Helle Lybæk

751 total citations
15 papers, 282 citations indexed

About

Helle Lybæk is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Helle Lybæk has authored 15 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Helle Lybæk's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Helle Lybæk is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Helle Lybæk collaborates with scholars based in Norway, Netherlands and Australia. Helle Lybæk's co-authors include Gunnar Houge, Gro Oddveig Ness, Jarle B. Arnes, Eyvind Rødahl, Nina Øyen, Vidar M. Steen, Randi Hovland, Trine Prescott, C. T. Stansberg and Karen Helene Ørstavik and has published in prestigious journals such as European Journal of Human Genetics, Journal of Neuro-Oncology and American Journal of Medical Genetics.

In The Last Decade

Helle Lybæk

15 papers receiving 248 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Helle Lybæk Norway 10 162 114 47 44 32 15 282
Eva‐Christina Prott Germany 7 199 1.2× 160 1.4× 27 0.6× 96 2.2× 24 0.8× 9 283
Chad Haldeman‐Englert United States 11 204 1.3× 184 1.6× 42 0.9× 50 1.1× 15 0.5× 21 359
Sonia Nizard France 10 227 1.4× 131 1.1× 21 0.4× 87 2.0× 36 1.1× 12 357
Liesbeth Backx Belgium 10 196 1.2× 183 1.6× 50 1.1× 34 0.8× 7 0.2× 14 333
Yukiko Kuroda Japan 11 178 1.1× 127 1.1× 18 0.4× 31 0.7× 17 0.5× 40 271
Emma Hobson United Kingdom 9 256 1.6× 213 1.9× 37 0.8× 40 0.9× 42 1.3× 24 405
Maria Luigia Cavaliere Italy 13 171 1.1× 257 2.3× 20 0.4× 38 0.9× 28 0.9× 19 372
Robert Maiwald Germany 8 214 1.3× 253 2.2× 19 0.4× 30 0.7× 35 1.1× 13 460
Kelly E. Jackson United States 8 211 1.3× 204 1.8× 40 0.9× 50 1.1× 9 0.3× 15 375
Mónica Rosello Spain 14 360 2.2× 295 2.6× 47 1.0× 95 2.2× 27 0.8× 41 535

Countries citing papers authored by Helle Lybæk

Since Specialization
Citations

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

Fields of papers citing papers by Helle Lybæk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helle Lybæk

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

All Works

15 of 15 papers shown
1.
Lybæk, Helle, Michael I. Robson, Nicole de Leeuw, et al.. (2022). LRFN5 locus structure is associated with autism and influenced by the sex of the individual and locus conversions. Autism Research. 15(3). 421–433. 7 indexed citations
2.
Lybæk, Helle, et al.. (2013). RevSex duplication-induced and sex-related differences in theSOX9regulatory region chromatin landscape in human fibroblasts. Epigenetics. 9(3). 416–427. 14 indexed citations
3.
Griswold, Anthony J., Deqiong Ma, Stephanie Sacharow, et al.. (2011). A de novo 1.5 Mb microdeletion on chromosome 14q23.2‐23.3 in a patient with autism and spherocytosis. Autism Research. 4(3). 221–227. 24 indexed citations
4.
Bruijn, Diederik R.H. de, Rolph Pfundt, Alexander Hoischen, et al.. (2010). Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of <i>LRFN5</i> Expression. Molecular Syndromology. 1(1). 46–57. 30 indexed citations
5.
Misceo, Doriana, Karen Helene Ørstavik, Helle Lybæk, et al.. (2009). Inheritance of a terminal 7.1 Mb 18p deletion flanked by a 2.3 Mb duplication from a physically normal mother. American Journal of Medical Genetics Part A. 149A(12). 2877–2881. 4 indexed citations
6.
Houge, Gunnar, Helle Lybæk, & Sasha Gulati. (2009). Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: A result of failed tetraploidy correction?. BMC Medical Genetics. 10(1). 42–42. 2 indexed citations
7.
8.
Aarhus, Mads, Ove Bruland, Geir Bredholt, et al.. (2008). Microarray analysis reveals down-regulation of the tumour suppressor gene WWOX and up-regulation of the oncogene TYMS in intracranial sporadic meningiomas. Journal of Neuro-Oncology. 88(3). 251–259. 18 indexed citations
9.
10.
Lybæk, Helle, et al.. (2008). Array-CGH fine mapping of minor and cryptic HR-CGH detected genomic imbalances in 80 out of 590 patients with abnormal development. European Journal of Human Genetics. 16(11). 1318–1328. 11 indexed citations
11.
Houge, Gunnar, Helge Boman, Helle Lybæk, Gro Oddveig Ness, & Pétur Benedikt Júlíusson. (2006). Lack of meiotic crossovers during oogenesis in an apparent 45,X Ullrich–Turner syndrome patient with three children. American Journal of Medical Genetics Part A. 140A(10). 1092–1097. 1 indexed citations
12.
Rødahl, Eyvind, Helle Lybæk, Jarle B. Arnes, & Gro Oddveig Ness. (2005). Chromosomal imbalances in some benign orbital tumours. Acta Ophthalmologica Scandinavica. 83(3). 385–391. 15 indexed citations
13.
Ness, Gro Oddveig, Helle Lybæk, Jarle B. Arnes, & Eyvind Rødahl. (2005). Chromosomal imbalances in a recurrent solitary fibrous tumor of the orbit. Cancer Genetics and Cytogenetics. 162(1). 38–44. 21 indexed citations
14.
Ness, Gro Oddveig, Helle Lybæk, & Gunnar Houge. (2002). Usefulness of high‐resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities. American Journal of Medical Genetics. 113(2). 125–136. 55 indexed citations
15.
Ness, Gro Oddveig, Helle Lybæk, Jarle B. Arnes, & Eyvind Rødahl. (2002). Chromosomal imbalances in lymphoid tumors of the orbit.. PubMed. 43(1). 9–14. 9 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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