Nelly Sabbaghian

3.5k citations

45 papers · 1.9k indexed · h-index 21

Molecular Biology top 10%
Genetics top 5%
Surgery top 5%
Rheumatology top 2%
Pulmonary and Respiratory Medicine top 10%

Co-authors: William D. Foulkes Marc Tischkowitz Isabelle Morin Nancy Hamel Rima Rozen John R. Priest Robert W. Platt Daniel Leclerc
Topics: Congenital Diaphragmatic Hernia Studies (19 papers)BRCA gene mutations in cancer (12 papers)DNA Repair Mechanisms (9 papers)
Cited by: Rheumatology Genetics Cancer Research
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences The Journal of Clinical Endocrinology & Metabolism
Partner nations: Canada United States United Kingdom

In The Last Decade

Nelly Sabbaghian

44 papers receiving 1.8k citations

Peers

Countries citing papers authored by Nelly Sabbaghian

Since Specialization

Citations

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

Fields of papers citing papers by Nelly Sabbaghian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nelly Sabbaghian

This figure shows the co-authorship network connecting the top 25 collaborators of Nelly Sabbaghian. A scholar is included among the top collaborators of Nelly Sabbaghian 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 Nelly Sabbaghian. Nelly Sabbaghian is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Exomic and epigenomic analysis of pulmonary blastoma 2024 ·Lung Cancer ·Najmeh Alirezaie,(unknown),F. Kommoss,Nelly Sabbaghian,(unknown),(unknown),Javad Nadaf,(unknown),Pradeesh Sivapalan,Mark G. Evans,Paul S. Thorner,Pierre Fiset,Andreas von Deimling,William D. Foulkes	1
2	Extraskeletal chondroma of the toe in a child with DICER1 tumor predisposition syndrome: support for a dominant negative mechanism 2024 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·(unknown),Nelly Sabbaghian,(unknown),John R. Priest,(unknown),(unknown),Marc R. Fabian,William D. Foulkes	0
3	DICER1 platform domain missense variants inhibit miRNA biogenesis and lead to tumor susceptibility 2023 ·NAR Cancer ·(unknown),(unknown),Mona K. Wu,(unknown),(unknown),Nelly Sabbaghian,Marc R. Fabian,William D. Foulkes	2
4	An Unusual Enteric Yolk Sac Tumor: First Report of an Ovarian Germ Cell Tumor Associated With a Germline Pathogenic Variant in DICER1 2021 ·International Journal of Gynecological Pathology ·W. Glenn McCluggage,Lili Fu,(unknown),Leanne de Kock,Nelly Sabbaghian,(unknown),Colin J.R. Stewart,C. Blake Gilks,William D. Foulkes	2
5	Intrathyroidal Thymus (Incidentaloma) Mimicking Thyroid Neoplasia in DICER1 Syndrome 2020 ·European Thyroid Journal ·Marek Niedziela,Nelly Sabbaghian,Leanne de Kock,William D. Foulkes	1
6	Analysis of DICER1 in familial and sporadic cases of transposition of the great arteries 2018 ·Congenital Heart Disease ·Nelly Sabbaghian,M. Cristina Digilio,Gillian M. Blue,Timothée Revil,David S. Winlaw,William D. Foulkes	2
7	Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada 2014 ·Hereditary Cancer in Clinical Practice ·Taila Hartley,Luca Cavallone,Nelly Sabbaghian,Rachel Silva‐Smith,Nancy Hamel,Olga Aleynikova,(unknown),(unknown),Pedro Pinto,Marc Tischkowitz,Eva Tomiak,William D. Foulkes	18
8	Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2 2013 ·BMC Medical Genomics ·Tú Nguyen‐Dumont,Zhi L. Teo,Bernard J. Pope,Fleur Hammet,Maryam Mahmoodi,Helen Tsimiklis,Nelly Sabbaghian,Marc Tischkowitz,William D. Foulkes,Graham G. Giles,John L. Hopper,(unknown),Melissa C. Southey,(unknown)	12
9	Contribution of the PALB2 c.2323C>T [p.Q775X] Founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent 2013 ·BMC Medical Genetics ·(unknown),Nelly Sabbaghian,Nancy Hamel,(unknown),William D. Foulkes,Anne‐Marie Mes‐Masson,Diane Provencher,Patricia N. Tonin	17
10	Heterozygous mutations in the PALB2 hereditary breast cancer predisposition gene impact on the three‐dimensional nuclear organization of patient‐derived cell lines 2013 ·Genes Chromosomes and Cancer ·Landon Wark,David J. Novak,Nelly Sabbaghian,Lilian Amrein,Jaganmohan R. Jangamreddy,Mary Cheang,(unknown),Raquel Aloyz,William D. Foulkes,Sabine Mai,Marc Tischkowitz	5
11	Rare germline mutations inPALB2and breast cancer risk: A population-based study 2012 ·Human Mutation ·Marc Tischkowitz,Marinela Capanu,Nelly Sabbaghian,Lili Li,Xiaolin Liang,Maxime Vallée,Sean V. Tavtigian,Patrick Concannon,William D. Foulkes,Leslie Bernstein,(unknown),Jonine L. Bernstein,Colin B. Begg	59
12	Germline PALB2 mutation analysis in breast–pancreas cancer families: Table 1 2011 ·Journal of Medical Genetics ·Zsofia K. Stadler,Erin Salo‐Mullen,Nelly Sabbaghian,James A. Simon,Li Zhang,Sara H. Olson,Robert C. Kurtz,Kenneth Offit,William D. Foulkes,Mark E. Robson,Marc Tischkowitz	22
13	Extending the phenotypes associated withDICER1mutations 2011 ·Human Mutation ·William D. Foulkes,(unknown),Nancy Hamel,Barbara Pasini,Sofia Asioli,Gareth Baynam,Catherine S. Choong,Adrian Charles,(unknown),Megan K. Dishop,Nicole Graf,Mesiha Ekim,Dorothée Bouron‐Dal Soglio,Jocelyne Arseneau,Robert H. Young,Nelly Sabbaghian,Archana Srivastava,Marc Tischkowitz,John R. Priest	143
14	A PALB2 mutation associated with high risk of breast cancer 2010 ·Breast Cancer Research ·Melissa C. Southey,Zhi L. Teo,James G. Dowty,Fabrice Odefrey,Daniel J. Park,Marc Tischkowitz,Nelly Sabbaghian,Carmel Apicella,Graham Byrnes,Ingrid Winship,Laura Baglietto,Graham G. Giles,David E. Goldgar,William D. Foulkes,John L. Hopper,(unknown),(unknown)	89
15	Analysis of the gene coding for the BRCA2‐Interacting protein PALB2 in hereditary prostate cancer 2008 ·The Prostate ·Marc Tischkowitz,Nelly Sabbaghian,Anna M. Ray,Ethan M. Lange,William D. Foulkes,Kathleen A. Cooney	28
16	Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases 2008 ·Breast Cancer Research and Treatment ·David J. Novak,Nelly Sabbaghian,Philippe Maillet,Pierre O. Chappuis,William D. Foulkes,Marc Tischkowitz	17
17	Identification of a novel truncating PALB2mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women 2007 ·Breast Cancer Research ·William D. Foulkes,Parviz Ghadirian,(unknown),Nancy Hamel,Sylvie Giroux,Nelly Sabbaghian,Andrew D. Darnel,Robert E. Royer,Aletta Poll,(unknown),André Robidoux,G. Martin,Tarek A. Bismar,Marc Tischkowitz,François Rousseau,Steven A. Narod	107
18	Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk 2003 ·Molecular Genetics and Metabolism ·Isabelle Morin,Angela M. Devlin,Daniel Leclerc,Nelly Sabbaghian,Charles H. Halsted,Richard H. Finnell,Rima Rozen	62
19	Antisense inhibition of methylenetetrahydrofolate reductase reduces survival of methionine-dependent tumour lines 2002 ·British Journal of Cancer ·Jasjeet S. Sekhon,Patrı́cia Pereira,Nelly Sabbaghian,Andrea R. Schievella,Rima Rozen	11
20	Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects 1999 ·American Journal of Medical Genetics ·Benedicte Christensen,Laura Arbour,Pamela V. Tran,Daniel Leclerc,Nelly Sabbaghian,Robert W. Platt,Brian M. Gilfix,David S. Rosenblatt,Roy A. Gravel,Patricia Forbes,Rima Rozen	237

About Nelly Sabbaghian

Nelly Sabbaghian is a scholar working on Surgery, Genetics and Cancer Research, having authored 45 papers that have together received 1.9k indexed citations. Recurring topics across this work include Congenital Diaphragmatic Hernia Studies (19 papers), BRCA gene mutations in cancer (12 papers) and DNA Repair Mechanisms (9 papers). The work is most often cited by research in Rheumatology (425 citations), Genetics (631 citations) and Cancer Research (268 citations). Nelly Sabbaghian has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include William D. Foulkes, Marc Tischkowitz, Isabelle Morin, Nancy Hamel, Rima Rozen, John R. Priest, Robert W. Platt, Daniel Leclerc, Leanne de Kock and Victor Cohen. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Journal of Clinical Endocrinology & Metabolism.

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.

Explore authors with similar magnitude of impact