Nandita Quaderi - Concepedia

Concepedia

Author

Nandita Quaderi

Telethon Institute Of Genetics And Medicine ORCID

Also Known As

N Quaderi, N. A. Quaderi, N. Quaderi, N.A. Quaderi, NANDITA QUADERI, Nandita A Quaderi, Nandita A. Quaderi, Nandita Quaderi

24

Publications

1.1K

Citations

12

H-Index

24

Concepts

All Affiliations

Telethon Institute Of Genetics And Medicine St Mary's Hospital Institute of Genetics and Biophysics King's College London Children's Hospital of Philadelphia

NQ

About

Nandita Quaderi is an author at Telethon Institute Of Genetics And Medicine specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	938
2	Molecular Genetics	6	6	712
3	Cell Biology	4	4	274
4	Molecular Biology	2	2	179
5	Natural Sciences	1	1	138

Nandita Quaderi

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12

Publications

1.1K

Citations

12

H-Index

	Year	Citations
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22 Nandita Quaderi, Susann Schweiger, Karin Gaudenz, Nature Genetics Developmental AnomalyOpitz G/bbb SyndromeDevelopmental BiologyMendelian DisorderGenetic Disorder	1997	367
Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development Alessandro Bulfone, Salvador Martı́nez, Valeria Marigo, Mechanisms of Development Developmental BiologyEpendymaBrain DevelopmentDevelopmental GeneticsGenetics	1999	154
Isolation, physical mapping, and Northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 Maurizio D’Esposito, Nandita Quaderi, Alfredo Ciccodicola, Mammalian Genome ChromatinMethyl Cpg-binding ProteinX-linked Human GeneGeneticsNatural Sciences	1996	138
Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain Karin Gaudenz, Erich Roessler, Nandita Quaderi, The American Journal of Human Genetics Developmental AnomalyOpitz G/bbb SyndromeDevelopmental BiologyMendelian DisorderGenetic Disorder	1998	69
MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During Development Georg Buchner, Eugenio Montini, Grazia Andolfi, Human Molecular Genetics	1999	60
Genetic and Physical Mapping of a Gene Encoding a Methyl CpG Binding Protein, Mecp2, to the Mouse X Chromosome Nandita Quaderi, Richard R. Meehan, P Tate, Genomics Knockout MouseChromatinMouse X ChromosomeDevelopmental BiologyGenetics	1994	58
The Opitz syndrome gene MID1 is essential for establishing asymmetric gene expression in Hensen’s node Alessandra Granata, Nandita Quaderi Developmental Biology Transcriptional RegulationDevelopmental BiologyGenetic DisorderDevelopmental GeneticsGenetics	2003	48
The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse David A. Adler, Nandita Quaderi, S. D. M. Brown, Mammalian Genome ChromatinGenome InstabilityChromatin RemodelingEpigenetic ChangeGenetics	1995	41
Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome Alessandra Granata, Dawn Savery, Jamïlé Hazan, Developmental Biology Mid ProteinsDevelopmental BiologyCell DivisionGenetic DisorderMedicine	2004	32
Identification of a New EGF-Repeat-Containing Gene from Human Xp22: A Candidate for Developmental Disorders Georg Buchner, Ugo Orfanelli, Nandita Quaderi, Genomics Developmental BiologyGenetic DisorderGeneticsDevelopmental DisordersNew Egf-repeat-containing Gene	2000	31

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