Jan Wahlström

7.6k total citations
136 papers, 4.3k citations indexed

About

Jan Wahlström is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Jan Wahlström has authored 136 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Genetics, 34 papers in Molecular Biology and 29 papers in Physiology. Recurrent topics in Jan Wahlström's work include Genetics and Neurodevelopmental Disorders (29 papers), Genomic variations and chromosomal abnormalities (27 papers) and Sarcoidosis and Beryllium Toxicity Research (18 papers). Jan Wahlström is often cited by papers focused on Genetics and Neurodevelopmental Disorders (29 papers), Genomic variations and chromosomal abnormalities (27 papers) and Sarcoidosis and Beryllium Toxicity Research (18 papers). Jan Wahlström collaborates with scholars based in Sweden, United States and United Kingdom. Jan Wahlström's co-authors include Tommy Martinsson, Johan Grünewald, Christopher Gillberg, Anders Eklúnd, Dale T. Umetsu, Anders Oldfors, Fredrik Enlund, Oluf Andersen, Margareta Nordling and Rosemarie H. DeKruyff and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Jan Wahlström

130 papers receiving 4.1k citations

Peers

Countries citing papers authored by Jan Wahlström

Since Specialization

Citations

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

Fields of papers citing papers by Jan Wahlström

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jan Wahlström

This figure shows the co-authorship network connecting the top 25 collaborators of Jan Wahlström. A scholar is included among the top collaborators of Jan Wahlström 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 Jan Wahlström. Jan Wahlström 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

#	Work	Indexed citations
1	Enhanced CD8+ cytolytic T cell responses in the peripheral circulation of patients with sarcoidosis and non-Löfgren's disease 2017 ·Respiratory Medicine ·Venkata Ramanarao Parasa, Helena Forsslund, (unknown), D. Lorenz, Susanna Kullberg, Anders Eklúnd, Magnus Sköld, Jan Wahlström, Johan Grünewald, Susanna Brighenti	20
2	Gender differences in the T-cell profiles of the airways in COPD patients associated with clinical phenotypes 2016 ·International Journal of COPD ·Helena Forsslund, Mingxing Yang, (unknown), Reza Karimi, Sven Nyrén, Benita Engvall, Johan Grünewald, Heta Merikallio, Riitta Kaarteenaho, Jan Wahlström, Åsa M. Wheelock, C. Magnus Sköld	23
3	Publishing SNP Genotypes of Human Embryonic Stem Cell Lines: Policy Statement of the International Stem Cell Forum Ethics Working Party 2011 ·Stem Cell Reviews and Reports ·Bartha Maria Knoppers, Rosario Isasi, Nissim Benvenisty, (unknown), Geoffrey Lomax, Clive Morris, Thomas H. Murray, (unknown), (unknown), Genevra Richardson, Douglas Sipp, (unknown), Jan Wahlström, Guido de Wert, Fanyi Zeng	10
4	Fluorescence study of interphase nuclei and double Y chromosomes 2009 ·Hereditas ·Hans Olof Åkesson, Hans Forssman, Jan Wahlström	0
5	A case of trisomy-G with a simultaneous balanced D-D translocation 2009 ·Hereditas ·(unknown), Karl‐Göran Sabel, Jan Wahlström	0
6	Chromosome aberrations in patients with paranoid psychosis 2008 ·Hereditas ·Rolf Axelsson, Jan Wahlström	2
7	Allergen-Specific MHC Class II Tetramer+ Cells Are Detectable in Allergic, but Not in Nonallergic, Individuals 2006 ·The Journal of Immunology ·Claudia Macaubas, Jan Wahlström, (unknown), Thomas G. Forsthuber, Grete Sønderstrup, William W. Kwok, Rosemarie H. DeKruyff, Dale T. Umetsu	41
8	Genome‐wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non‐BRCA1/2 families: Suggestive linkage to 10q23.32‐q25.3 2006 ·Genes Chromosomes and Cancer ·Annika Bergman, Per Karlsson, (unknown), Tommy Martinsson, (unknown), Staffan Nilsson, Jan Wahlström, Arne Wallgren, Margareta Nordling	16
9	Analysis of Chromosome 5q31–32 and Psoriasis: Confirmation of a Susceptibility Locus but no Association with SNPs within SLC22A4 and SLC22A5 2006 ·Journal of Investigative Dermatology ·(unknown), (unknown), Staffan Nilsson, Annica Inerot, Jan Wahlström, Lena Samuelsson	19
10	Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2) 2005 ·European Journal of Human Genetics ·Homa Tajsharghi, Niklas Darín, (unknown), Mårten Kyllerman, Jan Wahlström, Tommy Martinsson, Anders Oldfors	30
11	Identification of Genomic Deletions of the APC Gene in Familial Adenomatous Polyposis by Two Independent Quantitative Techniques 2004 ·Genetic Testing ·Johan Meuller, Gunilla Kanter-Smoler, Anders O.H. Nygren, Abdellatif Errami, Henrik Grönberg, Eva Holmberg, Jan Björk, Jan Wahlström, Margareta Nordling	20
12	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
13	Spectrum of Mutations in the CFTR Gene of Patients with Classical and Atypical Forms of Cystic Fibrosis from Southwestern Sweden: Identification of 12 Novel Mutations 2001 ·Genetic Testing ·Birgitta Strandvik, (unknown), Marie Fallström, Eva Gronowitz, (unknown), Anders Lindblad, D. Markiewicz, Jan Wahlström, Lap‐Chee Tsui, Julian Zielenski	21
14	Highly Activated T-Cell Receptor AV2S3+ CD4+ Lung T-Cell Expansions in Pulmonary Sarcoidosis 2001 ·American Journal of Respiratory and Critical Care Medicine ·Kianoosh Katchar, Jan Wahlström, Anders Eklúnd, Johan Grünewald	57
15	Analysis of Intracellular Cytokines in CD4+ and CD8+ Lung and Blood T Cells in Sarcoidosis 2001 ·American Journal of Respiratory and Critical Care Medicine ·Jan Wahlström, Kianoosh Katchar, Hans Wigzell, Olle Olerup, Anders Eklúnd, Johan Grünewald	131
16	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
17	Dominant Hereditary Inclusion-Body Myopathy Gene (IBM3) Maps to Chromosome Region 17p13.1 1999 ·The American Journal of Human Genetics ·Tommy Martinsson, Niklas Darín, Mårten Kyllerman, Anders Oldfors, Birgitta Hallberg, Jan Wahlström	33
18	Further studies on a male monozygotic triplet with schizophrenia: cytogenetical and neurobiological assessments in the patients and their parents 1997 ·European Archives of Psychiatry and Clinical Neuroscience ·Erik G. Jönsson, C. Härnryd, (unknown), Jan Wahlström, Johan Bergenius, H. Bergstedt, Dan Greitz, Håkan Nyman, (unknown), Elisabeth Blennow, Göran C. Sedvall	3
19	Rett syndrome—Clinical & biological aspects. 1993 ·Bengt Hagberg, Maria Anvret, Jan Wahlström	13
20	Leber's hereditary optic neuropathy and complex I deficiency in muscle 1991 ·Annals of Neurology ·Nils‐Göran Larsson, Oluf Andersen, Elisabeth Holme, Anders Oldfors, Jan Wahlström	124

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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