Citation Impact
Citing Papers
Chromosome Abnormalities and Genetic Counseling
2011
The Istanbul consensus workshop on embryo assessment: proceedings of an expert meeting
2011 Standout
Who's afraid of the big bad Wolff?: “Wolff's law” and bone functional adaptation
2006 Standout
The changing scene of amyotrophic lateral sclerosis
2013
Effects of genetic correction on the differentiation of hair cell-like cells from iPSCs with MYO15A mutation
2016
Calcium's Role in Mechanotransduction during Muscle Development
2014 Standout
The β-Thalassemias
1999 Standout
The role of autophagy in neurodegenerative disease
2013 Standout
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
2020 Standout
Morphological and cytogenetic analysis of human giant oocytes and giant embryos
2002
WNT and β-catenin signalling: diseases and therapies
2004 Standout
1 The population genetics of the haemoglobinopathies
1998
Abnormal constitutional karyotypes in patients with neuroblastoma: a report of four new cases and review of 47 others in the literature
2003
Cytogenetic analysis of giant oocytes and zygotes to assess their relevance for the development of digynic triploidy
2002
Limb bone bilateral asymmetry: variability and commonality among modern humans
2005 Standout
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
Digynic triploid infant surviving for 46 days
1999
WNT signaling in bone homeostasis and disease: from human mutations to treatments
2013 Standout
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Wnt/β-Catenin Signaling and Disease
2012 Standout
Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases
2009 Standout
The DNA Damage Response: Making It Safe to Play with Knives
2010 Standout
Gestational trophoblastic disease I: epidemiology, pathology, clinical presentation and diagnosis of gestational trophoblastic disease, and management of hydatidiform mole
2010 Standout
8 The population genetics of the haemoglobinopathies
1993
Developmental perspectives on copy number abnormalities of the 22q11.2 region
2010
Rapid Trisomy Diagnosis (21, 18, and 13) Using Fluorescent PCR and Short Tandem Repeats: Applications for Prenatal Diagnosis and Preimplantation Genetic Diagnosis
1998
Sickle-cell disease
2010 Standout
Neuroblastoma
2007 Standout
Conception to ongoing pregnancy: the 'black box' of early pregnancy loss
2002 Standout
World distribution of factor V Leiden
1995 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
Homozygous WNT3 Mutation Causes Tetra-Amelia in a Large Consanguineous Family
2004
Loss of ALS2/Alsin Exacerbates Motor Dysfunction in a SOD1H46R-Expressing Mouse ALS Model by Disturbing Endolysosomal Trafficking
2010
Pathology of Gestational Trophoblastic Disease
2003
Why are some genetic diseases common?
1993
Canalization, developmental stability, and morphological integration in primate limbs
2002
Liquid-Liquid Phase Separation in Biology
2014 Standout
THE WNT SIGNALING PATHWAY IN DEVELOPMENT AND DISEASE
2004 Standout
POLYPLOID INCIDENCE AND EVOLUTION
2000 Standout
Genetics of familial amyotrophic lateral sclerosis
2008
Calcium signaling via two-pore channels: local or global, that is the question
2009
Works of Seher Başaran being referenced
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally
1995
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation
2007
Molecular basis of ?-thalassemia in Turkey: detection of rare mutations by direct sequencing
1990
Isochromosome 18p Results from Maternal Meiosis II Nondisjunction
1996
A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family
2003
Tetra‐amelia, lung hypo‐/aplasia, cleft lip‐palate, and heart defect: A new syndrome?
1994
Partial Molar Appearance of the Placenta in Trisomy 13
2002
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis
2010
Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocation
2002
A hereditary bisatellite-dicentric supernumerary chromosome in a case of Cat-eye Syndrome
2008