Carine Bonnard

3.7k total citations
40 papers, 1.2k citations indexed

About

Carine Bonnard is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Carine Bonnard has authored 40 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Genetics and 5 papers in Epidemiology. Recurrent topics in Carine Bonnard's work include BRCA gene mutations in cancer (6 papers), Estrogen and related hormone effects (5 papers) and Neurological diseases and metabolism (4 papers). Carine Bonnard is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Estrogen and related hormone effects (5 papers) and Neurological diseases and metabolism (4 papers). Carine Bonnard collaborates with scholars based in Singapore, United Kingdom and United States. Carine Bonnard's co-authors include Martin L. Hibberd, Jianjun Liu, Sonia Dávila, Mark Seielstad, Yi Li, Bruno Reversade, Anbupalam Thalamuthu, Eng‐King Tan, Lisa Skipper and Pavanni Ratnagopal and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and The Journal of Experimental Medicine.

In The Last Decade

Carine Bonnard

39 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carine Bonnard Singapore 18 461 208 204 188 171 40 1.2k
Moustafa Attar United Kingdom 14 572 1.2× 263 1.3× 419 2.1× 187 1.0× 126 0.7× 26 1.3k
Fabrice Chareyre France 17 546 1.2× 251 1.2× 308 1.5× 313 1.7× 307 1.8× 21 1.4k
Péter Kósa United States 26 832 1.8× 183 0.9× 236 1.2× 242 1.3× 188 1.1× 58 1.9k
Shuaiyao Lu China 18 788 1.7× 211 1.0× 96 0.5× 89 0.5× 141 0.8× 60 1.6k
Nicole L. Rosin Canada 19 467 1.0× 68 0.3× 270 1.3× 132 0.7× 50 0.3× 34 1.4k
Kevin D. Pavelko United States 23 437 0.9× 136 0.7× 770 3.8× 358 1.9× 124 0.7× 71 2.0k
Masahiro Morimoto Japan 18 261 0.6× 95 0.5× 229 1.1× 117 0.6× 68 0.4× 85 955
Julie H. Huang United States 12 631 1.4× 87 0.4× 530 2.6× 71 0.4× 209 1.2× 15 1.8k
Hjalmar Kurzen Germany 25 629 1.4× 95 0.5× 174 0.9× 415 2.2× 60 0.4× 59 2.3k
Fredrik Eriksson Sweden 17 290 0.6× 106 0.5× 307 1.5× 65 0.3× 157 0.9× 21 976

Countries citing papers authored by Carine Bonnard

Since Specialization
Citations

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

Fields of papers citing papers by Carine Bonnard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carine Bonnard

This figure shows the co-authorship network connecting the top 25 collaborators of Carine Bonnard. A scholar is included among the top collaborators of Carine Bonnard 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 Carine Bonnard. Carine Bonnard 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.
Chin, Jiah Shin, Priscilla Lay Keng Lim, Bhavya Sharma, et al.. (2025). Secretome from prolonged high‐density human Wharton's jelly stem cell culture accelerates wound healing in both in vitro and in vivo models. International Wound Journal. 22(5). e70033–e70033. 1 indexed citations
2.
Tham, Khek‐Chian, Sze Han Lee, Helen Williams, et al.. (2025). A role for arginase in skin epithelial differentiation and antimicrobial peptide production. British Journal of Dermatology. 193(1). 125–135. 1 indexed citations
3.
Lim, Priscilla Lay Keng, Khek‐Chian Tham, Yi Zhen Ng, et al.. (2023). Automated Electrical Stimulation Therapy Accelerates Re-Epithelialization in a Three-Dimensional In Vitro Human Skin Wound Model. Advances in Wound Care. 13(5). 217–234. 1 indexed citations
4.
Robinson, Kim S., Gee Ann Toh, Khek‐Chian Tham, et al.. (2023). Diphtheria toxin activates ribotoxic stress and NLRP1 inflammasome-driven pyroptosis. The Journal of Experimental Medicine. 220(10). 29 indexed citations
5.
Paul, Franziska, Fathiya Al-Murshedi, Breana Cham, et al.. (2023). Inactivation of DRG1, encoding a translation factor GTPase, causes a recessive neurodevelopmental disorder. Genetics in Medicine. 25(9). 100893–100893. 1 indexed citations
6.
Tan, Shi Hua, et al.. (2022). Design of hydrogel-based scaffolds for in vitro three-dimensional human skin model reconstruction. Acta Biomaterialia. 153. 13–37. 44 indexed citations
7.
Bonnard, Carine, Naveenan Navaratnam, Thong Teck Tan, et al.. (2020). A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling. The Journal of Experimental Medicine. 217(12). 35 indexed citations
8.
Chia, Poh Hui, Franklin L. Zhong, Shinsuke Niwa, et al.. (2018). A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability. eLife. 7. 44 indexed citations
9.
Shboul, Mohammad, Paul Roschger, Rudolf Ganger, et al.. (2018). Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease. Bone. 123. 48–55. 7 indexed citations
10.
Shboul, Mohammad, Valério Taverniti, Carine Bonnard, et al.. (2015). Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects. Human Molecular Genetics. 24(11). 3163–3171. 25 indexed citations
11.
Dávila, Sonia, Fieke E. M. Froeling, Carine Bonnard, et al.. (2010). New genetic associations detected in a host response study to hepatitis B vaccine. Genes and Immunity. 11(3). 232–238. 65 indexed citations
12.
Low, Yen Ling, Yuqing Li, Keith Humphreys, et al.. (2010). Multi-Variant Pathway Association Analysis Reveals the Importance of Genetic Determinants of Estrogen Metabolism in Breast and Endometrial Cancer Susceptibility. PLoS Genetics. 6(7). e1001012–e1001012. 35 indexed citations
13.
Einarsdóttir, Kristjana, Hatef Darabi, Kamila Czene, et al.. (2009). Common genetic variability in ESR1 and EGF in relation to endometrial cancer risk and survival. British Journal of Cancer. 100(8). 1358–1364. 11 indexed citations
14.
Dávila, Sonia, Martin L. Hibberd, Edhyana Sahiratmadja, et al.. (2008). Genetic Association and Expression Studies Indicate a Role of Toll-Like Receptor 8 in Pulmonary Tuberculosis. PLoS Genetics. 4(10). e1000218–e1000218. 205 indexed citations
15.
Einarsdóttir, Kristjana, Hatef Darabi, Yi Li, et al.. (2008). ESR1 and EGFgenetic variation in relation to breast cancer risk and survival. Breast Cancer Research. 10(1). R15–R15. 28 indexed citations
16.
Einarsdóttir, Kristjana, Lena Rosenberg, Keith Humphreys, et al.. (2006). Comprehensive analysis of the ATM, CHEK2 and ERBB2genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study. Breast Cancer Research. 8(6). R67–R67. 16 indexed citations
17.
Einarsdóttir, Kristjana, Keith Humphreys, Carine Bonnard, et al.. (2006). Effect of ATM, CHEK2 and ERBB2 TAGSNPs and haplotypes on endometrial cancer risk. Human Molecular Genetics. 16(2). 154–164. 18 indexed citations
18.
Einarsdóttir, Kristjana, Keith Humphreys, Carine Bonnard, et al.. (2006). Linkage Disequilibrium Mapping of CHEK2: Common Variation and Breast Cancer Risk. PLoS Medicine. 3(6). e168–e168. 33 indexed citations
19.
Skipper, Lisa, Yi Li, Carine Bonnard, et al.. (2005). Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease. Human Molecular Genetics. 14(23). 3549–3556. 62 indexed citations
20.
Junier, Thomas, et al.. (1999). The Eukaryotic Promoter Database (EPD): recent developments. Nucleic Acids Research. 27(1). 307–309. 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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