Reiner A. Veitia

13.0k total citations · 1 hit paper
187 papers, 8.7k citations indexed

About

Reiner A. Veitia is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Reiner A. Veitia has authored 187 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 140 papers in Molecular Biology, 95 papers in Genetics and 37 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Reiner A. Veitia's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (55 papers), Reproductive Biology and Fertility (35 papers) and Chromosomal and Genetic Variations (32 papers). Reiner A. Veitia is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (55 papers), Reproductive Biology and Fertility (35 papers) and Chromosomal and Genetic Variations (32 papers). Reiner A. Veitia collaborates with scholars based in France, United States and Belgium. Reiner A. Veitia's co-authors include James A. Birchler, Sandrine Caburet, Bérénice A. Benayoun, Marc Fellous, Anne‐Laure Todeschini, Samuel Bottani, Adrien Georges, Julie Cocquet, Elfride De Baere and Frank Batista and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Reiner A. Veitia

183 papers receiving 8.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Gene balance hypothesis: Connecting issues of dosage sensitivity across biological disciplines

2012 397 citations James A. Birchler, Reiner A. Veitia profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Reiner A. Veitia France	54	5.6k	3.8k	2.1k	1.5k	1.3k	187	8.7k
Howard J. Cooke United Kingdom	56	7.8k 1.4×	5.0k 1.3×	3.0k 1.4×	1.1k 0.7×	2.0k 1.6×	161	11.2k
John R. McCarrey United States	51	6.8k 1.2×	4.5k 1.2×	1.1k 0.5×	1.9k 1.2×	2.4k 1.9×	154	9.5k
Wolfgang Engel Germany	53	6.2k 1.1×	3.9k 1.0×	1.2k 0.6×	3.4k 2.2×	3.2k 2.5×	324	11.9k
John C. Schimenti United States	57	7.5k 1.3×	2.6k 0.7×	1.3k 0.6×	1.3k 0.9×	884 0.7×	199	10.0k
Marc Fellous France	54	5.3k 0.9×	5.3k 1.4×	784 0.4×	1.2k 0.8×	2.0k 1.6×	174	9.0k
David C. Page United States	63	9.8k 1.8×	9.7k 2.6×	2.7k 1.3×	2.4k 1.5×	4.3k 3.4×	145	14.8k
Bradley R. Cairns United States	73	16.1k 2.9×	2.4k 0.6×	2.1k 1.0×	1.4k 0.9×	1.5k 1.2×	141	18.4k
Mary Ann Handel United States	45	4.2k 0.7×	2.0k 0.5×	914 0.4×	1.4k 0.9×	1.3k 1.0×	116	5.9k
Norman B. Hecht United States	53	6.1k 1.1×	3.4k 0.9×	634 0.3×	2.4k 1.5×	3.5k 2.7×	185	9.1k
Philippe Berta France	38	6.5k 1.2×	5.8k 1.5×	677 0.3×	454 0.3×	1.7k 1.4×	83	9.4k

Countries citing papers authored by Reiner A. Veitia

Since Specialization

Citations

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

Fields of papers citing papers by Reiner A. Veitia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Reiner A. Veitia. 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 Reiner A. Veitia. The network helps show where Reiner A. Veitia may publish in the future.

Co-authorship network of co-authors of Reiner A. Veitia

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

Grange, Pierre de la, et al.. (2022). Recurrent missense variants in clonal hematopoiesis‐related genes present in the general population. Clinical Genetics. 103(2). 247–251. 2 indexed citations

Llano, Elena, Anne‐Laure Todeschini, Natalia Felipe‐Medina, et al.. (2022). The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell Tumors. Cancer Research. 83(2). 239–250. 14 indexed citations

Veitia, Reiner A. & Hideki Innan. (2021). Pathogenic “germline” variants associated with myeloproliferative disorders in apparently normal individuals: Inherited or acquired genetic alterations?. Clinical Genetics. 101(3). 371–374. 3 indexed citations

Piégu, Benoît, et al.. (2021). Genes Encoding Teleost Orthologs of Human Haploinsufficient and Monoallelically Expressed Genes Remain in Duplicate More Frequently Than the Whole Genome. International Journal of Genomics. 2021. 1–6. 4 indexed citations

Álvarez‐Mora, María Isabel, Anne‐Laure Todeschini, Sandrine Caburet, et al.. (2020). An exome‐wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes. Clinical Genetics. 98(3). 293–298. 13 indexed citations

Veitia, Reiner A.. (2020). Clinical Genetics paving the way to the future. Clinical Genetics. 99(2). 217–218. 1 indexed citations

Felipe‐Medina, Natalia, Sandrine Caburet, Dirk G. de Rooij, et al.. (2020). A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1. eLife. 9. 31 indexed citations

Birchler, James A. & Reiner A. Veitia. (2019). Genomic Balance and Speciation. SHILAP Revista de lepidopterología. 12. 1999482403–1999482403. 5 indexed citations

Johnson, Adam F., Há Thi Nguyen, & Reiner A. Veitia. (2019). Causes and effects of haploinsufficiency. Biological reviews/Biological reviews of the Cambridge Philosophical Society. 94(5). 1774–1785. 49 indexed citations

10.

Fouquet, Baptiste, Patrycja Pawlikowska, Sandrine Caburet, et al.. (2017). A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency. eLife. 6. 51 indexed citations

11.

Georges, Adrien, et al.. (2013). FOXL2: a central transcription factor of the ovary. Journal of Molecular Endocrinology. 52(1). R17–R33. 132 indexed citations

12.

Caburet, Sandrine, Petra Zavadáková, Ziva Ben‐Neriah, et al.. (2012). Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure. LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas).

13.

Benayoun, Bérénice A., Adrien Georges, David L’Hôte, et al.. (2011). Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase. Human Molecular Genetics. 20(9). 1673–1686. 77 indexed citations

14.

Baere, Elfride De, Marc Fellous, & Reiner A. Veitia. (2010). The transcription factor FOXL2 in ovarian function and dysfunction.. Folia Histochemica et Cytobiologica. 47(5). S43–9. 13 indexed citations

15.

L’Hôte, David, Paul Laissue, Catherine Serres, et al.. (2010). Interspecific resources: a major tool for quantitative trait locus cloning and speciation research. BioEssays. 32(2). 132–142. 14 indexed citations

16.

Birchler, James A. & Reiner A. Veitia. (2009). The gene balance hypothesis: implications for gene regulation, quantitative traits and evolution. New Phytologist. 186(1). 54–62. 232 indexed citations

17.

Veitia, Reiner A. & Isaac Salazar‐Ciudad. (2007). Commonalities in fly embryogenesis and mammalian pituitary patterning. Trends in Endocrinology and Metabolism. 18(7). 261–265. 3 indexed citations

18.

Veitia, Reiner A.. (2003). A sigmoidal transcriptional response: cooperativity, synergy and dosage effects. Biological reviews/Biological reviews of the Cambridge Philosophical Society. 78(1). 149–170. 84 indexed citations

19.

Veitia, Reiner A.. (2002). Exploring the etiology of haploinsufficiency. BioEssays. 24(2). 175–184. 241 indexed citations

20.

Ottolenghi, Chris, Iraj Daizadeh, Σοφία Κοσσίδα, et al.. (2000). The genomic structure of C14orf1 is conserved across eukarya. Mammalian Genome. 11(9). 786–788. 5 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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