Britt Marie Anderlid

Author

Karolinska Institutet

Also Known As

Britt Marie Anderlid

Publications

534

Citations

H-Index

Concepts

All Affiliations

Karolinska Institutet Karolinska University Hospital Istituti di Ricovero e Cura a Carattere Scientifico Azienda Ospedaliera Universitaria Senese Heidelberg University

About

Britt Marie Anderlid is an author at Karolinska Institutet specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	280
2	Education	1	1	42
3	Social Sciences	1	1	97
4	Child Development	1	1	42
5	Molecular Genetics	1	1	15

Britt Marie Anderlid

Publications

416

Citations

H-Index

Page 1

	Year	Citations
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologyHeterozygous VariantsKmt2e CauseGenetics	2019	97
Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome Vittoria Disciglio, Caterina Lo Rizzo, Maria Antonietta Mencarelli, American Journal of Medical Genetics Part A	2014	96
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, European Journal of Human Genetics Genetic DisorderCandidate RegionsGeneticsGynecologyDeletion 9P	2009	84
First-degree relatives of young children with autism spectrum disorders: Some gender aspects Mats Eriksson, Joakim Westerlund, Britt Marie Anderlid, Research in Developmental Disabilities Child PsychologyFirst-degree RelativesPsychiatryAutism Spectrum DisordersPediatrics	2012	42
Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients Jacqueline Schoumans, Josephine Wincent, Michela Barbaro, European Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsGenetic Epidemiology	2006	42
3p25.3 microdeletion of GABA transporters <i>SLC6A1</i> and <i>SLC6A11</i> results in intellectual disability, epilepsy and stereotypic behavior Nicola Dikow, Bianca Maas, Stephanie Karch, American Journal of Medical Genetics Part A	2014	40
De novo deletion of chromosome 11q13.4–q14.3 in a boy with microcephaly, ptosis and developmental delay Josephine Wincent, Jacqueline Schoumans, Britt Marie Anderlid European Journal of Medical Genetics Developmental BiologyCytogeneticsGenetic DisorderGeneticsPathology	2009	15

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