Özden Sanal - Concepedia

Author

Özden Sanal

Also Known As

Justin S. Goodman, O SANAL, O Sanal, O. Sanal, Ozden Sanal, Özden Sanal, Sanal, O, Steven M. Holland, Ö Sanal, Ö. Sanal

232

Publications

17.9K

Citations

H-Index

142

Concepts

All Affiliations

Hacettepe University Hospital Hacettepe University Hôpital Necker-Enfants Malades Inserm Université Paris Cité

ÖS

About

Özden Sanal is an author at Hacettepe University Hospital specializing in medicine, autoimmune disease, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	72	9.6K
2	Allergy	13	15	966
3	Health Sciences	7	7	291
4	Public Health	1	1	36
5	Biochemistry	1	1	20

Özden Sanal

122

Publications

16.3K

Citations

H-Index

Page 1

	Year	Citations
A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase Kinneret Savitsky, Anat Bar‐Shira, Shlomit Gilad, Science	1995	2.8K
Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2) Patrick Revy, Taro Muto, Yves Lévy, Cell Mendelian DisorderAutoimmune DiseaseGenetic DisorderGeneticsImmunology	2000	1.6K
Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency Despina Moshous, Isabelle Callebaut, Régina de Chasseval, Cell Primary ImmunodeficiencyIs MutatedGenome InstabilityImmunogeneticsAutoimmune Disease	2001	893
Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly Dietke Buck, Laurent Malivert, Régina de Chasseval, Cell Primary ImmunodeficiencyIs MutatedMedicineImmunodeficienciesImmunology	2006	697
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23 Richard A. Gatti, İzzet Berkel, Elena Boder, Nature Ataxia-telangiectasia GeneGenetic DisorderGeneticsMolecular GeneticsDisease Gene Identification	1988	685
Clinical spectrum of X-linked hyper-IgM syndrome Jacov Levy, Teresa Espanol-Boren, Carolin Thomas, The Journal of Pediatrics Mendelian DisorderAutoimmune DiseaseGenetic DisorderFragile X SpectrumPathology	1997	655
Mycobacterial Disease and Impaired IFN-γ Immunity in Humans with Inherited ISG15 Deficiency Dusan Bogunovic, Minji Byun, Larissa A. Durfee, Science	2012	541
Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation Xianqin Zhang, Dusan Bogunovic, Béatrice Payelle‐Brogard, Nature InflammationCytokineImmunologyChronic InflammationInnate Immunity	2014	539
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene Élodie Pastural, Franck J. Barrat, Rémi Dufourcq-Lagelouse, Nature Genetics Myosin-va GeneGenetic DisorderGeneticsPathogenesisGriscelli Disease Maps	1997	456
Mutations in <i>STAT3</i> and <i>IL12RB1</i> impair the development of human IL-17–producing T cells Ludovic de Beaucoudrey, Anne Puel, Orchidée Filipe‐Santos, The Journal of Experimental Medicine	2008	428

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