Britt Marie Anderlid

Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome

Vittoria Disciglio, Caterina Lo Rizzo, Maria Antonietta Mencarelli et al. · American Journal of Medical Genetics Part A · 2014 · 99 citations

Life Sciences, Genetics, Molecular Genetics +17

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

Anne O’Donnell‐Luria, Lynn Pais, Víctor Faùndes et al. · The American Journal of Human Genetics · 2019 · 99 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA

Michela Barbaro, Antonio Balsamo, Britt Marie Anderlid et al. · European Journal of Human Genetics · 2009 · 84 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

First-degree relatives of young children with autism spectrum disorders: Some gender aspects

Mats Eriksson, Joakim Westerlund, Britt Marie Anderlid et al. · Research in Developmental Disabilities · 2012 · 43 citations

Medicine, Genetics, Pediatrics +7

Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients

Jacqueline Schoumans, Josephine Wincent, Michela Barbaro et al. · European Journal of Human Genetics · 2006 · 43 citations

Life Sciences, Genetics, Molecular Genetics +8