FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Muhammad Faiyaz-Ul-Haque

Research Profile

Concepts & Ideas

Genes & Molecular Sequences

Recessive Genes

Procedures

Physiology

Geographic Areas

Disorders

Chemicals & Drugs

Living Beings

Homozygote

Co-author Network

Publications

TOP 3
S H E Zaidi; Halah Abalkhail; A Al-Abdullatif; Zuhair N Al-Hassnan; A Balobaid; Muhammad Faiyaz-Ul-Haque; I Peltekova; Zuhair Rahbeeni; T Shuaib; M Al-Owain
Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria.
Mahesh Kappanayil; Krishna Kumar; Renu Kurup; Fransiska Malfait; Swapna Menon; Sheela Nampoothiri; Hiran K Ravindran; Marjolijn Renard; Paul Coucke; Muhammad Faiyaz-Ul-Haque; Rajesh Kannan; Anne De Paepe
Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis.
Bassam S Bin-Abbas; Muhammad Faiyaz-Ul-Haque; Abdullah H Al-Fares; Sulaiman S Al-Gazlan; Jalaluddin A Bhuiyan; Saleh Z Al-Muhsen
Autoimmune polyglandular syndrome type 1 in Saudi children.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Muhammad Faiyaz-Ul-Haque (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: S H E Zaidi; Halah Abalkhail; A Al-Abdullatif; Zuhair N Al-Hassnan; A Balobaid; Muhammad Faiyaz-Ul-Haque; I Peltekova; Zuhair Rahbeeni; T Shuaib; M Al-Owain
Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria.
Clinical genetics 2012;81(6):563-70.
2012: Mahesh Kappanayil; Krishna Kumar; Renu Kurup; Fransiska Malfait; Swapna Menon; Sheela Nampoothiri; Hiran K Ravindran; Marjolijn Renard; Paul Coucke; Muhammad Faiyaz-Ul-Haque; Rajesh Kannan; Anne De Paepe
Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis.
Orphanet journal of rare diseases 2012;7():61.
2010: Bassam S Bin-Abbas; Muhammad Faiyaz-Ul-Haque; Abdullah H Al-Fares; Sulaiman S Al-Gazlan; Jalaluddin A Bhuiyan; Saleh Z Al-Muhsen
Autoimmune polyglandular syndrome type 1 in Saudi children.
Saudi medical journal 2010;31(7):788-92.
2010: Muhammad Faiyaz-Ul-Haque; Syed Zaidi; R M Hasanato; A Al-Abdullatif; A Cluntun; G Teresita; M Toulimat; R Al-Nounou; Fouad Al Dayel; I Peltekova; J A K M Bhuiyan
Genetics of glucose-6-phosphate dehydrogenase deficiency in Saudi patients.
Clinical genetics 2010;78(1):98-100.
2010: Muhammad Faiyaz-Ul-Haque; Abdullah Al-Jefri; Fouad Al Dayel; Jalaluddin A K M Bhuiyan; Hala A Abalkhail; Randa Al-Nounou; Ahmed Al-Abdullatif; Monogaran S Pulicat; Ameera Gaafar; Ayodele A Alaiya; Iskra Peltekova; Syed Zaidi
A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations.
European journal of pediatrics 2010;169(6):661-6.
2010: Ali S Alzahrani; Omalkhaire Alshaikh; Muhammad Faiyaz-Ul-Haque; Halah Abalkhail; Fouad Al Dayel; Hindi Al Hindi
Multiple paraganglioma syndrome type 4 due to succinate dehydrogenase B mutation: diagnostic and therapeutic challenges of a skull base paraganglioma masquerading as nasopharyngeal cancer.
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2010;16(3):452-8.
2010: Muhammad Faiyaz-Ul-Haque; Sulaiman Al-Gazlan; Halah A Abalkhail; Ahmad Al-Abdulatif; Mohamed Toulimat; Iskra Peltekova; Agha M R Khaliq; Fouad Al Dayel; Syed Zaidi
Novel and recurrent mutations in the C1NH gene of Arab patients affected with hereditary angioedema.
International archives of allergy and immunology 2010;151(2):149-54.
2009: Muhammad Faiyaz-Ul-Haque; A Al-Jefri; H A Abalkhail; M Toulimat; M A Al-Muallimi; M S Pulicat; Ameera Gaafar; A A Alaiya; F Al-Dayel; I Peltekova; Syed Zaidi
A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease).
Clinical genetics 2009;76(6):569-72.
2009: Muhammad Faiyaz-Ul-Haque; Mohammed Al-Owain; Fouad Al Dayel; Zuhair N Al-Hassnan; Hamad Al-Zaidan; Zuhair Rahbeeni; Moeenaldeen Al-Sayed; Ameera Balobaid; Ahmad Cluntun; Mohamed Toulimat; Hala Abalkhail; Iskra Peltekova; Syed Zaidi
Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency.
European journal of pediatrics 2009;168(12):1467-71.
2009: Muhammad Faiyaz-Ul-Haque; B Bin-Abbas; A Al-Abdullatif; H Abdullah Abalkhail; M Toulimat; S Al-Gazlan; A M Almutawa; A Al-Sagheir; I Peltekova; F Al-Dayel; Syed Zaidi
Novel and recurrent mutations in the AIRE gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients.
Clinical genetics 2009;76(5):431-40.
2009: Syed Zaidi; S Meyer; Vanya D Peltekova; Angelika Lindinger; Ahmad S Teebi; Muhammad Faiyaz-Ul-Haque
A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin.
European journal of pediatrics 2009;168(7):867-70.
2009: Muhammad Faiyaz-Ul-Haque; Syed Zaidi; Nouriyah Al-Sanna; Abdulrahman Alswaid; Tariq Momenah; Namik Kaya; Fouad Al Dayel; Issam Bouhoaigah; Mohammed Saliem; Lap-Chee Tsui; Ahmad S Teebi
A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome.
Atherosclerosis 2009;203(2):466-71.
2008: Aziza K Chedrawi; Ayman Ali; Zuhair N Al-Hassnan; Muhammad Faiyaz-Ul-Haque; Barry Wolf
Profound biotinidase deficiency in a child with predominantly spinal cord disease.
Journal of child neurology 2008;23(9):1043-8.
2008: Muhammad Faiyaz-Ul-Haque; Eissa A Faqeih; Hamad Al-Zaidan; Amal Al-Shammary; Syed Zaidi
Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5.
Journal of bone and mineral metabolism 2008;26(6):648-52.
2007: Muhammad Faiyaz-Ul-Haque; Syed Zaidi; M S Al-Mureikhi; I Peltekova; Lap-Chee Tsui; Ahmad S Teebi
Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar.
Clinical genetics 2007;72(2):164-6.
2006: Daniela G Seidler; Muhammad Faiyaz-Ul-Haque; Uwe Hansen; George W Yip; Syed Zaidi; Ahmad S Teebi; Ludwig Kiesel; Martin Götte
Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers-Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (beta4GalT-7).
Journal of molecular medicine (Berlin, Germany) 2006;84(7):583-94.
2005: Syed Zaidi; V Peltekova; S Meyer; Angelika Lindinger; A D Paterson; Lap-Chee Tsui; Muhammad Faiyaz-Ul-Haque; Ahmad S Teebi
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13.
Clinical genetics 2005;67(2):183-8.
2005: Muhammad Arshad Rafiq; Muhammad Faiyaz-Ul-Haque; Mohammad Amin Ud Din; Sajid Malik; Muhammad Sohail; Maqsood Anwar; Sayedul Haque; Andrew D Paterson; Lap-Chee Tsui; Wasim Ahmad
A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1.
The Journal of investigative dermatology 2005;124(2):338-42.
2005: S Meyer; Muhammad Faiyaz-Ul-Haque; M Zankl; N-L Sailer; N Marx; HG Limbach; Angelika Lindinger
[Arterial tortuosity syndrome].
Klinische Pädiatrie 2005;217(1):36-40.
2005: Muhammad Faiyaz-Ul-Haque; Syed Zaidi; L M King; Sayedul Haque; M Patel; Mahmud Ahmad; Teepu Siddique; Wasim Ahmad; Lap-Chee Tsui; Daniel H Cohn
Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes.
Clinical genetics 2005;67(1):93-7.
2004: Muhammad Faiyaz-Ul-Haque; Wasim Ahmad; Syed Zaidi; S Hussain; Sayedul Haque; Mahmud Ahmad; Daniel H Cohn; Lap-Chee Tsui
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis).
Clinical genetics 2004;66(2):144-51.
2004: Muhammad Faiyaz-Ul-Haque; Syed Zaidi; Mariam Al-Ali; Mariam S Al-Mureikhi; Shelley Kennedy; Ghalia Al-Thani; Lap-Chee Tsui; Ahmad S Teebi
A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type.
American journal of medical genetics. Part A 2004;128A(1):39-45.
2004: Muhammad Arshad Rafiq; Muhammad Ansar; Saqib Mahmood; Sayedul Haque; Muhammad Faiyaz-Ul-Haque; Suzanne M Leal; Wasim Ahmad
A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis.
The Journal of investigative dermatology 2004;123(1):247-8.
2004: Bryan Lo; Muhammad Faiyaz-Ul-Haque; Brenda L Banwell; Susan Blaser; A D Paterson; Lap-Chee Tsui; Ahmad S Teebi
The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23.
Clinical genetics 2004;65(2):137-42.
2003: Bryan Lo; Muhammad Faiyaz-Ul-Haque; Shelley Kennedy; Richard I Aviv; Lap-Chee Tsui; Ahmad S Teebi
Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubism.
American journal of medical genetics. Part A 2003;121A(1):37-40.
2003: Muhammad Arshad Rafique; Muhammad Ansar; Syed Muhammad Jamal; Sajid Malik; Muhammad Sohail; Muhammad Faiyaz-Ul-Haque; Sayedul Haque; Suzanne M Leal; Wasim Ahmad
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.
European journal of human genetics : EJHG 2003;11(8):623-8.
2003: Muhammad Ansar; Mohammad Amin ud Din; Muhammad Arshad; Muhammad Sohail; Muhammad Faiyaz-Ul-Haque; Sayedul Haque; Wasim Ahmad; Suzanne M Leal
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.
European journal of human genetics : EJHG 2003;11(1):77-80.
2002: Muhammad Faiyaz-Ul-Haque; Wasim Ahmad; Abdul Wahab; Sayedul Haque; anser azim; Syed Zaidi; Ahmad S Teebi; Mahmud Ahmad; Daniel H Cohn; Teepu Siddique; Lap-Chee Tsui
Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia.
American journal of medical genetics 2002;111(1):31-7.
2002: Muhammad Faiyaz-Ul-Haque; Wasim Ahmad; Syed Zaidi; Sayedul Haque; Ahmad S Teebi; Mahmud Ahmad; Daniel H Cohn; Lap-Chee Tsui
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome).
Clinical genetics 2002;61(6):454-8.
1998: Markus M Nöthen; Sven Cichon; Ina R Vogt; S Hemmer; Roland Kruse; Michael Knapp; Tobias Höller; Muhammad Faiyaz-Ul-Haque; Sayedul Haque; Peter Propping; M Ahmad; Marcella Rietschel
A gene for universal congenital alopecia maps to chromosome 8p21-22.
American journal of human genetics 1998;62(2):386-90.
1998: Wasim Ahmad; Muhammad Faiyaz-Ul-Haque; V Brancolini; HC Tsou; S ul Haque; HaMut Lam; Vincent M Aita; J Owen; M deBlaquiere; J Frank; Peter B Cserhalmi-Friedman; A Leask; John A McGrath; M Peacocke; M Ahmad; Jurg Ott; Angela M Christiano
Alopecia universalis associated with a mutation in the human hairless gene.
Science (New York, N.Y.) 1998;279(5351):720-4.