Sotabase

Career

· Researcher, University of Amsterdam, Complex Cyber Infrastructure (CCI) group2024–

Publications (65)

Female adnexal tumor of probable wolffian origin. A Distinctive Pathologic Entity
Cancer · 1973
167
cited
Elucidating the spectrum of α-thalassemia mutations in Iran
2007
56
cited
Neu-Laxova syndrome: report of a case and comments.
American journal of medical genetics · 1987
32
cited
Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis
American Journal of Medical Genetics. Part A · 2009
27
cited
Elucidating the spectrum of alpha-thalassemia mutations in Iran.
Haematologica · 2007
26
cited
Human testosterone-oestradiol binding globulin in health and disease.
Acta Endocrinologica · 1977
25
cited
Lung hypoplasia and its associated major congenital abnormalities in perinatal death: An autopsy study of 850 cases
Indian Journal of Pediatrics · 2009
13
cited
Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18
European Journal of Human Genetics · 2011
12
cited
Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations
Iranian journal of child neurology · 2013
10
cited
A case of megalencephalic leukoencephalopathy with subcortical cysts in an Iranian consanguineous family.
2009
7
cited
Widespread aplasia cutis congenita in sibs with PLEC1 and ITGB4 variants
American Journal of Medical Genetics. Part A · 2019
7
cited
Science of breeding and heredity from ancient Persia to modern Iran
Indian Journal of Human Genetics · 2012
3
cited
Ambiguous Genitalia and Review of the Cases
2007
2
cited
An/micr-Ophthalmia, Cleft Lip/Palate, and Short Limbs: A New Syndrome Simulating a Short Rib Syndrome
Fetal and Pediatric Pathology · 2012
2
cited
A review on prenatal screening and diagnosis
2009
2
cited
A case of complete tetraploidy in amniotic fluid culture with normal karyotype in the repeat
2006
1
cited
Acquired Mutation and Reversion of the Neutrophil Elastase Gene, ELA2 , in Kostmann Syndrome and Cyclic Neutropenia Suggest that Some Mutations Cause Neutropenia while Others Paradoxically Suppress It.
2004
1
cited
Berardinelli-Seip congenital lipodystrophy: Report of a case and review of literature
2009
1
cited
Comparison of Early and Mid-Trimester Amniocentesis in 1459 Amniotic Fluid Cultures
2006
1
cited
Freeman-Sheldon syndrome: report of 6 cases
2006
1
cited
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