J. Wahlström

3.6k total citations
91 papers, 2.6k citations indexed

About

J. Wahlström is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, J. Wahlström has authored 91 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 24 papers in Molecular Biology and 18 papers in Physiology. Recurrent topics in J. Wahlström's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (11 papers) and Genetics and Neurodevelopmental Disorders (10 papers). J. Wahlström is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (11 papers) and Genetics and Neurodevelopmental Disorders (10 papers). J. Wahlström collaborates with scholars based in Sweden, United States and Norway. J. Wahlström's co-authors include Tommy Martinsson, Johan Grünewald, Anders Eklúnd, Annica Inerot, G Swanbeck, Fredrik Enlund, Charlotta Enerbäck, Maria Yhr, Anders Oldfors and Lena Samuelsson and has published in prestigious journals such as The Lancet, Brain and Neurology.

In The Last Decade

J. Wahlström

88 papers receiving 2.5k citations

Peers

Countries citing papers authored by J. Wahlström

Since Specialization

Citations

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

Fields of papers citing papers by J. Wahlström

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Wahlström

This figure shows the co-authorship network connecting the top 25 collaborators of J. Wahlström. A scholar is included among the top collaborators of J. 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 J. Wahlström. J. 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	Increased intraepithelial (CD103+) CD8+ T cells in the airways of smokers with and without chronic obstructive pulmonary disease 2012 ·Immunobiology ·(unknown), Helena Forsslund, Liwei Cui, Johan Grünewald, Åsa M. Wheelock, J. Wahlström, C. Magnus Sköld	25
2	Are variations in length of Y chromosome due to structural changes? 2009 ·Hereditas ·J. Wahlström	1
3	Identification by fluorescence of apparently extra human F chromosomes as G chromosomes with giant satellites 2009 ·Hereditas ·J. Wahlström	0
4	An Uneven Expression of T Cell Receptor V Genes in the Arterial Wall and Peripheral Blood in Giant Cell Arteritis 2008 ·Inflammation ·C. Schaufelberger, Rune Andersson, Elisabeth Nordborg, Göran K. Hansson, Claes Nordborg, J. Wahlström	11
5	Replication error, a new hypothesis to explain the origin of a supernumerary marker chromosome in a mentally retarded boy 2008 ·Hereditas ·(unknown), (unknown), J. Wahlström, Ulrika von Döbeln, R Olegård	1
6	Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32 2007 ·Tissue Antigens ·Svetlana Adamovic, Silja Svanstrøm Amundsen, Benedicte A. Lie, Åsa Hellqvist, Audur H. Gudjónsdóttir, J. Ek, Staffan Nilsson, J. Wahlström, Henry Ascher, Ludvig M. Sollid, Åsa Torinsson Naluai	8
7	Novel Findings in Swedish Patients With MYH-Associated Polyposis: Mutation Detection and Clinical Characterization 2006 ·Clinical Gastroenterology and Hepatology ·Gunilla Kanter-Smoler, Jan Björk, (unknown), Yvonne Engwall, Birgitta Hallberg, Göran Karlsson, Henrik Grönberg, Per Karlsson, Arne Wallgren, J. Wahlström, (unknown), (unknown)	22
8	Phenotypic analysis of alveolar macrophages and lymphocytes following allergen inhalation by atopic subjects with mild asthma 2005 ·Respiratory Medicine ·(unknown), Kianoosh Katchar, Anders Eklúnd, Johan Grünewald, J. Wahlström	23
9	Genetic analysis of the CD28/CTLA4/ICOS (CELIAC3) region in coeliac disease 2004 ·Tissue Antigens ·Silja Svanstrøm Amundsen, Åsa Torinsson Naluai, Henry Ascher, J. Ek, Audur H. Gudjónsdóttir, J. Wahlström, Benedicte A. Lie, Ludvig M. Sollid	39
10	T Cell Receptor Vβ Expression in Patients with Allergic Asthma before and after Repeated Low-Dose Allergen Inhalation 2001 ·Clinical Immunology ·J. Wahlström, Dulceaydee Gigliotti, A. Roquet, Hans Wigzell, Anders Eklúnd, Johan Grünewald	9
11	Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles 1998 ·Annals of Neurology ·Niklas Darín, Mårten Kyllerman, J. Wahlström, Tommy Martinsson, Anders Oldfors	62
12	Lung and blood T-cell receptor repertoire in extrinsic allergic alveolitis 1997 ·European Respiratory Journal ·J. Wahlström, M Berlin, Rune Lundgren, Olle Olerup, Hans Wigzell, Anders Eklúnd, Johan Grünewald	43
13	Boy with a ring 7 chromosome: a case report with special reference to dermatological findings 1996 ·Acta Paediatrica ·J. Wahlström, Ragnar Bjarnason, Inger Rosdahl, Kerstin Albertsson‐Wikland	15
14	The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q 1994 ·Clinical Genetics ·J. Wahlström, Laurie J. Ozelius, P. L. Kramer, (unknown), Deborah E. Schuback, Lars Forsgren, Gösta Holmgren, Ulf Drugge, Gunnar Sanner, Stanley Fahn, X. O. Breakefield	11
15	Frequency of four cystic fibrosis mutations in a Swedish population 1993 ·Acta Paediatrica ·Niklas Dahl, Ulla Grandell, Tommy Martinsson, Marie Allen, Lena Johansson, (unknown), (unknown), Lena Hjelte, H Kollberg, Birgitta Strandvik, J. Wahlström, Maria Anvret	7
16	Silver‐like syndrome and a small deletion on chromosome 13 1993 ·Acta Paediatrica ·J. Wahlström, Gösta Holmgren, Kerstin Albertsson‐Wikland, Carl‐Johan Törnhage	3
17	Chromosomes in Anorexia Nervosa. A Study of 47 Cases Including a Population‐Based Group: A Research Note 1991 ·Journal of Child Psychology and Psychiatry ·Maria Råstam, Christopher Gillberg, J. Wahlström	6
18	Gene map of mental retardation 1990 ·Journal of Intellectual Disability Research ·J. Wahlström	16
19	First‐trimester diagnosis of juvenile neuronal ceroid lipofuscinosis by demonstration of fingerprint inclusions in chorionic villi 1989 ·Prenatal Diagnosis ·Nils Conradi, Paul Uvebrant, (unknown), J. Wahlström, (unknown)	27
20	[Risk of miscarriage after chorionic biopsy is probably not higher than after amniocentesis]. 1989 ·PubMed ·Björn Gustavii, (unknown), Ulf Kristoffersson, Joachim Mark, (unknown), (unknown), J. Wahlström, (unknown), (unknown), Therése Andersson	2

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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