Concepedia

Maninder Kaur

MK

Statistics

Publications

39

Citations

4K

H-Index

27

Active since

1992

Affiliations

Children's Hospital of Philadelphia(Current)

University of Pennsylvania

Drexel University

Greater Baltimore Medical Center

The University of Tokyo

Maninder Kaur is an author at Children's Hospital of Philadelphia specializing in genetics, molecular genetics, and life sciences.

ORCID

Publications per year

1992–2023

39

Publications

39

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

Ian D. Krantz, Jennifer McCallum, Cheryl DeScipio et al. · Nature Genetics · 2004 · 722 citations · Full text

, , +6

HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle

Matthew A. Deardorff, Masashige Bando, Ryuichiro Nakato et al. · Nature · 2012 · 576 citations · Full text

, , +8

Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation

Matthew A. Deardorff, Maninder Kaur, Dinah Yaeger et al. · The American Journal of Human Genetics · 2007 · 522 citations · Full text

, , +6

NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations

Lynette A. Gillis, Jennifer McCallum, Maninder Kaur et al. · The American Journal of Human Genetics · 2004 · 317 citations · Full text

, , +14

Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells

Jinglan Liu, Zhe Zhang, Masashige Bando et al. · PLoS Biology · 2009 · 231 citations · Full text

, , +17

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