H Malmgren

762 total citations
16 papers, 565 citations indexed

About

H Malmgren is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H Malmgren has authored 16 papers receiving a total of 565 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in H Malmgren's work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (5 papers). H Malmgren is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (5 papers). H Malmgren collaborates with scholars based in Sweden, France and Hong Kong. H Malmgren's co-authors include Niklas Dahl, Dominique Heitz, Jack Tarleton, Angela Barnicoat, Christopher G. Mathew, Étienne Mornet, Isabel Tejada, Janet L. Macpherson, François Rousseau and U. Pettersson and has published in prestigious journals such as Genome Research, Human Reproduction and Genomics.

In The Last Decade

H Malmgren

16 papers receiving 556 citations

Peers

H Malmgren

GENET

PPCH

J. Herbergs Netherlands

G. Glóver Spain

Vikram Jaswaney United States

C.E. Browne United Kingdom

Brian P. Perry United States

Damina Balmer Switzerland

Stuart Purvis‐Smith Australia

I. López Spain

Marie‐Françoise Croquette France

Peter M. Kroisel Austria

J. Herbergs Netherlands

H Malmgren

405 ×0.9

GENET

321 ×1.1

127 ×0.7

113 ×1.0

PPCH

68 ×1.2

Citations per year, relative to H Malmgren H Malmgren (= 1×) peers J. Herbergs

Countries citing papers authored by H Malmgren

Since Specialization

Citations

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

Fields of papers citing papers by H Malmgren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Malmgren

This figure shows the co-authorship network connecting the top 25 collaborators of H Malmgren. A scholar is included among the top collaborators of H 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 H Malmgren. H 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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16 of 16 papers shown

Kakourou, Georgia, Semra Kahraman, Georgia Kourlaba, et al.. (2017). The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study. Human Reproduction. 33(3). 520–530. 18 indexed citations

Malmgren, H, et al.. (2012). One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre. Human Reproduction. 27(9). 2843–2849. 12 indexed citations

Lindstrand, Anna, et al.. (2010). Improved structural characterization of chromosomal breakpoints using high resolution custom array‐CGH. Clinical Genetics. 77(6). 552–562. 8 indexed citations

Iwarsson, Erik, H Malmgren, & Elisabeth Blennow. (2010). Preimplantation genetic diagnosis: twenty years of practice. Seminars in Fetal and Neonatal Medicine. 16(2). 74–80. 12 indexed citations

Lindstrand, Anna, H Malmgren, Sigrid Sahlén, et al.. (2009). Detailed molecular and clinical characterization of three patients with 21q deletions. Clinical Genetics. 77(2). 145–154. 52 indexed citations

Blennow, Elisabeth, et al.. (2008). Concurrent microdeletion and duplication of 22q11.2. Clinical Genetics. 74(1). 61–67. 11 indexed citations

Lindstrand, Anna, H Malmgren, Sigrid Sahlén, et al.. (2008). Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletion. American Journal of Medical Genetics Part A. 146A(24). 3217–3222. 8 indexed citations

Malmgren, H. (2006). PGD for dystrophin gene deletions using fluorescence in situ hybridization. Molecular Human Reproduction. 12(5). 353–356. 8 indexed citations

Malmgren, H, Gunilla Malm, Sigrid Sahlén, Markus Karlsson, & Elisabeth Blennow. (2005). Molecular cytogenetic characterization of an insertional translocation, ins(6;7)(p25;q33q34): Deletion/duplication of 7q33‐34 and clinical correlations. American Journal of Medical Genetics Part A. 139A(1). 25–31. 5 indexed citations

10.

Malmgren, H. (2002). Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrations. Molecular Human Reproduction. 8(5). 502–510. 50 indexed citations

11.

Malmgren, H, Sigrid Sahlén, José Inzunza, et al.. (2002). O-12. Single-cell comparative genomic hybridization analysis of human preimplantation embryos from patients with balanced structural chromosome aberrations undergoing PGD. Reproductive BioMedicine Online. 4. 14–15. 2 indexed citations

12.

Rousseau, François, Dominique Heitz, Jack Tarleton, et al.. (1994). A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.. PubMed. 55(2). 225–37. 238 indexed citations

13.

Malmgren, H, Mats Sundvall, Niklas Dahl, et al.. (1993). Linkage mapping of a severe X-linked mental retardation syndrome.. PubMed. 52(6). 1046–52. 26 indexed citations

14.

Malmgren, H, et al.. (1991). Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA.. Genome Research. 1(2). 111–119. 62 indexed citations

15.

Vincent, Anne, Niklas Dahl, I. Oberlé, et al.. (1989). The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus. Genomics. 5(4). 797–801. 19 indexed citations

16.

Dahl, Niklas, P. Goonewardena, H Malmgren, et al.. (1989). Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).. PubMed. 45(2). 304–9. 34 indexed citations

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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