Author

Mohammad Al-Haggar

Professor of Pediatrics, Chief of Genetics Unit, Mansoura University, Egypt - Cited by 581 - Molecular Biology

Biography

Dr Mohammad Al-Haggar is currently a Professor of Pediatrics and Genetics, Mansoura, Egypt. Received MBBCh in 1986, MSc in Pediatrics 1991, Diploma in Molecular Genetics, Tor Vergata Rome, Italy, PhD. 1994, MD.1995, Pediatrics & Genetics, Mansoura, Egypt. Awarded scholarship in Molecular Genetics 1993 for 6 months, Rome, Italy. 
Title
Cited by
Year
Endothelin-1 and leptin as markers of intrauterine growth restriction
MAS Nezar, AMA El-Baky, OAS Soliman, HAS Abdel-Hady, AM Hammad, ...The Indian Journal of Pediatrics 76, 485-488, 2009200
63
2009
Vitamin e and N-acetylcysteine as antioxidant adjuvant therapy in children with acute lymphoblastic leukemia
Y Al-Tonbary, M Al-Haggar, R El-Ashry, S El-Dakroory, H Azzam, A FoudaAdvances in Hematology 2009, 2009200
47
2009
Biofeedback and cognitive behavioral therapy for Egyptian adolescents suffering from chronic fatigue syndrome
MS Al-Haggar, ZA Al-Naggar, MA Abdel-SalamJournal of pediatric neurology 4 (03), 161-169, 2006200
39
2006
A novel homozygous p. Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome
M Al-Haggar, A Madej-Pilarczyk, L Kozlowski, JM Bujnicki, S Yahia, ...European journal of human genetics 20 (11), 1134-1140, 2012201
36
2012
Effect of maternal diabetes and hypercholesterolemia on fetal liver of albino Wistar rats
HIH El-Sayyad, MMS Al-Haggar, HA El-Ghawet, IHM BakrNutrition 30 (3), 326-336, 2014201
35
2014
Impact of long-term oral iron supplementation in breast-fed infants
N Abdelrazik, M Al-Haggar, H Al-Marsafawy, H Abdel-Hadi, R Al-Baz, ...The Indian Journal of Pediatrics 74, 739-745, 2007200
26
2007
Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia
A Settin, M Al Haggar, T Al Dosoky, R Al Baz, NM Abdelrazik, M Fouda, ...The Indian Journal of Pediatrics 74, 5-263, 2007200
25
2007
Cystinosis as a lysosomal storage disease with multiple mutant alleles: Phenotypic-genotypic correlations
M Al-HaggarWorld journal of nephrology 2 (4), 94, 2013201
19
2013
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family
M Al-Haggar, A Bakr, T Tajima, K Fujieda, A Hammad, O Soliman, ...Clinical and experimental nephrology 13, 288-294, 2009200
18
2009
Bioinformatics in high throughput sequencing: application in evolving genetic diseases
MM Al-Haggar, BA Khair-Allaha, MM Islam, ASA MohamedJ Data Mining Genomics Proteomics 4 (131), 2153-0602.1000131, 2013201
18
2013
Disruptive behavior in Down syndrome children: a cross-sectional comparative study
S Yahia, M El-Hadidy, AH El-Gilany, D Amdel-Hady, Y Wahba, ...Annals of Saudi medicine 34 (6), 517-521, 2014201
15
2014
Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia: Cases from Mansoura, Egypt
A Settin, M Al Haggar, T Al Dosok, R Al Baz, N Abdelrazik, M Fouda, ...Hematology 11 (5-6), 341-349, 2006200
14
2006
p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome
M Al-Haggar, S Yahia, K Damjanovich, N Ahmad, I Hamada, ...The Indian Journal of Pediatrics 78, 103-105, 2011201
14
2011
Single nucleotide polymorphism of IL4C-590T and IL4RA 175V and immunological parameters in Egyptian asthmatics with different clinical phenotypes
M Zedan, A Bakr, B Shouman, H Zaghloul, M Al-Haggar, M Zedan, ...J Allergy Ther 5 (189), 2, 2014201
13
2014
Fanconi Bickel syndrome: novel mutations in GLUT 2 gene causing a distinguished form of renal tubular acidosis in two unrelated Egyptian families
M Al-Haggar, O Sakamoto, A Shaltout, A El-Hawary, Y Wahba, ...Case Reports in Nephrology 2011, 2011201
12
2011
Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children’Hospital, Mansoura, Egypt
MS Al-Haggar, S Yahia, D Abdel-Hady, A Al-Saied, R Al-Kenawy, ...Indian Journal of Human Genetics 20 (1), 43, 2014201
11
2014
Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H‐syndrome
M Al‐Haggar, N Salem, Y Wahba, N Ahmad, L Jonard, D Abdel‐Hady, ...Pediatric Diabetes 16 (4), 305-316, 2015201
11
2015
Sporadic fibrodysplasia ossificans progressiva in an Egyptian infant with c. 617G> A mutation in ACVR1 gene: a case report and review of literature
M Al-Haggar, N Ahmad, S Yahia, A Shams, B Hasaneen, ...Case Reports in Genetics 2013, 2013201
10
2013
Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi–Bickel syndrome: revisited gene atlas for renumbering
M Al-Haggar, O Sakamoto, A Shaltout, A Al-Hawari, Y Wahba, ...Clinical and experimental nephrology 16, 604-6, 2012201
10
2012
Fanconi-Bickel syndrome as an example of marked allelic heterogeneity
M Al-HaggarWorld Journal of Nephrology 1 (3), 63, 2012201
8
2012

Referred From: https://scholar.google.com/citations?user=0cgEbiwAAAAJ&hl=en

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Citations 581
h-index 14
i10-index 24
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