Helena Malmgren

3.3k total citations · 1 hit paper
42 papers, 1.4k citations indexed

About

Helena Malmgren is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Helena Malmgren has authored 42 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 22 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Helena Malmgren's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Helena Malmgren is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Helena Malmgren collaborates with scholars based in Sweden, United States and France. Helena Malmgren's co-authors include Ulf Landegren, Mats Nilsson, Marek Kwiatkowski, Martina Samiotaki, Bhanu P. Chowdhary, Niklas Dahl, Ann Nordgren, Elisabeth Blennow, Ulf Pettersson and Anna Lindstrand and has published in prestigious journals such as Science, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Helena Malmgren

41 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.

Padlock Probes: Circularizing Oligonucleotides for Localized DNA Detection

1994 582 citations Helena Malmgren, Ulf Landegren et al. profile →

Peers

Countries citing papers authored by Helena Malmgren

Since Specialization

Citations

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

Fields of papers citing papers by Helena Malmgren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helena Malmgren

This figure shows the co-authorship network connecting the top 25 collaborators of Helena Malmgren. A scholar is included among the top collaborators of Helena Malmgren 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 Helena Malmgren. Helena Malmgren 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	Genome sequencing in a cohort of 32 fetuses with genetic skeletal disorders 2025 ·European Journal of Human Genetics ·(unknown), Anna Hammarsjö, (unknown), (unknown), Peter Conner, Nikos Papadogiannakis, (unknown), Laura Orellana, Malin Kvarnung, Helena Malmgren, Kristina Lagerstedt‐Robinson, Ann Nordgren, Anna Lindstrand, Gen Nishimura, Giedré Grigelioniené	1
2	SPNS1 variants cause multiorgan disease and implicate lysophospholipid transport as critical for mTOR-regulated lipid homeostasis 2025 ·Journal of Clinical Investigation ·(unknown), Mei Ding, Michaela Chocholoušková, Cheen Fei Chin, Martin Engvall, Helena Malmgren, Matias Wagner, Marlen C. Lauffer, (unknown), May Christine V. Malicdan, Valérie Allamand, Madeleine Durbeej, A M Delgado-Vega, Thomas Sejersen, Ann Nordgren, Federico Torta, David L. Silver	1
3	TP53 p.R181H is enriched in the Swedish cohort (SWEP53) and associated with a distinct breast and prostate phenotype 2025 ·Scientific Reports ·(unknown), (unknown), (unknown), Helena Malmgren, (unknown), Susana Seixas, Carla Oliveíra, Emma Tham, Svetlana Bajalica‐Lagercrantz	0
4	Genome sequencing differentiates a paracentric inversion from a balanced insertion enabling more accurate preimplantation genetic testing 2024 ·Acta Obstetricia Et Gynecologica Scandinavica ·Josephine Wincent, Hafdís T. Helgadóttir, (unknown), (unknown), Claudia M.B. Carvalho, Helena Malmgren, Anna Lindstrand, Erik Iwarsson	1
5	Novel findings in a Swedish primary familial brain calcification cohort 2024 ·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	2
6	Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders 2023 ·Frontiers in Neurology ·(unknown), Daniel Nilsson, Martin Engvall, Helena Malmgren, Håkan Thonberg, Maria Pettersson, Britt‐Marie Anderlid, Anna Hammarsjö, Hafdís T. Helgadóttir, Snjólaug Arnardottir, K Naess, Inger Nennesmo, Martin Paucar, (unknown), Rayomand Press, Göran Solders, Thomas Sejersen, Anna Lindstrand, Malin Kvarnung	4
7	Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants 2022 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), Tobias Laurell, Anna Lindstrand, (unknown), Helena Malmgren, Kristina Lagerstedt‐Robinson, Bianca Tesi, Fulya Taylan, Ann Nordgren	10
8	Biallelic mutations in WRAP53 result in dysfunctional telomeres, Cajal bodies and DNA repair, thereby causing Hoyeraal–Hreidarsson syndrome 2020 ·Cell Death and Disease ·(unknown), Stefanie Böhm, Helena Malmgren, Anna Norberg, Mikael Sundin, Ann Nordgren, Marianne Farnebo	22
9	The cerebellar phenotype of Charcot-Marie-Tooth neuropathy type 4C 2019 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Kristin Samuelsson, (unknown), Per Svenningsson, Helena Malmgren, (unknown), Alberto J. Espay, Rayomand Press, Göran Solders, Martin Paucar	9
10	A novel approach using long‐read sequencing and ddPCR to investigate gonadal mosaicism and estimate recurrence risk in two families with developmental disorders 2017 ·Prenatal Diagnosis ·Maria Wilbe, Sanna Gudmundsson, (unknown), Adam Ameur, Eva‐Lena Stattin, Göran Annerén, Helena Malmgren, Carina Frykholm, Marie‐Louise Bondeson	20
11	Small mosaic deletion encompassing the snoRNAs and SNURF‐SNRPN results in an atypical Prader–Willi syndrome phenotype 2013 ·American Journal of Medical Genetics Part A ·Britt‐Marie Anderlid, (unknown), Helena Malmgren, Mikael Lehtihet, Ann Nordgren	21
12	GSTM1 Gene Expression Correlates to Leiomyoma Volume Regression in Response to Mifepristone Treatment 2013 ·PLoS ONE ·(unknown), (unknown), Kristina Lagerstedt‐Robinson, Helena Malmgren, Anna Hammarsjö, Birgitta Byström, Parameswaran Grace Lalitkumar, Kristina Gemzell‐Danielsson	24
13	In Vivo Differentiated Human Embryonic Stem Cells Can Acquire Chromosomal Aberrations More Frequently Than In Vitro During the Same Period 2012 ·Stem Cells and Development ·Marco Zucchelli, Susanne Ström, Frida Holm, Helena Malmgren, Sigrid Sahlén, Piotr Religa, Outi Hovatta, Juha Kere, José Inzunza	5
14	Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities 2009 ·Pediatric Blood & Cancer ·Göran Carlsson, Göran Elinder, Helena Malmgren, Alicja Trębińska, Ewa A. Grzybowska, Niklas Dahl, Magnus Nordenskjöld, Bengt Fadeel	10
15	Distal 3p deletion syndrome: Detailed molecular cytogenetic and clinical characterization of three small distal deletions and review 2007 ·American Journal of Medical Genetics Part A ·Helena Malmgren, Sigrid Sahlén, Katarina Wide, (unknown), Elisabeth Blennow	46
16	Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities 2001 ·Prenatal Diagnosis ·Margareta Fridström, Lars Ährlund‐Richter, Erik Iwarsson, Helena Malmgren, José Inzunza, Björn Rosenlund, Peter Sjöblom, Magnus Nordenskjöld, Elisabeth Blennow, Outi Hovatta	25
17	Presence of an IDS-Related Locus(IDS2) in Xq28 Complicates theMutational Analysis of HunterSyndrome 1995 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Helena Malmgren, Niklas Dahl	41
18	Inversion of the IDS gene resulting from recombination with IDS-related sequences in a common cause of the Hunter syndrome 1995 ·Human Molecular Genetics ·(unknown), Niklas Dahl, Helena Malmgren, Wim J. Kleijer, T. Tønnesen, (unknown), Ulf Pettersson	120
19	1.5-Mb YAC Contig in Xq28 Formatted with Sequence-Tagged Sites and Including a Region Unstable in the Clones 1993 ·Genomics ·Giuseppe Palmieri, Giovanna Romano, Amelia Casamassimi, Michele D’Urso, Randall D. Little, Fatima Abidi, David Schlessinger, (unknown), Helena Malmgren, (unknown), Ulf Pettersson, Ulf Landegren	12
20	New X‐linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death 1993 ·American Journal of Medical Genetics ·Karl‐Henrik Gustavson, Göran Annerén, Helena Malmgren, Niklas Dahl, (unknown), (unknown)	24

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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