Olga M. Sinilnikova

9.5k citations

39 papers · 1.4k indexed · h-index 21

Aging top 5%
Genetics top 2%
- BRCA gene mutations in cancer 25
- Genomic variations and chromosomal abnormalities 14
- Nutrition, Genetics, and Disease 6
Cancer Research top 5%
- Cancer Genomics and Diagnostics 6
Molecular Biology top 10%
- DNA Repair Mechanisms 9
- CRISPR and Genetic Engineering 5
- RNA and protein synthesis mechanisms 5
- RNA Research and Splicing 5
Pathology and Forensic Medicine top 10%

Co-authors: Sylvie Mazoyer Gilbert Lenoir Dominique Stoppa‐Lyonnet Nadine Puget Henry T. Lynch Dominique Stoppa-Lyonnet Sabine Pagès Monique Buisson
Cited by: Aging Genetics Cancer Research
Partner nations: France United States Australia

In The Last Decade

Olga M. Sinilnikova

39 papers receiving 1.4k citations

Peers

Countries citing papers authored by Olga M. Sinilnikova

Since Specialization

Citations

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

Fields of papers citing papers by Olga M. Sinilnikova

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Olga M. Sinilnikova. 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 Olga M. Sinilnikova. The network helps show where Olga M. Sinilnikova may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Olga M. Sinilnikova, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Olga M. Sinilnikova Line = papers co-authored together Olga M. Sinilnikova links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2 Sophie Blein,Laure Barjhoux,(unknown),Francesca Damiola,Marie‐Gabrielle Dondon,Séverine Eon‐Marchais,Morgane Marcou,Olivier Caron,Alain Lortholary,Bruno Buecher,Philippe Vennin,Pascaline Berthet,Catherine Noguès,Christine Lasset,Marion Gauthier‐Villars,Sylvie Mazoyer,Dominique Stoppa‐Lyonnet,Nadine Andrieu,Gilles Thomas,Olga M. Sinilnikova,David G. Cox	2015	9
2	BRCA2 Deep Intronic Mutation Causing Activation of a Cryptic Exon: Opening toward a New Preventive Therapeutic Strategy Olga Anczuków,Monique Buisson,Mélanie Léoné,Christine Coutanson,Christine Lasset,Alain Calender,Olga M. Sinilnikova,Sylvie Mazoyer	2012	52
3	FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer Daniel J. Park,Fabrice Odefrey,Fleur Hammet,Graham G. Giles,Laura Baglietto,ABCFS,MCCS,John L. Hopper,Daniel F. Schmidt,Enes Makalic,Olga M. Sinilnikova,David E. Goldgar,Melissa C. Southey	2011	12
4	The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers Amandine I. Garcia,David G. Cox,Laure Barjhoux,Carole Verny-Pierre,Daniel R. Barnes,(unknown),Antonis C. Antoniou,Dominique Stoppa‐Lyonnet,Olga M. Sinilnikova,Sylvie Mazoyer	2011	39
5	Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2 Tú Nguyen‐Dumont,Lars Petter Jordheim,Jocelyne Michelon,Nathalie Forey,Sandrine McKay‐Chopin,Olga M. Sinilnikova,Florence Le Calvez‐Kelm,Melissa C. Southey,Sean V. Tavtigian,Fabienne Lesueur	2011	6
6	Oncogénétique: estimation des besoins de la population en France pour les dix ans à venir C. Bonaïti-Pellié,N. Andrieu,Patrick Arveux,Valérie Bonadona,Bruno Buecher,Marc Delpech,Damien Jolly,Claire Julian‐Reynier,E. Luporsi,Catherine Noguès,F. Nowak,Sylviane Olschwang,Fernanda Andrade Orsi,Pascal Pujol,Jean‐Christophe Saurin,Olga M. Sinilnikova,D. Stoppa-Lyonnet,F. Thépot	2009	13
7	Analysis of 17β-hydroxysteroid dehydrogenase types 5, 7, and 12 genetic sequence variants in breast cancer cases from French Canadian Families with high risk of breast and ovarian cancer Marie Plourde,Alexandra Ferland,Penny Soucy,Yosr Hamdi,Martine Tranchant,Francine Durocher,Olga M. Sinilnikova,Van Luu The,Jacques Simard	2009	11
8	Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes Marc S. Greenblatt,Lawrence C. Brody,William D. Foulkes,Maurizio Genuardi,Robert M.W. Hofstra,Magali Olivier,Sharon E. Plon,Rolf H. Sijmons,Olga M. Sinilnikova,Amanda B. Spurdle,(unknown)	2008	30
9	Prediction and assessment of splicing alterations: implications for clinical testing Amanda B. Spurdle,Fergus J. Couch,Frans B.L. Hogervorst,Paolo Radice,Olga M. Sinilnikova,(unknown)	2008	86
10	BRCA1 and BRCA2 Mutations in Breast and Ovarian Cancer Syndrome: Reflection on the Creighton University Historical Series of High Risk Families Olga M. Sinilnikova,Sylvie Mazoyer,Colette Bonnardel,Henry T. Lynch,Steven A. Narod,Gilbert Lenoir	2006	17
11	Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers Georgia Chenevix‐Trench,Olga M. Sinilnikova,Graeme Suthers,Nirmala Pandeya,Sylvie Mazoyer,Joseph Sambrook,Sandra Goldup,David E. Goldgar,Henry T. Lynch,Gilbert Lenoir,Glenice Cheetham,kConFab	2005	2
12	Analysis of breast cancer risk modifying candidate genes in BRCA1 and BRCA2 mutation carriers David J. Hughes,Isabelle Coupier,Laure Barjhoux,Sophie M. Ginolhac,David E. Goldgar,Dominique Stoppa‐Lyonnet,Olga M. Sinilnikova	2004	2
13	Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: A population‐based study Sílvia de Sanjosé,Mélanie Léoné,V. Berez,Á. Izquierdo,Rebeca Font,Joan Brunet,Thierry Louat,L. Vilardell,Joan Borràs,P. Viladiu,F. Xavier Bosch,Gilbert Lenoir,Olga M. Sinilnikova	2003	90
14	Cancer Patients Who Experienced Diagnostic Genetic Testing for Cancer Susceptibility Valérie Bonadona,P. Saltel,Françoise Desseigne,H. Mignotte,Jean‐Christophe Saurin,Qīng Wáng,Olga M. Sinilnikova,Sophie Giraud,Gilles Freyer,Henri Plauchu,Alain Puisieux,Christine Lasset	2002	1
15	Distinct BRCA1 Rearrangements Involving the BRCA1 Pseudogene Suggest the Existence of a Recombination Hot Spot Nadine Puget,Sophie Gad,Laure Perrin-Vidoz,Olga M. Sinilnikova,Dominique Stoppa‐Lyonnet,Gilbert Lenoir,Sylvie Mazoyer	2002	88
16	BRCA1 andBRCA2 sequence variants in Chinese breast cancer families Xiangcheng Zhi,Csilla I. Szabo,Sandrine Chopin,Nicola M. Suter,Qing-Sheng Wang,Elaine A. Ostrander,Olga M. Sinilnikova,Gilbert Lenoir,David E. Goldgar,Yu-Rong Shi	2002	34
17	BRCA1 and BRCA2 in Indian breast cancer patients Sunita Saxena,Csilla I. Szabo,Sandrine Chopin,Laure Barjhoux,Olga M. Sinilnikova,Gilbert Lenoir,David E. Goldgar,Dinesh Bhatanager	2002	55
18	BRCA1andBRCA2mutation analysis of early-onset and familial breast cancer cases in Mexico Pablo Ruíz-Flores,Olga M. Sinilnikova,Michael D. Badzioch,Ana Laura Calderón‐Garcidueñas,Sandrine Chopin,Fabrice Odefrey,Juan Francisco González-Guerrero,Csilla I. Szabo,Gilbert Lenoir,David E. Goldgar,Hugo A. Barrera‐Saldaña	2002	49
19	Regulation of dauer larva development in Caenorhabditis elegans by daf-18, a homologue of the tumour suppressor PTEN Jean-Pierre Rouault,Patricia E. Kuwabara,Olga M. Sinilnikova,Laurent Duret,Danielle Thierry‐Mieg,Marc Billaud	1999	124
20	Marker segregation information in breast/ovarian cancer genetic counseling: Is it still useful? Laurent Essioux,C. Girodet,Olga M. Sinilnikova,Sabine Pag�s,François Eisinger,Sandrina de R�sende,Christine Maugard,Didier Lano�,Michel Longy,Yves‐Jean Bignon,Hagay Sobol,Catherine Bona�ti-Pelli�,Dominique Stoppa‐Lyonnet	1998	4

About Olga M. Sinilnikova

Olga M. Sinilnikova is a scholar working on Genetics, Cancer Research and Aging, having authored 39 papers that have together received 1.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (25 papers), Genomic variations and chromosomal abnormalities (14 papers), DNA Repair Mechanisms (9 papers), Nutrition, Genetics, and Disease (6 papers), Cancer Genomics and Diagnostics (6 papers), CRISPR and Genetic Engineering (5 papers), RNA and protein synthesis mechanisms (5 papers) and RNA Research and Splicing (5 papers). The work is most often cited by research in Aging (72 citations), Genetics (791 citations) and Cancer Research (341 citations). Olga M. Sinilnikova has collaborated with scholars based in France, United States and Australia. Frequent co-authors include Sylvie Mazoyer, Gilbert Lenoir, Dominique Stoppa‐Lyonnet, Nadine Puget, Henry T. Lynch, Dominique Stoppa-Lyonnet, Sabine Pagès, Monique Buisson, Jean-Pierre Rouault and Marc Billaud.

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