M. Alkan - Concepedia

Author

M. Alkan

Rutgers New Jersey Medical School

Also Known As

Alkan, M, M Alkan, M. Alkan, Mualla Alkan, Muallâ Alkan

Publications

440

Citations

H-Index

Concepts

All Affiliations

Rutgers New Jersey Medical School Universitätskinderklinik Rutgers, The State University of New Jersey Medizinische Hochschule Hannover University Children’s Hospital Basel

About

M. Alkan is an author at Rutgers New Jersey Medical School specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	390
2	Molecular Genetics	4	4	175
3	Public Health	3	3	118
4	Biology	1	1	46
5	Cell Biology	1	1	172

M. Alkan

Publications

415

Citations

H-Index

Page 1

	Year	Citations
Association between gene expression profile and tumor invasion in oral squamous cell carcinoma Gökçe Törüner, Celal Ülger, M. Alkan, Cancer Genetics and Cytogenetics Tumor InvasionGene Expression ProfileOncogenic AgentMedicinePathology	2004	172
DETECTION OF POLYMORPHISMS AT CYTOSINE PHOSPHOGUANADINE DINUCLEOTIDES AND DIAGNOSIS OF HAEMOPHILIA B CARRIERS Peter R. Winship, D. Jasper G. Rees, M. Alkan The Lancet Genetic AnalysisHaplotype DeterminationGenetic TestingMolecular Diagnostic TechniquesMedicine	1989	75
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome. Rossella Tupler, L Bortotto, E. Bühler, Journal of Medical Genetics CytogeneticsGeneticsPolymorphic ProbesMolecular GeneticsParental Origin	1992	46
Linkage relationships and allelic associations of the cystic fibrosis locus and four marker loci J. Schmidtke, Michael Krawczak, M. Schwartz, Human Genetics Allelic VariantMarker LociGenetic DisorderMedicineGenetics	1987	35
Another model for the inheritance of Rett syndrome Erica M. Bühler, Naseem Malik, M. Alkan American Journal of Medical Genetics InfertilityDevelopmental BiologyMendelian DisorderGenetic DisorderRett Syndrome	1990	32
Expression profiling reveals MSX1 and EphB2 expression correlates with the invasion capacity of Wilms tumors Albert Chetcuti, Safiye Aktaş, Nicole Mackie, Pediatric Blood & Cancer	2011	25
Arrangement of DYZ1 and DYZ2 repeats on the human Y-chromosome: a case with presence of DYZ1 and absence of DYZ2 E. Manz, M. Alkan, E. Bühler, Molecular and Cellular Probes ChromatinChromosome DynamicsDevelopmental BiologyCytogeneticsGenetic Disorder	1992	19
Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation. M. Alkan, Gian Paolo Ramelli, Hans Hirsiger, PubMed CytogeneticsGeneticsPathologySitu HybridisationPresumptive Monosomy 21	2002	11

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