Nicole Maas - Concepedia

Author

Nicole Maas

KU Leuven

Also Known As

N M C Maas, N. MC Maas, Nicole M C Maas, Nicole M.C. Maas, Nicole Maas

Publications

698

Citations

H-Index

Concepts

All Affiliations

KU Leuven Hôpital Necker-Enfants Malades Assistance Publique – Hôpitaux de Paris

About

Nicole Maas is an author at KU Leuven specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	365
2	Molecular Genetics	2	2	179
3	Natural Sciences	1	1	23
4	Public Health	1	1	156
5	Molecular Biology	1	1	23

Nicole Maas

Publications

644

Citations

H-Index

Page 1

	Year	Citations
Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH) Nicole Maas, Griet Van Buggenhout, Femke Hannes, Journal of Medical Genetics	2007	178
Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis Joris Vermeesch, Cindy Melotte, Guy Froyen, Journal of Histochemistry & Cytochemistry Array CghGenetic TestingCytogeneticsGeneticsComparative Genomic Hybridization	2005	156
The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients Griet Van Buggenhout, Conny M.A. van Ravenswaaij‐Arts, Nicole Maas, European Journal of Medical Genetics Clinical DisordersMolecular CharacterizationGene Deletion DataGenetic DisorderGenetics	2005	137
The <i>C20orf133</i> gene is disrupted in a patient with Kabuki syndrome Nicole Maas, Tom Van de Putte, Cindy Melotte, Journal of Medical Genetics	2007	70
Lack of effect of polymorphisms in dopamine metabolism related genes on imaging of TRODAT‐1 in striatum of asymptomatic volunteers and patients with Parkinson's disease David R. Lynch, P. David Mozley, Set Sokol, Movement Disorders Neuroimaging BiomarkersDopamine TransporterGeneticsMedicineNeuropharmacology	2003	49
A dysmorphic boy with 4qter deletion and 4q32.3‐34.3 duplication: Clinical, cytogenetic, and molecular findings Griet Van Buggenhout, Nicole Maas, Jean‐Pierre Fryns, American Journal of Medical Genetics Part A	2004	31
The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random. Nicole Maas, Steven Van Vooren, Femke Hannes, PubMed Other 4P16GeneticsMolecular BiologyMolecular GeneticsEpigenetics	2007	23

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