Hannah Verdin

1.2k total citations
29 papers, 467 citations indexed

About

Hannah Verdin is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hannah Verdin has authored 29 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hannah Verdin's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Sexual Differentiation and Disorders (6 papers) and Prenatal Screening and Diagnostics (6 papers). Hannah Verdin is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Sexual Differentiation and Disorders (6 papers) and Prenatal Screening and Diagnostics (6 papers). Hannah Verdin collaborates with scholars based in Belgium, United States and Netherlands. Hannah Verdin's co-authors include Elfride De Baere, Martine Cools, Françoise Meire, Miriam Bauwens, Frauke Coppieters, Thomy de Ravel, Berenice B. Mendonça, Tom Sante, Björn Menten and Bart P. Leroy and has published in prestigious journals such as Scientific Reports, PLoS Genetics and Human Reproduction.

In The Last Decade

Hannah Verdin

27 papers receiving 463 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hannah Verdin Belgium 14 317 268 69 39 38 29 467
Faouzi Mâazoul Tunisia 13 424 1.3× 345 1.3× 26 0.4× 22 0.6× 23 0.6× 46 567
Ada Rosenmann Israel 16 347 1.1× 252 0.9× 85 1.2× 51 1.3× 17 0.4× 36 650
Deepa Murali United States 7 310 1.0× 104 0.4× 19 0.3× 29 0.7× 12 0.3× 9 381
Sergio A. Cuevas‐Covarrubias Mexico 11 280 0.9× 167 0.6× 60 0.9× 44 1.1× 3 0.1× 41 418
Charles E. Hawkins United States 4 272 0.9× 55 0.2× 60 0.9× 4 0.1× 29 0.8× 4 385
Tom Sante Belgium 12 246 0.8× 209 0.8× 34 0.5× 12 0.3× 1 0.0× 16 473
Glen R. Monroe Netherlands 12 216 0.7× 313 1.2× 3 0.0× 54 1.4× 5 0.1× 20 524
F. Schoute Netherlands 9 455 1.4× 263 1.0× 5 0.1× 98 2.5× 5 0.1× 12 622
Claude‐Lise Richer Canada 15 458 1.4× 397 1.5× 12 0.2× 68 1.7× 4 0.1× 35 759
G.J. te Meerman Netherlands 12 102 0.3× 150 0.6× 26 0.4× 10 0.3× 2 0.1× 15 326

Countries citing papers authored by Hannah Verdin

Since Specialization
Citations

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

Fields of papers citing papers by Hannah Verdin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hannah Verdin

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

All Works

20 of 20 papers shown
1.
Verdin, Hannah, et al.. (2024). Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couples. Journal of Genetic Counseling. 34(1). e1899–e1899. 1 indexed citations
2.
Cools, Martine, Simon J. Tavernier, Petra Schelstraete, et al.. (2023). Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development: a cross-sectional study. European Journal of Endocrinology. 190(1). 34–43. 4 indexed citations
3.
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5.
Potorac, Iulia, Olivier Malaise, Corinne Fasquelle, et al.. (2023). The Role of MCM9 in the Etiology of Sertoli Cell-Only Syndrome and Premature Ovarian Insufficiency. Journal of Clinical Medicine. 12(3). 990–990. 4 indexed citations
6.
Santens, Patrick, et al.. (2022). Marked hypotonia: An additional feature of ANO3-related movement disorder. European Journal of Medical Genetics. 65(12). 104625–104625. 1 indexed citations
7.
Arno, Gavin, Julie De Zaeytijd, Hannah Verdin, et al.. (2020). The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56. Scientific Reports. 10(1). 1289–1289. 21 indexed citations
8.
Verdin, Hannah, et al.. (2020). Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicism. European Journal of Medical Genetics. 63(5). 103918–103918. 6 indexed citations
9.
Verdin, Hannah, et al.. (2019). Update on the genetics of differences of sex development (DSD). Best Practice & Research Clinical Endocrinology & Metabolism. 33(3). 101271–101271. 39 indexed citations
10.
Verdin, Hannah, Ana Fernández‐Miñán, Sara Benito‐Sanz, et al.. (2015). Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape. Scientific Reports. 5(1). 17667–17667. 19 indexed citations
11.
Bauwens, Miriam, Sophie Walraedt, Patricia Delbeke, et al.. (2015). Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus. Investigative Ophthalmology & Visual Science. 56(3). 1701–1710. 23 indexed citations
12.
Coppieters, Frauke, Anne‐Laure Todeschini, Takuro Fujimaki, et al.. (2015). Hidden Genetic Variation in LCA9‐Associated Congenital Blindness Explained by 5′UTR Mutations and Copy‐Number Variations of NMNAT1. Human Mutation. 36(12). 1188–1196. 24 indexed citations
13.
Schil, Kristof Van, Marcus Karlstetter, Françoise Meire, et al.. (2014). Homozygous deletion of glutamate receptor gene GRID2 causes new human hotfoot mutant phenotype, characterized by early-onset cerebellar ataxia and retinal dystrophy. European Journal of Human Genetics. 22. 83–84. 2 indexed citations
14.
Brosens, Erwin, Elisabeth M. de Jong, Tahsin Stefan Barakat, et al.. (2014). Structural and numerical changes of chromosome X in patients with esophageal atresia. European Journal of Human Genetics. 22(9). 1077–1084. 14 indexed citations
15.
Coppieters, Frauke, Kristof Van Schil, Miriam Bauwens, et al.. (2014). Identity-by-descent–guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy. Genetics in Medicine. 16(9). 671–680. 47 indexed citations
16.
Verdin, Hannah, et al.. (2014). Co-occurrence of congenital hydronephrosis and FOXL2-associated blepharophimosis, ptosis, epicanthus inversus syndrome (BPES). European Journal of Medical Genetics. 57(10). 576–578. 6 indexed citations
17.
Schil, Kristof Van, Françoise Meire, Marcus Karlstetter, et al.. (2014). Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion. Genetics in Medicine. 17(4). 291–299. 32 indexed citations
18.
Verdin, Hannah, Barbara D′haene, Diane Beysen, et al.. (2013). Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain. PLoS Genetics. 9(3). e1003358–e1003358. 56 indexed citations
19.
Haghighi, Alireza, et al.. (2012). Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II.. PubMed. 18. 211–8. 14 indexed citations
20.
Verdin, Hannah & Elfride De Baere. (2012). <i>FOXL2 </i>Impairment in Human Disease. Hormone Research in Paediatrics. 77(1). 2–11. 39 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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