Birgit Carlsson

1.8k total citations · 1 hit paper
25 papers, 1.3k citations indexed

About

Birgit Carlsson is a scholar working on Molecular Biology, Genetics and Biochemistry. According to data from OpenAlex, Birgit Carlsson has authored 25 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Biochemistry. Recurrent topics in Birgit Carlsson's work include Sulfur Compounds in Biology (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Glutathione Transferases and Polymorphisms (4 papers). Birgit Carlsson is often cited by papers focused on Sulfur Compounds in Biology (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Glutathione Transferases and Polymorphisms (4 papers). Birgit Carlsson collaborates with scholars based in Sweden, United States and United Kingdom. Birgit Carlsson's co-authors include Niklas Dahl, Peter Gustavsson, Joakim Klar, Hans Matsson, Dmitri Tentler, Björn Andersson, Gil Tchernia, Thiébaut-Noël Willig, Narla Mohandas and M Pettersson and has published in prestigious journals such as Nature Genetics, Analytical Biochemistry and Annals of Neurology.

In The Last Decade

Birgit Carlsson

25 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

1999 594 citations Peter Gustavsson, Björn Andersson et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Birgit Carlsson Sweden	16	838	303	133	107	87	25	1.3k
W. Putt United Kingdom	20	756 0.9×	375 1.2×	133 1.0×	90 0.8×	74 0.9×	44	1.3k
Christine Powers United States	20	768 0.9×	209 0.7×	331 2.5×	55 0.5×	77 0.9×	23	1.3k
L.-C. Tsui Canada	20	1.5k 1.8×	692 2.3×	147 1.1×	95 0.9×	108 1.2×	33	2.4k
Malka Nissim‐Rafinia Israel	21	1.8k 2.2×	258 0.9×	144 1.1×	103 1.0×	125 1.4×	37	2.5k
Sergio P. Acebrón Germany	16	1.3k 1.5×	230 0.8×	226 1.7×	125 1.2×	99 1.1×	22	1.6k
L.‐C. Tsui Canada	26	1.3k 1.6×	547 1.8×	131 1.0×	96 0.9×	100 1.1×	50	2.5k
Céline Schaeffer Italy	20	1.3k 1.5×	544 1.8×	131 1.0×	83 0.8×	62 0.7×	32	2.0k
Carol Saunders United States	22	744 0.9×	635 2.1×	95 0.7×	41 0.4×	108 1.2×	59	1.3k
Eileen Southon United States	19	1.0k 1.2×	320 1.1×	169 1.3×	187 1.7×	229 2.6×	32	1.7k
Irene E. Zohn United States	22	1.3k 1.6×	171 0.6×	257 1.9×	255 2.4×	123 1.4×	42	2.0k

Countries citing papers authored by Birgit Carlsson

Since Specialization

Citations

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

Fields of papers citing papers by Birgit Carlsson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgit Carlsson

This figure shows the co-authorship network connecting the top 25 collaborators of Birgit Carlsson. A scholar is included among the top collaborators of Birgit Carlsson 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 Birgit Carlsson. Birgit Carlsson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Entesarian, Miriam, Birgit Carlsson, Mahmoud Mansouri, et al.. (2009). A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population. American Journal of Medical Genetics Part A. 149A(3). 380–386. 11 indexed citations

Mansouri, Mahmoud, Jens Schuster, Jitendra Badhai, et al.. (2008). Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure. Human Molecular Genetics. 17(23). 3776–3783. 99 indexed citations

Mansouri, Mahmoud, Birgit Carlsson, Edward J. Davey, et al.. (2006). Molecular genetic analysis of a de novo balanced translocation t(6;17)(p21.31;q11.2) associated with hypospadias and anorectal malformation. Human Genetics. 119(1-2). 162–168. 14 indexed citations

Melin, Malin, Birgit Carlsson, Henrik Anckarsäter, et al.. (2006). Constitutional Downregulation of <i>SEMA5A</i> Expression in Autism. Neuropsychobiology. 54(1). 64–69. 63 indexed citations

Klar, Joakim, Bengt Åsling, Birgit Carlsson, et al.. (2005). RAR-related orphan receptor A isoform 1 (RORa1) is disrupted by a balanced translocation t(4;15)(q22.3;q21.3) associated with severe obesity. European Journal of Human Genetics. 13(8). 928–934. 15 indexed citations

Mansouri, Mahmoud, Lena Marklund, Peter Gustavsson, et al.. (2005). Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation. European Journal of Human Genetics. 13(8). 970–977. 94 indexed citations

Tentler, Dmitri, Maria Johansson, Maria Råstam, et al.. (2003). A candidate region for Asperger syndrome defined by two 17p breakpoints. European Journal of Human Genetics. 11(2). 189–195. 24 indexed citations

Tentler, Dmitri, Göran Brandberg, Catalina Betancur, et al.. (2001). A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint. American Journal of Medical Genetics. 105(8). 729–736. 16 indexed citations

NJÅLSSON, Runa, Katarina Steen Carlsson, B. Olin, et al.. (2000). Kinetic properties of missense mutations in patients with glutathione synthetase deficiency. Biochemical Journal. 349(1). 275–275. 24 indexed citations

10.

Matsson, Hans, Joakim Klar, Petter Gustavsson, et al.. (1999). Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia. Human Genetics. 105(5). 496–500. 43 indexed citations

11.

Gustavsson, Peter, Björn Andersson, M Pettersson, et al.. (1999). The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nature Genetics. 21(2). 169–175. 594 indexed citations breakdown →

12.

Cohen, Loren H., Eszter P. Vamos, Claudine Heinrichs, et al.. (1997). Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiency. European Journal of Pediatrics. 156(12). 935–938. 9 indexed citations

13.

Laporte, Jocelyn, Ling‐Jia Hu, Christine Kretz, et al.. (1997). Cloning and Characterization of an Alternatively Spliced Gene in Proximal Xq28 Deleted in Two Patients with Intersexual Genitalia and Myotubular Myopathy. Genomics. 41(3). 458–462. 32 indexed citations

14.

Manning, N. J., Norman Davies, S. E. Olpin, et al.. (1994). Prenatal diagnosis of glutathione synthase deficiency. Prenatal Diagnosis. 14(6). 475–478. 7 indexed citations

15.

Mayatepek, Ertan, Georg F. Hoffmann, Birgit Carlsson, Agne Larsson, & Katja Becker. (1994). Impaired Synthesis of Lipoxygenase Products in Glutathione Synthetase Deficiency. Pediatric Research. 35(3). 307–310. 32 indexed citations

16.

Mayatepek, Ertan, et al.. (1993). Deficient synthesis of cysteinyl leukotrienes in glutathione synthetase deficiency.. PubMed. 15(6). 245–52. 3 indexed citations

17.

Erasmus, Elardus, Lodewyk J. Mienie, Wilhelmine N. de Vries, et al.. (1992). Prenatal analysis in two suspected cases of glutathione synthetase deficiency. Journal of Inherited Metabolic Disease. 16(5). 837–843. 9 indexed citations

18.

Gustafsson, Jan, et al.. (1990). Cholesterol synthesis in patients with glutathione deficiency. European Journal of Clinical Investigation. 20(4). 470–474. 1 indexed citations

19.

Laurent, Torvard C., A. G. Ogston, Håkan Pertoft, & Birgit Carlsson. (1980). Physical chemical characterization of percoll. II. Size and interaction of colloidal particles. Journal of Colloid and Interface Science. 76(1). 133–141. 18 indexed citations

20.

Laurent, Torvard C., B. N. Preston, & Birgit Carlsson. (1974). Conformational Transitions of Polynucleotides in Polymer Media. European Journal of Biochemistry. 43(2). 231–235. 29 indexed citations

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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