Anne Goriely

6.1k total citations · 1 hit paper
48 papers, 3.3k citations indexed

About

Anne Goriely is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Anne Goriely has authored 48 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 19 papers in Genetics and 8 papers in Reproductive Medicine. Recurrent topics in Anne Goriely's work include Epigenetics and DNA Methylation (14 papers), Renal and related cancers (12 papers) and Developmental Biology and Gene Regulation (11 papers). Anne Goriely is often cited by papers focused on Epigenetics and DNA Methylation (14 papers), Renal and related cancers (12 papers) and Developmental Biology and Gene Regulation (11 papers). Anne Goriely collaborates with scholars based in United Kingdom, United States and Denmark. Anne Goriely's co-authors include Andrew O.M. Wilkie, Kate G. Storey, Ruth Díez del Corral, Gil McVean, Geoffrey J. Maher, Malcolm Maden, Isabel Olivera-Martínez, Emily Gale, Hana Mlčochová and Jingtao Guo and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Anne Goriely

48 papers receiving 3.3k citations

Hit Papers

align trajectories

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.

The adult human testis transcriptional cell atlas

2018 422 citations Jingtao Guo, Edward J. Grow et al. Cell Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne Goriely United Kingdom	29	2.3k	1.1k	732	569	290	48	3.3k
Ulrich Zechner Germany	36	3.0k 1.3×	1.6k 1.5×	411 0.6×	574 1.0×	420 1.4×	121	4.7k
Yayoi Toyooka Japan	14	3.5k 1.5×	973 0.9×	437 0.6×	838 1.5×	334 1.2×	23	4.1k
Andy Greenfield United Kingdom	31	2.7k 1.2×	1.8k 1.7×	478 0.7×	278 0.5×	244 0.8×	78	3.7k
Enrico Moro Italy	33	2.2k 1.0×	1.4k 1.3×	874 1.2×	188 0.3×	279 1.0×	71	3.3k
Kazuki Kurimoto Japan	28	5.4k 2.4×	1.5k 1.4×	636 0.9×	1.3k 2.3×	349 1.2×	50	6.1k
Françis Poulat France	31	2.6k 1.1×	2.4k 2.2×	1.0k 1.4×	354 0.6×	169 0.6×	74	3.6k
Wilbur R. Harrison United States	25	1.5k 0.7×	1.1k 1.0×	256 0.3×	372 0.7×	194 0.7×	49	2.7k
Ivo J.P. Arnhold Brazil	44	3.5k 1.5×	2.7k 2.5×	1.4k 1.9×	509 0.9×	511 1.8×	186	6.1k
Hidetoshi Hasuwa Japan	23	1.3k 0.6×	386 0.4×	580 0.8×	525 0.9×	118 0.4×	37	3.0k
Giuseppe Pilia United States	23	2.0k 0.9×	1.5k 1.4×	329 0.4×	449 0.8×	233 0.8×	41	2.9k

Countries citing papers authored by Anne Goriely

Since Specialization

Citations

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

Fields of papers citing papers by Anne Goriely

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Goriely

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

Meyts, Ewa Rajpert‐De, Anne Goriely, & Kristian Almstrup. (2024). New analysis of atypical spermatocytic tumours reveals extensive heterogeneity and plasticity of germ cell tumours ^†. The Journal of Pathology. 263(1). 1–4. 1 indexed citations

Bush, Stephen J. & Anne Goriely. (2024). Can the male germline offer insight into mammalian brain size expansion?. Andrology. 1 indexed citations

Goriely, Anne, et al.. (2024). Professionals' views on providing personalized recurrence risks for de novo mutations: Implications for genetic counseling. Journal of Genetic Counseling. 34(1). e1910–e1910. 1 indexed citations

Bush, Stephen J., Seungmin Han, Shinnosuke Suzuki, et al.. (2024). Adult Human, but Not Rodent, Spermatogonial Stem Cells Retain States with a Foetal-like Signature. Cells. 13(9). 742–742. 4 indexed citations

Hallowell, Nina, et al.. (2023). Providing recurrence risk counselling for parents after diagnosis of a serious genetic condition caused by an apparently de novo mutation in their child: a qualitative investigation of the PREGCARE strategy with UK clinical genetics practitioners. Journal of Medical Genetics. 60(9). 925–931. 4 indexed citations

Bush, Stephen J. & Anne Goriely. (2023). Fine-tuning germline mutation rates across evolution. Trends in Genetics. 39(8). 598–599. 1 indexed citations

Guo, Jingtao, Xichen Nie, Hana Mlčochová, et al.. (2020). The Dynamic Transcriptional Cell Atlas of Testis Development during Human Puberty. Cell stem cell. 26(2). 262–276.e4. 190 indexed citations

Guo, Jingtao, Edward J. Grow, Hana Mlčochová, et al.. (2018). The adult human testis transcriptional cell atlas. Cell Research. 28(12). 1141–1157. 422 indexed citations breakdown →

Guo, Jingtao, Edward J. Grow, Chongil Yi, et al.. (2017). Chromatin and Single-Cell RNA-Seq Profiling Reveal Dynamic Signaling and Metabolic Transitions during Human Spermatogonial Stem Cell Development. Cell stem cell. 21(4). 533–546.e6. 195 indexed citations

10.

Giannoulatou, Eleni, Gil McVean, Indira B. Taylor, et al.. (2013). Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline. Proceedings of the National Academy of Sciences. 110(50). 20152–20157. 58 indexed citations

11.

Stavrou, Eleana F. & Anne Goriely. (2012). Santorini mutation detection meeting 2011: Rapid advance in sequencing technology poses challenges for interpretation of genetic variations. Human Mutation. 33(10). 1497–1500. 1 indexed citations

12.

Babbs, Christian, Helen Stewart, Louise Williams, et al.. (2011). Duplication of theEFNB1gene in familial hypertelorism: imbalance in ephrin‐B1 expression and abnormal phenotypes in humans and mice. Human Mutation. 32(8). 930–938. 11 indexed citations

13.

Lim, Jasmine, Anne Goriely, Grete Krag Jacobsen, et al.. (2011). OCT2, SSX and SAGE1 reveal the phenotypic heterogeneity of spermatocytic seminoma reflecting distinct subpopulations of spermatogonia. The Journal of Pathology. 224(4). 473–483. 56 indexed citations

14.

Goriely, Anne, Helen Lord, Jasmine Lim, et al.. (2010). Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: Implications for genetic testing in “paternal age‐effect” syndromes. American Journal of Medical Genetics Part A. 152A(8). 2067–2073. 26 indexed citations

15.

Lower, Karen M., Jim R. Hughes, Marco De Gobbi, et al.. (2009). Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition. Proceedings of the National Academy of Sciences. 106(51). 21771–21776. 74 indexed citations

16.

Twigg, Stephen R.F., Kazuya Matsumoto, Alexa Kidd, et al.. (2006). The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males. The American Journal of Human Genetics. 78(6). 999–1010. 73 indexed citations

17.

Goriely, Anne, et al.. (2005). Fibroblast growth factor receptor 2, gain‐of‐function mutations, and tumourigenesis: investigating a potential link. The Journal of Pathology. 207(1). 27–31. 23 indexed citations

18.

Goriely, Anne, et al.. (2003). Evidence for Selective Advantage of Pathogenic FGFR2 Mutations in the Male Germ Line. Science. 301(5633). 643–646. 213 indexed citations

19.

Goriely, Anne, et al.. (2003). Germ cell selection of an FGFR2 point mutation explains the paternal age effect in Apart syndrome. The American Journal of Human Genetics. 73(5). 565–565. 1 indexed citations

20.

Goriely, Anne, Ruth Díez del Corral, & Kate G. Storey. (1999). c-Irx2 expression reveals an early subdivision of the neural plate in the chick embryo. Mechanisms of Development. 87(1-2). 203–206. 35 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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