Nadezda Kosyakova - Concepedia

Author

Nadezda Kosyakova

Jena University Hospital

Also Known As

J.E. Womack, Kosyakova, Nadezda, N Kosyakova, N. Kosyakova, N. V. Kosyakova, N.V. Kosyakova, Nadezda Kosyakova

135

Publications

2.8K

Citations

H-Index

Concepts

All Affiliations

Jena University Hospital Friedrich Schiller University Jena Universidade Federal de São Carlos Max Planck Institute for the Science of Human History Universidade Federal de São Paulo

About

Nadezda Kosyakova is an author at Jena University Hospital specializing in genetics, medicine, and chromosome biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	34	1.1K
2	Biology	13	13	392
3	Natural Sciences	10	10	293
4	Public Health	7	7	197
5	Engineering	2	2	65

Nadezda Kosyakova

Publications

Citations

H-Index

Page 1

	Year	Citations
Molecular Definition of High-resolution Multicolor Banding Probes: First Within the Human DNA Sequence Anchored FISH Banding Probe Set Anja Weise, Kristin Mrasek, Ina Fickelscher, Journal of Histochemistry & Cytochemistry MicroscopyCytogeneticsGeneticsDna AnalysisMolecular Biology	2008	104
First Molecular Cytogenetic High Resolution Characterization of the NIH 3T3 Cell Line by Murine Multicolor Banding Christine Leibiger, Nadezda Kosyakova, Hasmik Mkrtchyan, Journal of Histochemistry & Cytochemistry ChromatinGenome InstabilityNih 3T3Cell DivisionCytogenetics	2013	99
Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8,18, and 21 in three patients Joanna Pietrzak, Kristin Mrasek, Ewa Obersztyn, Journal of Applied Genetics ChromatinCytogeneticsGenetic DisorderGeneticsMolecular Cytogenetic Characterization	2007	96
Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations Mariana Moysés‐Oliveira, Roberta dos Santos Guilherme, Anelisa Gollo Dantas, Fertility and Sterility Primary AmenorrheaChromosome DynamicsCell DivisionGenetic DisorderGenetics	2015	65
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences Thomas Liehr, Markus Stümm, R.‐D. Wegner, Cytogenetic and Genome Research	2009	55
The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2 Lusine Nazaryan, Eunice G. Stefanou, Claus Hansen, European Journal of Human Genetics Complex RearrangementsCytogeneticsGeneticsMolecular GeneticsGenomics	2013	54
Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes Thomas Liehr, Martina Merkaš, Lukrecija Brečević, Current Genomics	2010	53
Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy Yasemin Soysal, Sevim Balcı, Kuyaş Hekimler, American Journal of Medical Genetics Part A CytogeneticsGeneticsMolecular GeneticsMild Mental RetardationEpigenetics	2009	51
Array painting using microdissected chromosomes to map chromosomal breakpoints Liesbeth Backx, Hilde Van Esch, Cindy Melotte, Cytogenetic and Genome Research ChromatinGenome InstabilityChromosomal BreakpointsEngineeringGenetics	2007	49
Early Embryonic Chromosome Instability Results in Stable Mosaic Pattern in Human Tissues Hasmik Mkrtchyan, Madeleine Gross, Sophie Hinreiner, PLoS ONE Cnv Mosaic RatiosCytogeneticsLymphocyte DevelopmentGeneticsGenomics	2010	48

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