Øyvind Helgeland

4.2k total citations
16 papers, 302 citations indexed

About

Øyvind Helgeland is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Øyvind Helgeland has authored 16 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Øyvind Helgeland's work include Genetic Associations and Epidemiology (7 papers), Pregnancy and preeclampsia studies (2 papers) and Genomics and Rare Diseases (2 papers). Øyvind Helgeland is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Pregnancy and preeclampsia studies (2 papers) and Genomics and Rare Diseases (2 papers). Øyvind Helgeland collaborates with scholars based in Norway, Sweden and United Kingdom. Øyvind Helgeland's co-authors include Stefan Johansson, Pål R. Njølstad, Bo Jacobsson, Marc Vaudel, Jonas Bačelis, Gun Peggy Knudsen, Louis J. Muglia, Mikko Hallman, Ronny Myhre and Ge Zhang and has published in prestigious journals such as Nature Communications, Bioinformatics and Human Molecular Genetics.

In The Last Decade

Øyvind Helgeland

15 papers receiving 301 citations

Peers

Øyvind Helgeland

GENET

PPCH

PHEOH

Carmen Mazza Argentina

Marianne Becker Germany

Sowmya Krishnan United States

Alexandra C. Gillett United Kingdom

Chunxiao Liao China

Natalya Zymak‐Zakutnya Ukraine

Sine Knorr Denmark

Toby Candler United Kingdom

Katharine F. Hunt United Kingdom

Carmen Mazza Argentina

Øyvind Helgeland

193 ×1.4

GENET

104 ×0.8

PPCH

57 ×0.9

18 ×0.3

54 ×1.3

PHEOH

Citations per year, relative to Øyvind Helgeland Øyvind Helgeland (= 1×) peers Carmen Mazza

Countries citing papers authored by Øyvind Helgeland

Since Specialization

Citations

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

Fields of papers citing papers by Øyvind Helgeland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Øyvind Helgeland

This figure shows the co-authorship network connecting the top 25 collaborators of Øyvind Helgeland. A scholar is included among the top collaborators of Øyvind Helgeland 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 Øyvind Helgeland. Øyvind Helgeland 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

Qu, Hui‐Qi, John J. Connolly, Peter Kraft, et al.. (2023). Trans‐ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium study. Clinical and Translational Medicine. 13(6). e1291–e1291. 3 indexed citations

Helgeland, Øyvind, Marc Vaudel, Pol Solé-Navais, et al.. (2022). Characterization of the genetic architecture of infant and early childhood body mass index. Nature Metabolism. 4(3). 344–358. 30 indexed citations

Hughes, Amanda, Eleanor Sanderson, Tim Morris, et al.. (2022). Body mass index and childhood symptoms of depression, anxiety, and attention-deficit hyperactivity disorder: A within-family Mendelian randomization study. eLife. 11. 7 indexed citations

Lavrichenko, Ksenia, Øyvind Helgeland, Pål R. Njølstad, Inge Jonassen, & Stefan Johansson. (2021). SeeCiTe: a method to assess CNV calls from SNP arrays using trio data. Bioinformatics. 37(13). 1876–1883. 3 indexed citations

Flatley, Christopher, Pol Solé-Navais, Marc Vaudel, et al.. (2021). Placental weight centiles adjusted for age, parity and fetal sex. Placenta. 117. 87–94. 24 indexed citations

Romanowska, Julia, et al.. (2021). A fast wavelet-based functional association analysis replicates several susceptibility loci for birth weight in a Norwegian population. BMC Genomics. 22(1). 321–321.

Hannigan, Laurie J., Ragna Bugge Askeland, Helga Ask, et al.. (2020). Genetic Liability for Schizophrenia and Childhood Psychopathology in the General Population. Schizophrenia Bulletin. 47(4). 1179–1189. 9 indexed citations

Solé-Navais, Pol, Jonas Bačelis, Øyvind Helgeland, et al.. (2020). Autozygosity mapping and time-to-spontaneous delivery in Norwegian parent-offspring trios. Human Molecular Genetics. 29(23). 3845–3858. 1 indexed citations

Lavrichenko, Ksenia, Siren Berland, Øyvind Helgeland, et al.. (2020). Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents. European Journal of Human Genetics. 29(1). 205–215. 44 indexed citations

10.

Ask, Helga, Ted Reichborn‐Kjennerud, Ole A. Andreassen, et al.. (2020). OP96 The causal effect of BMI on neurodevelopment: a within family mendelian randomization study using MoBa. Oral Presentations. A44.2–A45. 1 indexed citations

11.

Helgeland, Øyvind, Marc Vaudel, Pétur Benedikt Júlíusson, et al.. (2019). Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. Nature Communications. 10(1). 4448–4448. 49 indexed citations

12.

Qiao, Zhen, Jie Zheng, Øyvind Helgeland, et al.. (2019). Introducing M-GCTA a Software Package to Estimate Maternal (or Paternal) Genetic Effects on Offspring Phenotypes. Behavior Genetics. 50(1). 51–66. 16 indexed citations

13.

Ding, Yunpeng, Eva Ringdal Pedersen, Gard Frodahl Tveitevåg Svingen, et al.. (2016). Methylenetetrahydrofolate Dehydrogenase 1 Polymorphisms Modify the Associations of Plasma Glycine and Serine With Risk of Acute Myocardial Infarction in Patients With Stable Angina Pectoris in WENBIT (Western Norway B Vitamin Intervention Trial). Circulation Cardiovascular Genetics. 9(6). 541–547. 5 indexed citations

14.

Ding, Yunpeng, Stefan Johansson, Jesse F. Gregory, et al.. (2015). B vitamin treatments modify the risk of myocardial infarction associated with a MTHFD1 polymorphism in patients with stable angina pectoris. Nutrition Metabolism and Cardiovascular Diseases. 26(6). 495–501. 9 indexed citations

15.

Zhang, Ge, Jonas Bačelis, Kari Teramo, et al.. (2015). Assessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization Analysis. PLoS Medicine. 12(8). e1001865–e1001865. 93 indexed citations

16.

Helgeland, Øyvind, Jens Kristoffer Hertel, Anders Molven, et al.. (2015). The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey). International Journal of Endocrinology. 2015. 1–9. 8 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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