Published Research

Research Title	Authors	Journal	Volume & Page Numbers	Year
The M694I/M694I genotype: a genetic risk factor of AA-amyloidosis in a group of Algerian patients with familial Mediterranean fever.	Ait-Idir D, Djerdjouri B, Bouldjennet F, Taha RZ, El-Shanti H, Sari-Hamidou R, Khellaf G, Benmansour M, Benabadji M, Haddoum F	Eur J Med Genet	60(3):149-153	2017
Biallelic SCN10A Mutations in Neuromuscular Disease and Epileptic Encephalopathy	Kambouris M, Thevenon J, Soldatos A, Cox A, Stephen J, Ben-Omran T, Al-Sarraj Y, Boulos H, Bone W, Mullikin JC, NISC Comparative Sequencing Program, Masurel-Paulet A, St Onge J, Dufford Y, Chantegret C, Thauvin-Robinet C, Al-Alami J, Faivre L, Riviere JB, Gahl WA, Bassuk AG, Malicdan MCV, El-Shanti H	Ann Clin Trans Neurol	4(1):112-1131	2017
Type II diabetes mellitus and hyperhomocysteinemia: a complex interaction	Platt DE, Hariri E, Salameh P, Merhi M, Sabbah N, Helou M, Mouzaya F, Nemer R, Al-Sarraj Y, El-Shanti H, Abchee AB, Zalloua PA	Diabetology & Metabolic Syndrome	9(1):19	2017
Citation classics in chronic granulomatous disease: A bibliometric analysis	Bakri F, Adwan M, El-Shanti H	Int J Clin Exp Med	10(4):6204-6220	2017
A Chromosomal Microdeletion of 15q in A Female Patient with Epilepsy, ID and Autism Spectrum Disorder: A Case Report	Ahram DF, Al-Sarraj Y, Taha RZ, Elhag S, Al-Shaban F, El-Shanti H, Kambouris M	Clin Case Rep	5(6): 1013-1017	2017
Mosaic Partial Pericentromeric Trisomy 8 and Maternal Uniparental Disomy in a Male Patient with Autism Spectrum Disorder.	Ahram DF, Stambouli D, Syrogianni A, Al-Sarraj Y, Gerou S, El-Shanti H, Kambouris M	Clin Case Rep	4(12):1125-1131	2016
Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase	Paemka L, Mahajan VB, Ehaideb SN, Skeie JM, Tan MC, Wu S, Cox AJ, Sowers LP, Gecz J, Jolly L, Ferguson PJ, Darbro B, Schneider A, Scheffer IE, Carvill GL, Mefford HC, El-Shanti H, Wood S, Manak JR, Bassuk AG	PLoS Genet	11(3): e1005022	2015
Overlap of Familial Mediterranean Fever and Hyper-IgD Syndrome in an Arabic Kindred.	Moussa T, Aladbe B, Taha R, Remmers EF, El-Shanti H, Fathalla B	Journal of Child Immunology	35(3):249-253	2015
Interleukin-1 Receptor Antagonist Deficiency with a novel mutation; late onset and a successful treatment with canakinumab: a case report	Ulusoy E, Karaca NE, El-Shanti H, Kilicoglu E, Aksu G, Kutukculer N	Journal of Medical Case Reports	23(1):145	2015
Caffeine impact on metabolic syndrome components is modulated by a CYP1A2 variant	Platt DE, Ghassibe-Sabbagh M, Salloum AK, Mouzaya F, Gauguier D, Al-Sarraj Y, El-Shanti H, Zalloua PA, Abchee AB	Ann Nutr Metab	21;68(1):1-11	2015
Genetic testing and genomic analysis: a debate on ethical, social and legal issues in the Arab world with a focus on Qatar	El Shanti H, Chouchane L, Badii R, Gallouzi I, Gasparini P	J Transl Med	13(1):358	2015
A Novel De Novo PSTPIP1 Mutation in a Boy with Pyogenic Arthritis, Pyoderma Gangrenosum, Acne (PAPA) Syndrome	Fathalla B, Al-Wahadneh AM, Al-Mutawa M, Kambouris M, El-Shanti H	Clin Exp Rheumatol	32(6):956-958	2014
A Novel Missense Mutation in SRD5A3 Causes Congenital Disorder of Glycosylation Type I [Cerebello-Ocular Syndrome]	Al-Sarraj Y, Ben-Omran T, Tolefat M, Bejaoui Y, El-Shanti H, Kambouris M	Journal of Inborn Errors of Metabolism and Screening	2: 2326409814550528	2014
Utilization of Gene Mapping and Candidate Gene Mutation Screening for Diagnosing Clinically Equivocal Conditions: A Norrie Disease Case Study	Chini V, Stambouli D, Nedelea FM, Filipescu GA, Mina D, Kambouris M, El-Shanti H	Eye Science	29(2):104-107	2014
Mutations in Zinc Finger 407 [ZNF407] Cause an Autosomal Recessive Cognitive Impairment Syndrome	Kambouris M, Ben-Omran T, Maroun RC, Al-Sarraj Y, Errafii K, Ali R, Boulos H, Curmi PA, El-Shanti H	Orphanet Journal of Rare Diseases	9:80	2014
Multivariate epidemiologic analysis of type 2 diabetes mellitus risks in the Lebanese population	Ghassibe-Sabbagh M, Deeb M, Salloum AK, Mouzaya F, Haber M, Al-Sarraj Y, Chami Y, Akle Y, Hirbli K, Nemr R, Ahdab R, Platt DE, Abchee AB, El-Shanti H, Zalloua PA	Diabetology & Metabolic Syndrome	6(1):89	2014
Distal Trisomy 10q Syndrome, Report of a Patient with Duplicated q24.31 – qter, Autism Spectrum Disorder and Unusual Features	Al-Sarraj Y, Abul Al-Khair H, Taha RZ, Khattab N, El-sayed ZH, Elhusein B, El-Shanti H	Clinical Case Reports	2(5):201-205	2014
T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility	Ghassibe-Sabbagh M, Haber M, Salloum AK, Al-Sarraj Y, Akle Y, Hirbli K, Romanos J, Mouzaya F, Gauguier D, Platt DE, El-Shanti H, Zalloua PA	Scientific Reports	4:7351	2014
Chronic recurrent multifocal osteomyelitis and deficiency of interleukin-1-receptor antagonist	Sakran W, Shalev SA, El-Shanti H, Uziel Y	Pediatr Infect Dis J	32(1):94	2013
Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction	Sowers LP, Loo L, Wu Y, Campbell E, Ulrich JD, Wu S, Paemka L, Wassink T, Meyer K, Bing X, El-Shanti H, Usachev YM, Ueno N, Manak RJ, Shepherd AJ, Ferguson PJ, Darbro BW, Richerson GB, Mohapatra DP, Wemmie JA, Bassuk AG. Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction. Mol Psychiatry. 2013; 18(10):1077-1089	Mol Psychiatry	18(10):1077-1089	2013
PRICKLE1 interaction with SYNAPSIN1 reveals a role in Autism Spectrum Disorders	Paemka L, Mahajan VB, Skeie JM, Sowers LP, Ehaideb SN, Gonzalez-Alegre P, Sasaoka T, Tao H, Miyagi A, Ueno N, Takao K, Miyakawa T, Wu S, Darbro BW, Ferguson PJ, Pieper AA, Britt JK, Wemmie JA, Rudd DS, Wassink T, El-Shanti H, Mefford HC, Carvill GL, Manak RJ, Bassuk AG	PLoS1	8(12): e80737	2013
Spectrum Of Mutations and Carrier Frequency of Familial Mediterranean Fever Gene in the Algerian Population	Ait-Idir D, Khilan A, Djerdjouri B, El-Shanti H	Rheumatology	50:2306-2310	2011
Mutations in Prickle Orthologs Cause Seizures in Flies, Mice, and Humans	65) Tao H, Manak JR, Sowers L, Mei X, Kiyonari H, Abe T, Dahdaleh NS, Yang T, Wu S, Chen S, Fox MH, Gurnett C, Montine T, Bird T, Shaffer LG, Rosenfeld JA, McConnell J, Madan-Khetarpal S, Berry-Kravis E, Griesbach H, Saneto RP, Scott MP, Antic D, Reed J, Boland R, Ehaideb SN, El-Shanti H, Mahajan VB, Ferguson PJ, Axelrod JD, Lehesjoki AE, Fritzsch B, Slusarski DC, Wemmie J, Ueno N, Bassuk AG	Am J Hum Genet	88:138-149	2011
A Novel Mutation of IL1RN in the Deficiency of Interleukin-1-Receptor Antagonist Syndrome: Description of Two Unrelated Cases from Brazil	Jesus AA, Osman M, Silva CA, Kim PW, Pham T-H, Gadina M, Yang B, Bertola DR, Carneiro-Sampaio M, Ferguson PJ, Renshaw BR, Schooley K, Brown M, Al-Dosari A, Alami J, Sims JE, Goldbach-Mansky R, El-Shanti H	Arth Rheum	63:4007-4017	2011
A homozygous mutation in ADAMTSL4 causes autosomal recessive isolated ectopia lentis	Ahram D, Sato TS, Kohailan A, Tayeh MK, Chen S, Leal S, Al-Salem M, El-Shanti H	Am J Hum Genet	84:274-278	2009
An Autoinflammatory Disease with Deficiency of the Interleukin-1 Receptor Antagonist	Aksentijevich I, Masters SL, Ferguson PJ, Dancey P, Frenkel J, van Royen-Kerkhoff A, Laxer R, Tedgård U, Cowen E, Pham T-H, Booty M, Estes JD, Sandler NG, Plass N, Stone DL, Turner ML, Hill S, Butman JA, Schneider R, Babyn P, El-Shanti HI, Pope E, Barron K, Bing X, Laurence A, Lee C-CR, Chapelle D, Clarke GI, Ohson K, Nicholson M, Gadina M, Yang B, Korman BD, Gregersen PK, van Hagen PM, Hak AE, Huizing M, Rahman P, Douek DC, Remmers EF, Kastner DL, Goldbach-Mansky R.	N Engl J Med	360:2426-2437	2009
Independent Introduction of Two Lactase Persistence Alleles into Human Populations Reflect Different History of Adaptation to Milk Culture	Enattah NS, Jensen TGK, Nielsen M, Lewinski R, Kuokkanen M, Rasinpera H, El-Shanti H, Seo JK, Alifrangis M, Khalil I, Natah A, Ali A, Natah S, Comas D, Mehdi SQ, Groop L, Vestergaard EM, Imtiaz F, Rashed MS, Meyer B, Troelsen J, Peltonen L	Am J Hum Genet	82:57-72	2008
The Infevers auto-inflammatory mutation online registry. The 2007 update: New genes and new functions	Milhavet F, Cuisset L, Hofmann H, Slim R, El-Shanti H, Aksentijevich I, Lesage S, Waterham H, Wise C, de Menthiere CS, Touitou I	Hum Mutat	29:803-808	2008
Breakpoint Localization using array-CGH in Three Siblings with an Unbalanced 4q;16q Translocation and Childhood Apraxia of Speech (CAS)	Shriberg LD, Jakielskie, El-Shanti H	Am J Med Genet A	146A:2227-2233	2008
Neutrophil dysfunction in a family with a SAPHO-like phenotype	Ferguson PJ, Lokuta MA, Muhle L, El-Shanti H, Bing X, Huttenlocher A	Arth Rheum	58:3264-3269	2008
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonic epilepsy-ataxia syndrome	Bassuk AG, Wallace RH, Buhr A, Buller A, Shimojo M, Miyata S, Chen S, Gonzalez-Alegre P, Griesbach HL, Shu W, Nashelsky M, Vladar EK, Antic D, Ferguson PJ, Cirak S, Voit T, Scott MP, Axelrod JD, Gurnett C, Daoud AS, Afawi Z, Neufeld MY, Korczyn AD, Kivity S, Mazarib A, Straussberg R, Walid S, Slusarski DC, Berkovic SF, El-Shanti HI	Am J Hum Genet	83:572-581	2008
A splice site mutation confirms the role of LPIN2 in Majeed Syndrome	Al-Musawi ZS, Al-Saad KK, Ijadi-Magsoodi R, El-Shanti H, Ferguson PJ	Arth Rheum	56:960-964	2007
A Homozygous Mutation in a Novel Zinc Finger Protein, ERIS, is responsible for Wolfram Syndrome 2	Amr S, Heisey C, Zhang M, Xia X-J, Shows KH, Ajlouni K, Pandya A, Satin LS, El-Shanti H, Shiang R	Am J Hum Genet	81:673-683	2007
Chronic Recurrent Multifocal Osteomyelitis (CRMO): An illustrative case	Ochoa L, Ferguson PJ, El-Shanti HI	J Musculoskel Med	24:340-347	2007
Chronic Recurrent Multifocal Osteomyelitis: A Concise Review and Genetic Update	El-Shanti H, Ferguson PJ	Clin Orthop Rel Res	462:11-19	2007
Autoinflammatory bone disorders	Ferguson PJ, El-Shanti H	Curr Opin Rheum	19:492-498	2007
A missense mutation in pstpip2 is associated with murine autoinflammatory disorder chronic multifocal Osteomyelitis	Ferguson PJ, Bing X, Vasef MA, Ochoa LA, Mahgoub A, Waldschmidt TJ, Tygrett LT, Schlueter AJ, El-Shanti H	Bone	38:41-47	2006
Novel sequence variants in the TMIE gene in families with autosomal recessive non-syndromic hearing impairment	Santos RLP, El-Shanti H, Sikandar S, Lee K, Bhatti A, Yan K, Chahrour M, McArthur N, Pham T, Mahasneh AA, Ahmad W, Leal SM	J Mol Med	84:226-231	2006
A distinct autosomal recessive ataxia maps to chromosome 12 in an inbred family from Jordan	El-Shanti H, Daoud A, Sadoon A, Leal S, Chen S, Lee K, Spiegel R	Brain Dev	28:353-357	2006
Familial Mediterranean Fever in Arabs	El-Shanti H, Majeed HA, El-Khateeb M	Lancet	367:1016-1024	2006
Consanguinity and its implications on practice, research and policy	Teebi AS, El-Shanti HI	Lancet	367:970-971	2006
Familial Mediterranean Fever: A prevalent condition amongst the Arabs	El-Shanti H, Majeed HA, El-Khateeb M	Jordan Medical Journal	40:46-64	2006
Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 Jordan	Al-Alami J, Tanner SM, Tayeh MK, de la Chapelle A, El-Shanti H	Saudi Med J	26:1061-1064	2005
The spectrum of Familial Mediterranean Fever gene mutations in Arabs: Report of a large series	Majeed HA, El-Khateeb M, El-Shanti H, Abu Rabaiha Z, Tayeh M, Najib D	Semin Arthritis Rheum	34:813-818	2005
Homozygous Mutations in LPIN2 are Responsible for the Syndrome of Chronic Recurrent Multifocal Osteomyelitis and Congenital Dyserythropoietic Anemia (Majeed Syndrome)	Ferguson PJ, Chen S, Tayeh M, Ochoa LA, Leal S, Pelet A, Munnich A, Lyonnet S, Majeed HA, El-Shanti H	J Med Genet	42:551-557	2005
Effects of short term Metformin administration on androgens in Diabetic Men	Shegem NS, Alsheek Nasir AM, Batieha AM, El-Shanti H, Ajlouni KM	Saudi Med J	25:75-78	2004
Radiologic findings in Wolfram syndrome	Haddidy A, Jarrah N, Al-Till M, El-Shanti H, Ajlouni K	Saudi Med J	25:638-641	2004
Further delineation of El-Shanti syndrome	El-Shanti H	Eur J pediatr	163:761-762	2004
Familial Mediterranean fever mutation frequencies and carrier rates among a mixed Arabic population	Al-Alami JR, Tayeh MD, Najib DA, Abu-Rubaiha ZA, Majeed HA, Al-Khateeb MS, El-Shanti HI	Saudi Med J	24:1055-1059	2003
Hypogonadotrophic hypogonadism, short stature, cerebellar ataxia, rod-cone retinal dystrophy, and hypersegmented neutrophils: A novel disorder or a new variant of Boucher-Neuhauser syndrome	Jbour A, Mubaidin A, Till M, El-Shanti H, Hadidi A, Ajlouni KM	J Med Genet	40:e2	2003
Alopecia universalis congenita, XY gonadal dysgenesis, and laryngomalacia: A novel autosomal recessive disorder	El-Shanti H, Ahmad M, Ajlouni K	Eur J pediatr	162:36-40	2003
Risk factors for childhood epilepsy: A case-control study from Irbid, Jordan	Daoud AS, Batieha A, Bashtawi M, El-Shanti H	Seizure	12:171-174	2003
Familial Mediterranean Fever and Renal Disease	El-Shanti H	Saudi J Kidney Dis Transplant	14:378-385	2003
Linkage analysis of a large inbred family with autosomal recessive vitamin B12 deficiency	Al-Alami J, Tayeh M, Al-Sheyyab M, El-Shanti H	Saudi Med J	23:1251-1256	2002
Diversity in polyp pathology and distribution of Familial Juvenile Polyposis Syndrome	Al-Jaberi TM, El-Shanti H	Saudi Med J	23:328-331	2002
The pattern of peripheral blood chromosomal abnormalities in Northern Jordan	El-Shanti H, Al-Alami J	Saudi Med J	23:1552-1554	2002
Cerebellar hypoplasia, Hypergonadotrophic hypogonadism, Retinitis pigmentosa, Alopecia, Microcephaly, Psychomotor retardation, and short stature: “D- CHRAMPS Syndrome”	Hiyasat D, Dehyyat MA, Ajlouni S, Mubaidin A, Till M, Hadidi A, El-Shanti H, Ajlouni KM	Eur J Ped	161:170-172	2002
Wolfram syndrome: Identification of a phenotypic and genotypic variant from Jordan	Ajlouni K, Jarrah N, Al-Khateeb M, El-Zaheri M, El-Shanti H, Lidral A	Am J Med Genet	115:61-65	2002
Genotype / phenotype correlations in Arab patients with Familial Mediterranean Fever	Majeed HA, El-Shanti H, Al-Khateeb MS, Abu Rabihah ZA	Semin Arthritis Rheum	31:371-37	2002
Bleeding tendency in Wolfram Syndrome: A newly identified feature with phenotype / genotype correlation	Al-Sheyyab M, Jarrah N, Younis E, Shennak MM, Haddidi A, Awidi A, El-Shanti H, Ajlouni K	Eur J Ped	160:243-246	2001
Homozygosity mapping places the acrodermatitis enteropathica gene on chromosome 8q24.3	Wang K, Pugh EW, Griffin S, Doheny KF, Mostafa WZ, Al-aboosi MM, El-Shanti H, Gitschier J	Am J Hum Genet	68:1055-1060	2001
Raine syndrome: Report of a case with hand and foot anomalies	Mahafza T, El-Shanti H, Omari H	Clin Dysmorph	10:227-229	2001
The impact of genetic diseases on Jordanians: Strategies towards prevention.	El-Shanti H	Journal of biomedicine & biotechnology	1:46-48	2001
Familial Mediterranean Fever	El-Shanti H	Saudi Med J	22:104-109	2001
Craniofacial anthropometric measurements in a population of normal Jordanian newborns	El-Shanti H, Al-Lahham MB, Batieha A	J Med Liban	48:23-28	2000
Chediak-Higashi syndrome: A report of eight cases from three families	Al-Sheyyab M, Daoud AS, El-Shanti H	Indian Pediatr	37:69-75	2000
Homozygosity mapping identifies an additional locus for Wolfram syndrome on 4q	El-Shanti H, Lidral A, Jarrah N, Druhan L, Ajlouni K	Am J Hum Genet	66:1229-1236	2000
The effect of trifluoperazine on the genotoxicity of Bleomycin in cultured human lymphocytes	Sadiq MF, Khabour OF, El-Shanti HE, Samawi HM	Drug Chem Toxicol	23:361-369	2000
Induction of chromosomal aberrations by the rhodium(III) complex cis-[Rh(biq)(2)Cl(2)]Cl in cultured human lymphocytes	Sadiq MF, Zaghal MH, El-Shanti H	Mutagenesis	15:375-378	2000
On mice and men: An autosomal recessive syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anemia	Majeed HA, El-Shanti H, Al-Rimawi H, Al- Masri N	J Pediatr	137:441-442	2000
Familial disorder of sex determination in seven individuals from three related sibships	Jarrah N, El-Shanti H, Kheir A, Obeidat FN, Haddidi A, Ajlouni K	Eur J Ped	159:912-8	2000
Fine mapping of progressive pseudorheumatoid dysplasia: A tool for heterozygote identification	Alkhateeb A, Al-Alami J, Leal SM, El-Shanti H	Genetic Testing	3:329-333	1999
Wolfram syndrome in triplets with newly recognized features	Jarrah NS, El-Shanti H, Shennak MM, Ajlouni KM	Ann Saudi Med	19:132-134	1999
The effect of desferroxamine in acute hemolytic anemia of G-6-PD deficiency	Al-Rimawi H, Al-Sheyyab M, Batieha A, El-Shanti H, Abukteish F	Acta Hematologica	101:145-148	1999
Familial Mediterranean Fever in children: the expanded clinical profile	Majeed HA, Rawashdeh M, El-Shanti H, Qubain H, Khuri-Bulos N, Shahin HM	Q J Med	92:309-318	1999
Henoch-Schonlein purpura and streptococcal infection: a prospective case-control study	Al-Sheyyab M, Batieha A, El-Shanti H, Daoud A	Ann Trop Paediatr	19:253-5	1999
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia	Hurvitz JR, Suwairi WM, Van Hul W, El-Shanti H, Superti-Furga A, Roudier J, Holderbaum D, Pauli RM, Herd JK, Hul EV, Rezai-Delui H, Legius E, Le Merrer M, Al-Alami J, Bahabri SA, Warman ML	Nat Genet	23:94-98	1999
A clinical study of a large inbred kindred with pure familial spastic paraplegia	El-Shanti H, Daoud AS, Batieha A	Brain Dev	21:478-482	1999
A nonsense mutation in the retinal-specific guanylate cyclase gene is the cause of Leber congenital amaurosis in a large inbred-kindred from Jordan	El-Shanti H, Al-Salem M, El-Najjar M, Ajlouni K, Beck J, Sheffield VC, Stone EM	J Med Genet	36:862-865	1999
The assignment of the gene responsible for progressive pseudorheumatoid dysplasia to chromosome six and examination of COL10A1 as a candidate gene	El-Shanti H, Murray JC, Semina EV, Buetow KH, Scherpbier T, Al-Alami J	Eur J Hum Genet	6:251-256	1998
Normative standards of trunk and limb anthropometric measurements for Jordanian newborns	El-Shanti H, Al-Lahham MB, Batieha A	Saudi Med J	19:702-706	1998
Fanconi anemia and hypothyroidism	Al-Sheyyab M, El-Shanti H, Daoud AS, Gharabieh N, Ektiesh F	Ann Saudi Med	18:58-59	1998
An outbreak of Poliomyelitis in Jordan: Clinical observations	Daoud AS, Al-Sheyyab M, Al-Qudah A, Khouri-Bulos N, El-Shanti H	Indian Pediatr	34:51-54	1997
A rare case of a liveborn with free, de novo and partial trisomy 12 and an unusual phenotype	El-Shanti H, Khasawneh M, Hulsburg D, Major H, Patil S	Ann Genet	40:175-180	1997
Progressive pseudorheumatoid dysplasia: Report of a family and review.	El-Shanti H, Omari HZ, Qubain HI	J Med Genet	34:559-563	1997
Neural tube defects in Northern Jordan	Daoud AS, Al-Kaysi F, El-Shanti H, Batieha A, Obeidat A, Al-Sheyyab M	Saudi Med J	17:78-81	1996
Henoch-Schonlein Purpura: Clinical experience and contemplation on a streptococcal association	Al-Sheyyab M, El-Shanti H, Ajlouni S, Batieha A, Daoud AS	J Trop Pediatr	42:200-203	1996
Neonatal meningitis in northern Jordan	Daoud AS, Al-Sheyyab M, Abu Ekteish F, Obeidat A, Ali AA, El-Shanti H. Neonatal meningitis in northern Jordan. J Trop pediatr 1996; 42:267-270	J Trop pediatr	42:267-270	1996
Autosomal recessive lamellar ichthyosis and acute lymphoblastic leukemia	Al-Sheyyab M, El-Shanti H, Todd D, Shurman A	Eur J Hum Genet	4:105-107	1996
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: Further delineation of the critical region	Mears AJ, El-Shanti H, Murray JC, McDermid HE, Patil SR	Am J Hum Genet	57:667-673	1995
The clinical spectrum of Henoch-Schonlein purpura in infants and young children	Al-Sheyyab M, El-Shanti H, Ajlouni S, Sawalha D, Daoud AS	Eur J Pediatr	154:969-972	1995
Transient improvement of congenital lactic acidosis in a male with pyruvate decarboxylase deficiency treated with dichloroacetate	Toth PP, El-Shanti H, Eivins S, Rhead WJ, Klein JM	J Pediatr	123:427-431	1993
Epidermal nevus syndrome: Subgroup with neuronal migration defects	El-Shanti H, Bell WE., Waziri MH	J Child Neurol	7:29-34	1992

Published Research // <![CDATA[ _spBodyOnLoadFunctionNames.push("setupPageDescriptionCallout"); // ]]>

Published Research