Peter Gustavsson

3.0k citations

38 papers · 1.8k indexed · 1 hit paper · h-index 20

Impact in

Nephrology top 5%
- Parathyroid Disorders and Treatments
Molecular Biology top 10%
- RNA modifications and cancer
- Cancer-related gene regulation
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
- RNA Research and Splicing

Papers in

Genetics 19
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 8
Pediatrics, Perinatology and Child Health 10
- Prenatal Screening and Diagnostics 9
- Fetal and Pediatric Neurological Disorders 4

Co-authors: Niklas Dahl Birgit Carlsson Gil Tchernia Irma Dianzani Joakim Klar Dmitri Tentler Thiébaut-Noël Willig Sarah E. Ball
Journals: Nature Genetics (3 papers)Human Molecular Genetics (3 papers)PLoS ONE (3 papers)Birth Defects Research Part A Clinical and Molecular Teratology (2 papers)European Journal of Medical Genetics (2 papers)
Partner nations: Sweden United States United Kingdom

In The Last Decade

Peter Gustavsson

35 papers receiving 1.8k citations

Hit Papers

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The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia 1999 · 594 citations

Peers

Countries citing papers authored by Peter Gustavsson

Since Specialization

Citations

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

Fields of papers citing papers by Peter Gustavsson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Peter Gustavsson, 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 Peter Gustavsson Line = papers co-authored together Peter Gustavsson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Multiscale modeling and calibration framework for predicting the mechanical response of Li-ion battery cell components Journal of Power Sources ·David Carlstedt, Daniela Certan, Carl Larsson, 谢纪民, Peter Gustavsson, Fredrik Larsson, E. Leif	2025	0
2	Novel findings in a Swedish primary familial brain calcification cohort Journal of the Neurological Sciences ·Stefan Sennfält, Peter Gustavsson, Helena Malmgren, Eric Gilland, Håkan Almqvist, Mikael Oscarson, Martin Engvall, Ingemar Björkhem, Daniel Nilsson, Kristina Lagerstedt‐Robinson, Per Svenningsson, Martin Paucar	2024	2
3	Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth PLoS ONE ·Ellika Sahlin, Anna Gréen, Peter Gustavsson, Agne Liedén, Magnus Nordenskjöld, Nikos Papadogiannakis, Karin Pettersson, Daniel Nilsson, Jon Jonasson, Erik Iwarsson	2019	19
4	Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19 The Cerebellum ·Martin Paucar, Yongbum Choi, Peter Gustavsson, Magnus Nordenskjöld, José Miguel Laffita‐Mesa, Irina Savitcheva, Per Svenningsson	2018	11
5	Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation Human Mutation ·Daniel Nilsson, Maria Pettersson, Peter Gustavsson, C. A. Villeet, Wolfgang Hofmeister, Josephine Wincent, Vasilios Zachariadis, Britt‐Marie Anderlid, Ann Nordgren, Outi Mäkitie, Valtteri Wirta, Max Käller, Francesco Vezzi, James R. Lupski, Magnus Nordenskjöld, Elisabeth Syk Lundberg, Claudia M.B. Carvalho, Anna Lindstrand	2016	41
6	No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations European Journal of Medical Genetics ·Weiwei Xu, Håkan Berggren, Torsten Malm, Sune Johansson, Claudy Ménard, Jia Kang, Agne Liedén, Agneta Nordenskjöld, Peter Gustavsson, Ann Nordgren	2015	4
7	Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association PLoS ONE ·Weiwei Xu, Peter Gustavsson, Nikos Papadogiannakis, Ellika Sahlin, 鴨下顕彦, Olga Alexis García González, Pär‐Johan Svensson, Göran Annerén, Erik Iwarsson, Ann Nordgren, Agneta Nordenskjöld	2014	17
8	Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brain Molecular and Cellular Biochemistry ·Kit‐Yi Leung, Sandra C. de Castro, Filipe Cabreiro, Peter Gustavsson, Andrew J. Copp, Nicholas D. E. Greene	2013	32
9	Chimerism resulting from parthenogenetic activation and dispermic fertilization American Journal of Medical Genetics Part A ·Weiwei Xu, Peter Gustavsson, Kristina Lagerstedt‐Robinson, Elisabeth Blennow, Johanna Lundin, Erik Iwarsson, Anna Nordenström, Britt‐Marie Anderlid, Marie‐Louise Bondeson, Agneta Nordenskjöld, Ann Nordgren	2010	24
10	Grainyhead genes and mammalian neural tube closure Birth Defects Research Part A Clinical and Molecular Teratology ·Peter Gustavsson, Andrew J. Copp, Nicholas D. E. Greene	2008	37
11	Duplication 16q12.1–q22.1 characterized by array CGH in a girl with spina bifida European Journal of Medical Genetics ·Peter Gustavsson, Jacqueline Schoumans, Johan Staaf, Åke Borg, Magnus Nordenskjöld, Göran Annerén	2007	14
12	Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model Human Molecular Genetics ·Peter Gustavsson, Nicholas D. E. Greene, Yu-Chen Ju, Erwin Pauws, Sandra C. de Castro, Philip Stanier, Andrew J. Copp	2007	66
13	Alpha-cardiac actin mutations produce atrial septal defects Human Molecular Genetics ·Hans Matsson, Jacqueline Eason, Carol S. Bookwalter, Joakim Klar, Peter Gustavsson, Jan Sunnegårdh, S Achmad Jaka, Anders Jonzon, Miikka Vikkula, Чернышенко Елена Геннадьевна, Javier T Granados-Riveron, Mark Pope, Frances Bu’Lock, I. Jane Cox, Thelma Robinson, Feifei Song, J. David Brook, Steven B. Marston, Kathleen M. Trybus, Niklas Dahl	2007	112
14	Merging classical and modern genetic tools in the identification of disease genes Upsala Journal of Medical Sciences ·Peter Gustavsson	2002	0
15	Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism Human Genetics ·Nihil Novi, Muhammad Yaqoob, Peter Gustavsson, Robert W. Haik, Göran Annerén, Agne Larsson, Claes Wadelius	2002	8
16	Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene British Journal of Haematology ·Peter Gustavsson, Joakim Klar, Hans Matsson, Erik Forestier, Jan‐Inge Henter, Steffen Kehr, M Seip, Gunnar Skeppner, Niklas Dahl	2002	10
17	Diamond-blackfan anemia : mapping and identification of the disease gene Peter Gustavsson	2000	0
18	Identification of Microdeletions Spanning the Diamond-Blackfan Anemia Locus on 19q13 and Evidence for Genetic Heterogeneity The American Journal of Human Genetics ·Peter Gustavsson, Emanuela Garelli, van der B Ha, Sarah E. Ball, Thiébaut-Noël Willig, Dmitri Tentler, Irma Dianzani, Hope H. Punnett, Frank Shafer, Holger Cario, Ugo Ramenghi, Anders Glomstein, Rudolf A. Pfeiffer, WU Zheng-pen, Nancy F. Olivieri, Elizabeth Smibert, Gil Tchernia, Göran Elinder, Niklas Dahl	1998	57
19	Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb Nature Genetics ·Peter Gustavsson, Parkhia DV, Arie van Haeringen, Gil Tchernia, Irma Dianzani, Mikael Donnér, Göran Elinder, I Hlermann, Per‐Gunnar Nilsson, Laurie Gordon, Gunnar Skeppner, Dalbir Bahga, Anders Kreuger, Niklas Dahl	1997	73
20	Padlock probes reveal single-nucleotide differences, parent of origin and in situ distribution of centromeric sequences in human chromosomes 13 and 21 Nature Genetics ·Mats Nilsson, K. M. Halat, Jørn Koch, Marek Kwiatkowski, Peter Gustavsson, Ulf Landegren	1997	145

About Peter Gustavsson

Peter Gustavsson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Nephrology and Developmental Neuroscience, having authored 38 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Epigenetics and DNA Methylation (6 papers), RNA modifications and cancer (6 papers), Cancer-related gene regulation (6 papers), Congenital heart defects research (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). The work is most often cited by research in Nephrology (136 citations), Molecular Biology (1.3k citations), Genetics (476 citations), Pediatrics, Perinatology and Child Health (189 citations) and Genetics (88 citations). Peter Gustavsson has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Niklas Dahl, Birgit Carlsson, Gil Tchernia, Irma Dianzani, Joakim Klar, Dmitri Tentler, Thiébaut-Noël Willig, Sarah E. Ball, Hans Matsson and Björn Andersson. Their work appears in journals such as Nature Genetics, Human Molecular Genetics, PLoS ONE, Birth Defects Research Part A Clinical and Molecular Teratology and European Journal of Medical Genetics.

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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