Şükrü Palanduz - Concepedia

Author

Şükrü Palanduz

Also Known As

Easwar,, S PALANDUZ, S Palanduz, S Palandüz, S. PALANDUZ, S. Palanduz, S??kr?? Palanduz, SUKRU PALANDUZ, Sukru Palanduz, Sükrü Palanduz

143

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Istanbul University Humboldt-Universität zu Berlin Trakya University Charité - Universitätsmedizin Berlin

ŞP

About

Şükrü Palanduz is an author at Istanbul University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	20	748
2	Health Sciences	3	3	92
3	Biochemistry	3	3	98
4	Public Health	2	2	33
5	Biology	1	1	129

Şükrü Palanduz

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes Seval Türkmen, Gabriele Gillessen‐Kaesbach, Peter Meinecke, European Journal of Human Genetics BiologySotos SyndromeDevelopmental BiologyOther Overgrowth PhenotypesFrequent Finding	2003	129
Brucellosis in a mother and her young infant: Probable transmission by breast milk Ayşe Palandüz, Şükrü Palanduz, Kerim Güler, International Journal of Infectious Diseases Maternal ImmunizationAnimal DischargesZoonotic DiseasePathogenesisPediatrics	2000	102
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis Christine P. Diggle, David Parry, Clare V. Logan, Human Mutation	2012	95
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction Elena Bonora, Francesca Bianco, Lina Cordeddu, Gastroenterology Chronic Intestinal Pseudo-obstructionGastroenterologyPathologyClinical GastroenterologyGastrointestinal Pathology	2015	80
Plasma antioxidants and type 2 diabetes mellitus. Şükrü Palanduz, Evin Ademoğlu, Cahide Gökkuşu, PubMed Metabolic SyndromePlasma Superoxide DismutaseControl GroupDiabetes ManagementBiochemistry	2001	69
Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1 Georg C. Schwabe, Seval Türkmen, Gundula Leschik, American Journal of Medical Genetics Part A	2003	66
OXIDANT AND ANTIOXIDANT SYSTEMS IN NIDDM PATIENTS: INFLUENCE OF VITAMIN E SUPPLEMENTATION Cahide Gökkus ̨u, Şükrü Palanduz, Evin Ademoğlu, Endocrine Research	2001	64
REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis Yavuz Bayram, Janson J. White, Nursel Elçioğlu, The American Journal of Human Genetics FibrosisMendelian DisorderGeneticsPathologyMedicine	2017	58
A Study of Serological Markers of Hepatitis B and C Viruses in Istanbul, Turkey S. Erden, Suna Büyüköztürk, Semra Çalangu, Medical Principles and Practice	2003	48
In VitroChromosomal Radiosensitivity in Common Variable Immune Deficiency Şükrü Palanduz, Ayşe Palandüz, Ayper Somer, Clinical Immunology and Immunopathology Autoimmune DiseaseImmunodeficienciesRadiation EffectImmunologyAutoimmunity	1998	40

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