Anna Erlandson

430 total citations
13 papers, 327 citations indexed

About

Anna Erlandson is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Anna Erlandson has authored 13 papers receiving a total of 327 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cognitive Neuroscience. Recurrent topics in Anna Erlandson's work include Genetics and Neurodevelopmental Disorders (5 papers), Glycosylation and Glycoproteins Research (4 papers) and Epigenetics and DNA Methylation (4 papers). Anna Erlandson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Glycosylation and Glycoproteins Research (4 papers) and Epigenetics and DNA Methylation (4 papers). Anna Erlandson collaborates with scholars based in Sweden, United States and Belgium. Anna Erlandson's co-authors include Bengt Hagberg, Tommy Martinsson, Cecilia Bjursell, Jan Wahlström, Mårten Kyllerman, B. Kristiansson, Helena Stibler, Lena Samuelsson, Mihailo Vujic and Hudson H. Freeze and has published in prestigious journals such as Journal of Investigative Dermatology, Human Mutation and Human Genetics.

In The Last Decade

Anna Erlandson

13 papers receiving 321 citations

Peers

Countries citing papers authored by Anna Erlandson

Since Specialization

Citations

This map shows the geographic impact of Anna Erlandson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Anna Erlandson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Erlandson more than expected).

Fields of papers citing papers by Anna Erlandson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Erlandson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Anna Erlandson. The network helps show where Anna Erlandson may publish in the future.

Co-authorship network of co-authors of Anna Erlandson

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Erlandson. A scholar is included among the top collaborators of Anna Erlandson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anna Erlandson. Anna Erlandson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Deletion of the MGMT gene in familial melanoma 2014 ·Genes Chromosomes and Cancer ·(unknown), Maria Yhr, Anna Erlandson, Tommy Martinsson, Charlotta Enerbäck	3
2	Aetiology of severe mental retardation and further genetic analysis by high‐resolution microarray in a population‐based series of 6‐ to 17‐year‐old children 2011 ·Acta Paediatrica ·(unknown), (unknown), Anna Erlandson, Mårten Kyllerman	10
3	Early Infantile Onset ‘‘Congenital’’ Rett Syndrome Variants: Swedish Experience Through Four Decades and Mutation Analysis 2011 ·Journal of Child Neurology ·(unknown), Anna Erlandson, Mårten Kyllerman, (unknown), (unknown), (unknown), Bengt Hagberg	12
4	Epigenetic mutations in CDKN2A in western Swedish families with hereditary malignant melanoma 2008 ·Molecular Medicine Reports ·Charlotta Enerbäck, (unknown), Anna Erlandson	8
5	Novel CDKN2A Mutations Detected in Western Swedish Families with Hereditary Malignant Melanoma 2007 ·Journal of Investigative Dermatology ·Anna Erlandson, (unknown), Ann‐Marie Wennberg, (unknown), Charlotta Enerbäck	8
6	MECP2 Abnormality Phenotypes: Clinicopathologic Area With Broad Variability 2005 ·Journal of Child Neurology ·Anna Erlandson, Bengt Hagberg	31
7	Multiplex Ligation-Dependent Probe Amplification (MLPA) Detects Large Deletions in the MECP2 Gene of Swedish Rett Syndrome Patients 2003 ·Genetic Testing ·Anna Erlandson, Lena Samuelsson, Bengt Hagberg, Mårten Kyllerman, Mihailo Vujic, Jan Wahlström	55
8	Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations 2001 ·Human Genetics ·Anna Erlandson, Cecilia Bjursell, Helena Stibler, B. Kristiansson, Jan Wahlström, Tommy Martinsson	28
9	MECP2 mutation screening in Swedish classical Rett syndrome females 2001 ·European Child & Adolescent Psychiatry ·Anna Erlandson, Birgitta Hallberg, Bengt Hagberg, J. Wahlström, Tommy Martinsson	15
10	Denaturing High-Performance Liquid Chromatography Is a Suitable Method for PMM2 Mutation Screening in Carbohydrate-Deficient Glycoprotein Syndrome Type IA Patients 2000 ·Genetic Testing ·Anna Erlandson, Helena Stibler, B. Kristiansson, Jan Wahlström, Tommy Martinsson	7
11	Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia) 2000 ·Human Mutation ·Gert Matthijs, Els Schollen, Cecilia Bjursell, Anna Erlandson, Hudson H. Freeze, Faiqa Imtiaz, Søren K. Kjærgaard, Tommy Martinsson, M. Schwartz, Nathalie Séta, Sandrine Vuillaumier‐Barrot, Vibeke Westphal, Bryan Winchester	122
12	PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families 2000 ·Human Mutation ·Cecilia Bjursell, Anna Erlandson, Margareta Nordling, Staffan Nilsson, (unknown), Helena Stibler, B. Kristiansson, Tommy Martinsson	27
13	PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families 2000 ·Human Mutation ·Cecilia Bjursell, Anna Erlandson, Margareta Nordling, Staffan Nilsson, Jan Wahlström, Helena Stibler, B. Kristiansson, Tommy Martinsson	1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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