Anna Lindstrand

5.4k citations
84 papers · 1.5k indexed · h-index 22

Impact in

  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
    • Congenital heart defects research

Papers in

    • Genomic variations and chromosomal abnormalities 39
    • Genomics and Rare Diseases 22
    • Genetics and Neurodevelopmental Disorders 11
    • Genetic Syndromes and Imprinting 6
    • Congenital heart defects research 13
    • Genomics and Chromatin Dynamics 8
    • RNA modifications and cancer 7

Anna Lindstrand

81 papers receiving 1.4k citations

Peers

Anna Lindstrand
Comparison fields: 5 of 99
  • Genetics 827
  • Molecular Biology 882
  • Cell Biology 134
  • Cancer Research 118
  • Pediatrics, Perinatology and Child Health 135
Replace Katherine Lachlan with:
Katherine Lachlan United Kingdom
Francisco Martı́nez Spain
David Geneviève France
Christel Thauvin‐Robinet France
Victoria Mok Siu Canada
Marianne Till France
Tommaso Pippucci Italy
Julie Désir Belgium
Ewa Obersztyn Poland
Eva Holmberg Sweden
Anna Lindstrand relative to Katherine Lachlan United Kingdom Katherine Lachlan's profile →
Citations per field
00.5×1.5×2.1×
Katherine Lachlan · 1×
Citations per year

Countries citing papers authored by Anna Lindstrand

Since Specialization
Citations

This map shows the geographic impact of Anna Lindstrand'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 Lindstrand with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Lindstrand more than expected).

Fields of papers citing papers by Anna Lindstrand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Lindstrand. 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 Lindstrand. The network helps show where Anna Lindstrand may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Anna Lindstrand, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna Lindstrand Line = papers co-authored together Anna Lindstrand links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20255
2 20251
3 20241
4 20235
5 202317
6 20231
7 20237
8 20231
9 20222
10 20225
11 202210
12 202011
13 202011
14 201915
15 20199
16 201918
17 201930
18 201811
19 201819
20 200952

About Anna Lindstrand

Anna Lindstrand is a scholar working on Genetics, Molecular Biology, Urology, Cancer Research and Plant Science, having authored 84 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (39 papers), Genomics and Rare Diseases (22 papers), Chromosomal and Genetic Variations (16 papers), Congenital heart defects research (13 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Chromatin Dynamics (8 papers), RNA modifications and cancer (7 papers) and Genetic Syndromes and Imprinting (6 papers). The work is most often cited by research in Genetics (827 citations), Molecular Biology (882 citations), Cell Biology (134 citations), Cancer Research (118 citations) and Pediatrics, Perinatology and Child Health (135 citations). Anna Lindstrand has collaborated with scholars based in Sweden, United States and Finland. Frequent co-authors include Ann Nordgren, Wolfgang Hofmeister, Daniel Nilsson, Maria Pettersson, Raquel Vaz, Outi Mäkitie, Jesper Eisfeldt, Claudia M.B. Carvalho, Elisabeth Blennow and Britt‐Marie Anderlid. Their work appears in journals such as Human Mutation, Frontiers in Genetics, Clinical Genetics, PLoS ONE and Scientific Reports.

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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