Caroline Cazin

1.4k total citations
20 papers, 481 citations indexed

About

Caroline Cazin is a scholar working on Genetics, Reproductive Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Caroline Cazin has authored 20 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 12 papers in Reproductive Medicine and 10 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Caroline Cazin's work include Sperm and Testicular Function (12 papers), Reproductive Biology and Fertility (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Caroline Cazin is often cited by papers focused on Sperm and Testicular Function (12 papers), Reproductive Biology and Fertility (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Caroline Cazin collaborates with scholars based in France, Iran and China. Caroline Cazin's co-authors include Pierre F. Ray, Zine‐Eddine Kherraf, Christophe Arnoult, Charles Coutton, Aminata Touré, Guillaume Martinez, Julie Beurois, Nicolas Thierry‐Mieg, Sélima Fourati Ben Mustapha and Raoudha Zouari and has published in prestigious journals such as Development, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Caroline Cazin

19 papers receiving 476 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Caroline Cazin France	10	312	278	258	190	51	20	481
Yan-Wei Sha China	13	385 1.2×	353 1.3×	283 1.1×	213 1.1×	69 1.4×	29	570
Mariem Ben Khelifa France	7	435 1.4×	347 1.2×	351 1.4×	249 1.3×	68 1.3×	12	626
Sélima Fourati Ben Mustapha France	7	239 0.8×	184 0.7×	191 0.7×	137 0.7×	35 0.7×	13	338
Sandra Yassine France	7	517 1.7×	291 1.0×	473 1.8×	268 1.4×	54 1.1×	7	728
Fuxi Zhu China	13	407 1.3×	300 1.1×	333 1.3×	259 1.4×	70 1.4×	25	593
Thomas Karaouzène France	9	572 1.8×	346 1.2×	519 2.0×	285 1.5×	73 1.4×	10	790
S. Brugo Olmedo Argentina	8	420 1.3×	207 0.7×	296 1.1×	172 0.9×	90 1.8×	15	507
Li Yuan China	10	202 0.6×	162 0.6×	135 0.5×	166 0.9×	19 0.4×	13	358
Sophie Pennetier France	9	124 0.4×	204 0.7×	381 1.5×	340 1.8×	46 0.9×	10	555
Ken Klotz United States	8	335 1.1×	163 0.6×	260 1.0×	157 0.8×	16 0.3×	8	455

Countries citing papers authored by Caroline Cazin

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Cazin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Cazin

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

Amiri‐Yekta, Amir, Florence Hazane‐Puch, Caroline Cazin, et al.. (2024). Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non‐obstructive azoospermia in an Iranian family. Clinical Genetics. 106(5). 625–631. 1 indexed citations

Barbotin, Anne‐Laure, Caroline Cazin, Marie Bidart, et al.. (2024). Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants. Andrology. 13(5). 1137–1148.

Kherraf, Zine‐Eddine, Anne‐Laure Barbotin, Guillaume Martinez, et al.. (2023). A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility. Clinical Genetics. 105(2). 220–225. 4 indexed citations

Sayou, Camille, Patrick Lorès, Caroline Cazin, et al.. (2023). Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans. iScience. 26(8). 107354–107354. 2 indexed citations

Amiri‐Yekta, Amir, Caroline Cazin, Elma El Khouri, et al.. (2023). CCDC65 , encoding a component of the axonemal Nexin‐Dynein regulatory complex, is required for sperm flagellum structure in humans. Clinical Genetics. 105(3). 317–322. 11 indexed citations

Martinez, Guillaume, Anne‐Laure Barbotin, Caroline Cazin, et al.. (2023). New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. International Journal of Molecular Sciences. 24(3). 2559–2559. 9 indexed citations

Loeuillet, Corinne, Caroline Cazin, Zine‐Eddine Kherraf, et al.. (2022). A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females. Clinical Genetics. 102(1). 22–29. 8 indexed citations

Kherraf, Zine‐Eddine, Caroline Cazin, Sélima Fourati Ben Mustapha, et al.. (2022). Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia. The American Journal of Human Genetics. 109(3). 508–517. 74 indexed citations

Cazin, Caroline, Guillaume Martinez, Sélima Fourati Ben Mustapha, et al.. (2021). Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa. International Journal of Molecular Sciences. 22(4). 2187–2187. 6 indexed citations

10.

Lorès, Patrick, Zine‐Eddine Kherraf, Amir Amiri‐Yekta, et al.. (2021). A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome. Human Genetics. 140(7). 1031–1043. 20 indexed citations

11.

Liu, Siyu, Jintao Zhang, Zine‐Eddine Kherraf, et al.. (2021). CFAP61 is required for sperm flagellum formation and male fertility in human and mouse. Development. 148(23). 37 indexed citations

12.

Cazin, Caroline, Yasmine Neirijnck, Corinne Loeuillet, et al.. (2021). Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B. Cells. 11(1). 118–118. 1 indexed citations

13.

Huang, Qian, Wei Li, Qi Zhou, et al.. (2021). Leucine zipper transcription factor-like 1 (LZTFL1), an intraflagellar transporter protein 27 (IFT27) associated protein, is required for normal sperm function and male fertility. Developmental Biology. 477. 164–176. 8 indexed citations

14.

Ray, Pierre F., Fariba Ramezanali, Amir Amiri‐Yekta, et al.. (2021). KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole. European Journal of Obstetrics & Gynecology and Reproductive Biology. 259. 100–104. 2 indexed citations

15.

Beurois, Julie, Caroline Cazin, Zine‐Eddine Kherraf, et al.. (2020). Genetics of teratozoospermia: Back to the head. Best Practice & Research Clinical Endocrinology & Metabolism. 34(6). 101473–101473. 38 indexed citations

16.

Touré, Aminata, Guillaume Martinez, Zine‐Eddine Kherraf, et al.. (2020). The genetic architecture of morphological abnormalities of the sperm tail. Human Genetics. 140(1). 21–42. 144 indexed citations

17.

Arafah, Karim, Fabrice Lopez, Caroline Cazin, et al.. (2020). Defect in the nuclear pore membrane glycoprotein 210-like gene is associated with extreme uncondensed sperm nuclear chromatin and male infertility: a case report. Human Reproduction. 36(3). 693–701. 18 indexed citations

18.

Qü, Wei, Shuo Yuan, Chao Quan, et al.. (2020). The essential role of intraflagellar transport protein IFT81 in male mice spermiogenesis and fertility. American Journal of Physiology-Cell Physiology. 318(6). C1092–C1106. 26 indexed citations

19.

Kherraf, Zine‐Eddine, Caroline Cazin, Charles Coutton, et al.. (2019). Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Clinical Genetics. 96(5). 394–401. 29 indexed citations

20.

Beurois, Julie, Guillaume Martinez, Caroline Cazin, et al.. (2019). CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report. Human Reproduction. 34(10). 2071–2079. 43 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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