Maritta Hellström Pigg

729 total citations
19 papers, 369 citations indexed

About

Maritta Hellström Pigg is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Maritta Hellström Pigg has authored 19 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Cell Biology and 6 papers in Genetics. Recurrent topics in Maritta Hellström Pigg's work include Skin and Cellular Biology Research (10 papers), Dermatological and Skeletal Disorders (5 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Maritta Hellström Pigg is often cited by papers focused on Skin and Cellular Biology Research (10 papers), Dermatological and Skeletal Disorders (5 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Maritta Hellström Pigg collaborates with scholars based in Sweden, Germany and Norway. Maritta Hellström Pigg's co-authors include Agneta Gånemo, Niklas Dahl, Britta Berglund, Per Kristiansson, Ingrid Haußer, Anders Vahlquist, Marie Virtanen, Tobias Gedde‐Dahl, I. Anton‐Lamprecht and Claes Wadelius and has published in prestigious journals such as Nature Genetics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Maritta Hellström Pigg

18 papers receiving 359 citations

Peers

Countries citing papers authored by Maritta Hellström Pigg

Since Specialization

Citations

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

Fields of papers citing papers by Maritta Hellström Pigg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maritta Hellström Pigg. 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 Maritta Hellström Pigg. The network helps show where Maritta Hellström Pigg may publish in the future.

Co-authorship network of co-authors of Maritta Hellström Pigg

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Genotypic and Phenotypic Characterization of Seven Individuals With Predicted Bone Morphogenetic Protein 2 ( BMP2 ) Haploinsufficiency 2025 ·Clinical Genetics ·(unknown), Anna Hammarsjö, Anna Lindstrand, Ann Nordgren, Giedré Grigelioniené, Maritta Hellström Pigg	0
2	A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population 2022 ·PLoS ONE ·Kristina Lagerstedt‐Robinson, Izabella Baranowska Körberg, (unknown), Erik Björck, Emma Tham, (unknown), Maritta Hellström Pigg, Ylva Paulsson-Karlsson, Magnus Nordenskjöld, Maria Soller, (unknown)	6
3	Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26 2017 ·Human Molecular Genetics ·Sanna Gudmundsson, Maria Wilbe, Sara Ekvall, Adam Ameur, Nicola Cahill, Ludmil B. Alexandrov, Marie Virtanen, Maritta Hellström Pigg, Anders Vahlquist, Hans Törmä, Marie-Louise Bondeson	23
4	Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients 2016 ·Acta Dermato Venereologica ·Maritta Hellström Pigg, Anette Bygum, Agneta Gånemo, Marie Virtanen, F Brandrup, Andreas Zimmer, Alrun Hotz, A. Vahlquist, Johannes Fischer	55
5	Drug‐Mediated Gene Regulation of Vitamin D₃ Metabolism in Primary Human Dermal Fibroblasts 2016 ·Basic & Clinical Pharmacology & Toxicology ·Maria Norlin, Johan Lundqvist, Maria Ellfolk, Maritta Hellström Pigg, Jan Gustafsson, Kjell Wikvall	9
6	Self-reported quality of life, anxiety and depression in individuals with Ehlers-Danlos syndrome (EDS): a questionnaire study 2015 ·BMC Musculoskeletal Disorders ·Britta Berglund, (unknown), Maritta Hellström Pigg, Per Kristiansson	56
7	Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda 2014 ·Acta Dermato Venereologica ·(unknown), Anders Vahlquist, Marianna Virtanen, (unknown), Lisbet K. Lind, Anita Lundström, Maritta Hellström Pigg	14
8	Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis 2007 ·Journal of Medical Genetics ·Johanna Dahlqvist, Joakim Klar, Ingrid Haußer, I. Anton‐Lamprecht, Maritta Hellström Pigg, Tobias Gedde‐Dahl, Agneta Gånemo, Anders Vahlquist, Niklas Dahl	45
9	Fatal Bleeding following Delivery: A Manifestation of the Vascular Type of Ehlers-Danlos’ Syndrome 2006 ·Gynecologic and Obstetric Investigation ·Martin Björck, Maritta Hellström Pigg, Björn Kragsterman, (unknown)	10
10	A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association 2006 ·Journal of Human Genetics ·Malin Melin, Joakim Klar, (unknown), Robert Fredriksson, Ingrid Haußer, F Brandrup, Anette Bygum, A. Vahlquist, Maritta Hellström Pigg, Niklas Dahl	15
11	Detailed Genetic and Physical Mapping in the Sjögren-Larsson Syndrome Gene Region in 17p11.2 2004 ·Hereditas ·Anna Sillén, Anders Alderborn, Maritta Hellström Pigg, Sten Jagell, Claes Wadelius	4
12	The Clinical Spectrum of Congenital Ichthyosis in Sweden: A Review of 127 Cases 2003 ·Acta Dermato Venereologica ·Anders Vahlquist, Agneta Gånemo, Maritta Hellström Pigg, Marie Virtanen, Per Westermark	22
13	Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosis 2000 ·Prenatal Diagnosis ·Maritta Hellström Pigg, Tobias Gedde‐Dahl, Diane W. Cox, Guttorm Haugen, Niklas Dahl	7
14	Further Evidence of Genetic Homogeneity in Sj gren-Larsson Syndrome 1999 ·Acta Dermato Venereologica ·Maritta Hellström Pigg	3
15	Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway 1998 ·European Journal of Human Genetics ·Maritta Hellström Pigg, Tobias Gedde‐Dahl, Diane W. Cox, Ingrid Haußer, I. Anton‐Lamprecht, Niklas Dahl	42
16	Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatellite. 1995 ·PubMed ·(unknown), Maritta Hellström Pigg, (unknown), (unknown), (unknown), Ed J. Kuijper, C. C. Tijssen, (unknown), K. H. Gustavson, (unknown)	2
17	The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association 1994 ·Nature Genetics ·Maritta Hellström Pigg, Sten Jagell, Anna Sillén, Jean Weissenbach, Karl‐Henrik Gustavson, Claes Wadelius	33
18	Hemophilia B in a 46,XX female probably caused by non‐random X inactivation 1993 ·Clinical Genetics ·Claes Wadelius, (unknown), Maritta Hellström Pigg, Nils Egberg, Ulf Pettersson, Maria Anvret	17
19	Linkage analysis in properdin deficiency families: refined location in proximal Xp 1992 ·Clinical Genetics ·Claes Wadelius, Maritta Hellström Pigg, Mats Sundvall, Anders G. Sjöholm, P. Goonewardena, Ed J. Kuijper, Cees Tijssen, (unknown), Peter Späth, (unknown), Lisbeth Tranebjærg, Hans Erik Nielsen, (unknown), Göran Annerén, Ulf Pettersson	6

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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