa (PlA1/PlA1) genotype with coronary artery disease in Arabs.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(1):77-9.
2003: Al-Odaib Ali N; Abu-Amero Khaled K; Ozand Pinar T; Al-Hellani Ali M
A new era for preventive genetic programs in the Arabian Peninsula.
Saudi medical journal 2003;24(11):1168-75.
2003: Abu-Amero Khaled K; Wyngaard Carol A; Dzimiri Nduna
Prevalence and role of methylenetetrahydrofolate reductase 677 C-->T and 1298 A-->C polymorphisms in coronary artery disease in Arabs.
Archives of pathology & laboratory medicine 2003;127(10):1349-52.
2003: Abu-Amero Khaled
Human genetics information on the Web.
The journal of the Royal Society for the Promotion of Health 2003;123(2):102-4.
2003: Abu-Amero Khaled K; Wyngaard Carol A; Al-Boudari Olyan M; Kambouris Marios; Dzimiri Nduna
Lack of association of lipoprotein lipase gene polymorphisms with coronary artery disease in the Saudi Arab population.
Archives of pathology & laboratory medicine 2003;127(5):597-600.
2003: Abu-Amero Khaled K; Al-Hamed Mohammed H; Al-Batniji Fatma S
Homozygous protein C deficiency with purpura fulminans: report of a new case and a description of a novel mutation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2003;14(3):303-6.
2002: Abu-Amero Khaled K; Wyngaard Carol A; Kambouris Marios; Dzimiri Nduna
Prevalence of the 20210 G-->A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population.
Archives of pathology & laboratory medicine 2002;126(9):1087-90.
2002: Abu-Amero K K
Status of antituberculosis drug resistance in Saudi Arabia 1979-98.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-?i??iyah li-sharq al-mutawassi? 2002;8(4-5):664-70.
2002: Abu-Amero K K
Overview of the laboratory accreditation programme of the College of American Pathologists.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-?i??iyah li-sharq al-mutawassi? 2002;8(4-5):654-63.
2002: Abu-Amero K
Tuberculosis information on the Web.
The journal of the Royal Society for the Promotion of Health 2002;122(2):82-5.
2002: Abu-Amero Khaled K
Review of the current status of drug-resistant tuberculosis in Saudi Arabia.
Annals of Saudi medicine 2002;22(3-4):236-8.
2002: Abu-Amero K K; Halablab M A; Miles R J
Alternative to fluorescence assays to monitor fusion between Acholeplasma laidlawii cells and liposomes.
Letters in applied microbiology 2002;35(6):528-32.
2000: Abu-Amero K K; Abu-Groun E A; Halablab M A; Miles R J
Kinetics and distribution of alcohol oxidising activity in Acholeplasma and Mycoplasma species.
FEMS microbiology letters 2000;183(1):147-51.

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