Wanda M. Gerding - Concepedia

Author

Wanda M. Gerding

Also Known As

Gerding, Wanda M., Gerding, Wanda Maria, W. M. Gerding, W.M. Gerding, Wanda M Gerding, Wanda M. Gerding, Wanda M. Gerding (288711), Wanda Maria Gerding

Publications

Citations

H-Index

Concepts

All Affiliations

Ruhr University Bochum Witten/Herdecke University Technische Universität Dresden University Hospitals of the Ruhr-University of Bochum TU Dortmund University

About

Wanda M. Gerding is an author at Ruhr University Bochum specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	511
2	Social Sciences	5	5	183
3	Health Sciences	3	3	107
4	Public Health	2	2	78
5	Biology	1	1	23

Wanda M. Gerding

Publications

880

Citations

H-Index

Page 1

	Year	Citations
Handedness and the X chromosome: The role of androgen receptor CAG-repeat length Larissa Arning, Sebastian Ocklenburg, Stefanie Schulz, Scientific Reports	2015	111
PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness Larissa Arning, Sebastian Ocklenburg, Stefanie Schulz, PLoS ONE Cerebral AsymmetryAllelic VariantHandedness Category ComparisonGeneticsHuman Polymorphism	2013	94
Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization Sebastian Ocklenburg, Larissa Arning, Constanze Hahn, Behavioural Brain Research Subunit Gene Grin2bSynaptic PlasticityMolecular NeuroscienceNeuroanatomyGenetics	2011	56
Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in <scp>AML</scp>/<scp>MDS</scp> patients Wanda M. Gerding, Marco Tembrink, Verena Nilius‐Eliliwi, International Journal of Cancer CytogeneticsMixed-phenotype Acute LeukemiaGeneticsGenetic EpidemiologyPathology	2022	55
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene Gabriele Dekomien, Conni Vollrath, Elisabeth Petrasch‐Parwez, Neurogenetics Ocular DiseaseRetinaProgressive Retinal AtrophyOphthalmologyExperimental Ophthalmology	2009	50
FOXP2 variation modulates functional hemispheric asymmetries for speech perception Sebastian Ocklenburg, Larissa Arning, Wanda M. Gerding, Brain and Language Cognitive ScienceHealth SciencesNeurolinguisticsNeuroscienceSpeech Motor Control	2013	49
Ccdc66 null mutation causes retinal degeneration and dysfunction Wanda M. Gerding, Sabrina Schreiber, Tobias Schulte-Middelmann, Human Molecular Genetics Protein Ccdc66Developmental BiologyRetinaOphthalmologyExperimental Ophthalmology	2011	47
Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization Sebastian Ocklenburg, Larissa Arning, Wanda M. Gerding, PLoS ONE GeneticsNeurolinguisticsGenetic EpidemiologyLanguage LateralizationSocial Sciences	2013	46
Exome Sequencing Reveals<i>AGBL5</i>as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families Simone Kastner, Ina-Janine Thiemann, Gabriele Dekomien, Investigative Ophthalmology & Visual Science	2015	41
Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF Wanda M. Gerding, Judith Koetting, Jörg T. Epplen, Neuromuscular Disorders Novel MutationHereditary MotorSensory NeuropathyMendelian DisorderGenetic Disorder	2009	40

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