Çiğdem Altay - Concepedia

Author

Çiğdem Altay

Also Known As

C Altay, C. ALTAY, C. Altay, CIGDEM ALTAY, Cigdem A. Altay, Cigdem Altay, Cumhur Altay, C¸. ALTAY, Çigdem Altay, Çiğdem Altay

155

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Hacettepe University Augusta University Hacettepe University Hospital University of Amsterdam

ÇA

About

Çiğdem Altay is an author at Hacettepe University specializing in medicine, hematology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	31	1.1K
2	Health Sciences	10	11	390
3	Public Health	7	7	311
4	Natural Sciences	2	2	34
5	Arts	1	1	16

Çiğdem Altay

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group. Laurence Bonhomme‐Faivre, Philippe Guardiola, Cathryn M. Lewis, PubMed	2000	216
Application of Endonuclease Mapping to the Analysis and Prenatal Diagnosis of Thalassemias Caused by Globin-Gene Deletion Stuart H. Orkin, Blanche P. Alter, Çiğdem Altay, New England Journal of Medicine	1978	208
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance. Jerome R. Lo Ten Foe, M. L. Kwee, Martin A. Rooimans, PubMed	1997	203
The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H disease Stuart H. Orkin, John Old, Herbert Lazarus, Cell ImmunohematologyHb H DiseaseGenetic DisorderGeneticsInherited Metabolic Disease	1979	182
Importance of RDW value in differential diagnosis of hypochrome anemias Deniz Aslan, Fatma Gümrük, Aytemiz Gürgey, American Journal of Hematology	2001	114
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene Stephan M. Tanner, Zhongyuan Li, James D. Perko, Proceedings of the National Academy of Sciences	2005	106
Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene Mario Wijker, Sarah Herterich, CGM van Berkel, European Journal of Human Genetics BiologyGenetic AnalysisHeterogeneous SpectrumAllelic VariantGenetic Disorder	1999	104
Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia Günay Balta, Nazmiye Yüksek, Emel Özyürek, American Journal of Hematology	2003	102
Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes C. Öner, Çiğdem Altay, Aytemiz Gürgey, Blood	1992	98
PAI‐1 gene 4G/5G genotype: A risk factor for thrombosis in vessels of internal organs Günay Balta, Çiğdem Altay, Aytemiz Gürgey American Journal of Hematology	2002	95

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