Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Marc Lalande | Researchclopedia

Back to researchers

Marc Lalande

University of Connecticut

109

Works

9,692

Citations

46

h-index

79

i10-index

Research Topics

Genetic Syndromes and Imprinting Epigenetics and DNA Methylation Prenatal Screening and Diagnostics

Affiliations

Boston Children's Hospital1983–1999

Howard Hughes Medical Institute1989–1999

Université Toulouse III - Paul Sabatier2000–2000

Harvard University1984–1999

University of Connecticut2001–2023

Top Works

UBE3A/E6-AP mutations cause Angelman syndrome

Tatsuya Kishino,Marc Lalande,et al.

19971,321 citations

Genomic variations and chromosomal abnormalities

DNA Repair Mechanisms

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls,Joan H.M. Knoll,et al.

1989884 citations

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

Jérôme Cavaillé,Karin Buiting,et al.

2000592 citations

The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain

Claire Rougeulle,Heather Glatt,et al.

1997420 citations

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes

Stormy J. Chamberlain,Pin-Fang Chen,et al.

2010319 citations

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

Claire Rougeulle,Carlos Cardoso,et al.

1998308 citations

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region

Tayfun Özçelık,Stuart E. Leff,et al.

1992295 citations

Analysis of the Set of GABAA Receptor Genes in the Human Genome

Joseph Simon,Hironobu Wakimoto,et al.

2004254 citations

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Philippe Jay,Claire Rougeulle,et al.

1997245 citations