Thue Bryndorf

1.4k total citations
29 papers, 997 citations indexed

About

Thue Bryndorf is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Plant Science. According to data from OpenAlex, Thue Bryndorf has authored 29 papers receiving a total of 997 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Pediatrics, Perinatology and Child Health, 20 papers in Genetics and 14 papers in Plant Science. Recurrent topics in Thue Bryndorf's work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (18 papers) and Chromosomal and Genetic Variations (14 papers). Thue Bryndorf is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (18 papers) and Chromosomal and Genetic Variations (14 papers). Thue Bryndorf collaborates with scholars based in Denmark, Germany and Portugal. Thue Bryndorf's co-authors include Tommy Gerdes, Maria Kirchhoff, Claes Lundsteen, Britta Christensen, Brian Christensen, M. Toftager, Anja Pinborg, Lisbeth Prætorius, Anne Zedeler and Kristine Løssl and has published in prestigious journals such as Human Reproduction, Fertility and Sterility and Electrophoresis.

In The Last Decade

Thue Bryndorf

29 papers receiving 976 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thue Bryndorf Denmark	16	516	445	272	251	217	29	997
Gesa Schwanitz Germany	22	1.1k 2.1×	696 1.6×	532 2.0×	140 0.6×	418 1.9×	132	1.6k
Jacques C. Giltay Netherlands	23	760 1.5×	306 0.7×	665 2.4×	249 1.0×	130 0.6×	65	1.3k
Judy Chernos Canada	15	521 1.0×	286 0.6×	375 1.4×	219 0.9×	132 0.6×	38	859
Sandra Chantot‐Bastaraud France	24	939 1.8×	404 0.9×	759 2.8×	304 1.2×	152 0.7×	67	1.4k
J. O. Van Hemel Netherlands	21	809 1.6×	356 0.8×	457 1.7×	94 0.4×	193 0.9×	38	1.1k
Marie‐France Portnoï France	19	574 1.1×	166 0.4×	446 1.6×	111 0.4×	119 0.5×	29	908
Cindy Melotte Belgium	19	813 1.6×	840 1.9×	566 2.1×	118 0.5×	291 1.3×	32	1.5k
Iris Bartels Germany	20	643 1.2×	738 1.7×	305 1.1×	54 0.2×	206 0.9×	69	1.3k
Isabel Lorda‐Sánchez Spain	23	759 1.5×	689 1.5×	558 2.1×	63 0.3×	163 0.8×	67	1.4k
M. Ray Canada	15	731 1.4×	377 0.8×	391 1.4×	61 0.2×	292 1.3×	36	1.1k

Countries citing papers authored by Thue Bryndorf

Since Specialization

Citations

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

Fields of papers citing papers by Thue Bryndorf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thue Bryndorf

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

Friis‐Hansen, Lennart, et al.. (2023). A Novel Approach to Predicting Early Pregnancy Outcomes Dynamically in a Prospective Cohort Using Repeated Ultrasound and Serum Biomarkers. Reproductive Sciences. 30(12). 3597–3609. 1 indexed citations

Toftager, M., Kristine Løssl, Jeanette Bogstad, et al.. (2019). Perinatal outcomes in 521 gestations after fresh and frozen cycles: a secondary outcome of a randomized controlled trial comparing GnRH antagonist versus GnRH agonist protocols. Reproductive BioMedicine Online. 39(4). 659–664. 6 indexed citations

Toftager, M., Randi Sylvest, Lone Schmidt, et al.. (2017). Quality of life and psychosocial and physical well-being among 1,023 women during their first assisted reproductive technology treatment: secondary outcome to a randomized controlled trial comparing gonadotropin-releasing hormone (GnRH) antagonist and GnRH agonist protocols. Fertility and Sterility. 109(1). 154–164. 28 indexed citations

Toftager, M., Kristine Løssl, Lisbeth Prætorius, et al.. (2017). Cumulative live birth rates after one ART cycle including all subsequent frozen–thaw cycles in 1050 women: secondary outcome of an RCT comparing GnRH-antagonist and GnRH-agonist protocols. Human Reproduction. 32(3). 556–567. 102 indexed citations

Toftager, M., Jeanette Bogstad, Thue Bryndorf, et al.. (2016). Risk of severe ovarian hyperstimulation syndrome in GnRH antagonist versus GnRH agonist protocol: RCT including 1050 first IVF/ICSI cycles. Human Reproduction. 31(6). 1253–1264. 115 indexed citations

Stenbæk, Dea Siggaard, M. Toftager, Liv V. Hjordt, et al.. (2014). Mental distress and personality in women undergoing GnRH agonist versus GnRH antagonist protocols for assisted reproductive technology. Human Reproduction. 30(1). 103–110. 12 indexed citations

Bisgaard, Anne‐Marie, et al.. (2007). Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata. Clinical Dysmorphology. 16(2). 109–112. 10 indexed citations

Kirchhoff, Maria, Anne‐Marie Bisgaard, Thue Bryndorf, & Tommy Gerdes. (2006). MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams–Beuren syndrome regions. European Journal of Medical Genetics. 50(1). 33–42. 79 indexed citations

Bisgaard, Anne‐Marie, Maria Kirchhoff, Zeynep Tümer, et al.. (2006). Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features. American Journal of Medical Genetics Part A. 140A(20). 2180–2187. 47 indexed citations

10.

Erdogan, Fikret, Wei Chen, Maria Kirchhoff, et al.. (2006). Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research. 115(3-4). 247–253. 58 indexed citations

11.

Cingöz, Sultan, Anne‐Marie Bisgaard, Iben Bache, et al.. (2006). 4q35 deletion and 10p15 duplication associated with immunodeficiency. American Journal of Medical Genetics Part A. 140A(20). 2231–2235. 9 indexed citations

12.

Gerdes, Tommy, Maria Kirchhoff, & Thue Bryndorf. (2005). Automatic analysis of multiplex ligation‐dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection). Electrophoresis. 26(22). 4327–4332. 19 indexed citations

13.

Bryndorf, Thue, Maria Kirchhoff, B. Andreasson, et al.. (2004). The most common chromosome aberration detected by high-resolution comparative genomic hybridization in vulvar intraepithelial neoplasia is not seen in vulvar squamous cell carcinoma. Cytogenetic and Genome Research. 106(1). 43–48. 12 indexed citations

14.

Schmidt, Peter J., et al.. (2001). Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISH. Clinical Genetics. 59(4). 279–283. 4 indexed citations

15.

Bryndorf, Thue, Claes Lundsteen, Allen N. Lamb, Britta Christensen, & John Philip. (2000). Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples. Acta Obstetricia Et Gynecologica Scandinavica. 79(1). 8–14. 11 indexed citations

16.

Bryndorf, Thue. (1998). Development and clinical studies of in situ hybridization techniques in prenatal diagnosis.. PubMed. 45(3). 298–312. 2 indexed citations

17.

Lundsteen, Claes, Jan Maahr, Britta Christensen, et al.. (1995). Image analysis in comparative genomic hybridization. Cytometry. 19(1). 42–50. 49 indexed citations

18.

Bryndorf, Thue, et al.. (1994). Fluorescence in situ hybridization with a chromosome 21‐specific cosmid contig: 1‐day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells. Prenatal Diagnosis. 14(2). 87–96. 10 indexed citations

19.

Bryndorf, Thue, Britta Christensen, Yang Xiang, Anne‐Marie Lind, & John Philip. (1993). Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells. Prenatal Diagnosis. 13(9). 815–823. 6 indexed citations

20.

Christensen, Britta, et al.. (1992). Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non‐radioactive in situ hybridization. Prenatal Diagnosis. 12(4). 241–250. 28 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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