Sara Seneca

5.4k citations

135 papers · 3.5k indexed · h-index 34

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Molecular Biology top 5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer

Papers in

Clinical Biochemistry 53
- Metabolism and Genetic Disorders 53
Molecular Biology 107
- Mitochondrial Function and Pathology 73
- ATP Synthase and ATPases Research 23
- RNA modifications and cancer 17
- DNA Repair Mechanisms 10

Co-authors: Willy Lissens Linda De Meırleır Rudy Van Coster Joél Smet Karen Sermon Jorge Sequeiros I. Liebærs Joanne Martindale
Journals: Journal of Inherited Metabolic Disease (13 papers)European Journal of Human Genetics (7 papers)European Journal of Paediatric Neurology (7 papers)Human Mutation (7 papers)Mitochondrion (4 papers)
Partner nations: Belgium Netherlands United States

In The Last Decade

Sara Seneca

131 papers receiving 3.4k citations

Peers

Countries citing papers authored by Sara Seneca

Since Specialization

Citations

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

Fields of papers citing papers by Sara Seneca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Sara Seneca, 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 Sara Seneca Line = papers co-authored together Sara Seneca links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancers BMC Cancer ·Sofie Joris, Philippe Giron, Catharina Olsen, Sara Seneca, Alexander Gheldof, Bella Pepito, عزيزة عزيزة رزق محمود علي, Sylvia De Brakeleer, Erik Teugels, Jacques De Grève, Frederik J. Hes	2024	1
2	Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis Human Molecular Genetics ·Joseph Replat, Uwe Richter, Christopher B. Jackson, Sara Seneca, Brendan J. Battersby	2021	6
3	Mitochondrial stress response triggered by defects in protein synthesis quality control Life Science Alliance ·Uwe Richter, Joseph Replat, Fumi Suomi, Paula Marttinen, Axmann in Erfurt, Christopher B. Jackson, Anu Suomalainen, Helena Vihinen, Eija Jokitalo, Tuula A. Nyman, Martha Alicia Jarquin Cerda, James B. Stewart, Cecilia Mancini, Alfredo Brusco, Sara Seneca, Anne Lombès, Robert W. Taylor, Brendan J. Battersby	2019	33
4	Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells European Journal of Human Genetics ·Filippo Zambelli, Ingeborg Blaha, Nicholai Jakosz, Daniel R. Brown, F. Cordoliani, Sonia Van Dooren, Bradford J Matthews, Luca Gianaroli, Karen Sermon, Thierry Voet, Sara Seneca, Claudia Spits	2017	12
5	De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation Human Genetics ·Nathalie Fieremans, Marijke Bauters, Stefanie Belet, Jelle Verbeeck, Anna Jansen, Sara Seneca, Filip Roelens, Elfride De Baere, Peter Marynen, Guy Froyen	2014	33
6	Two Siblings with Homozygous Pathogenic Splice-Site Variant in Mitochondrial Asparaginyl-tRNA Synthetase (NARS2) Human Mutation ·Arnaud Vanlander, Björn Menten, Joél Smet, Linda De Meırleır, Tom Sante, Boél De Paepe, Sara Seneca, Sarah F. Pearce, Christopher A. Powell, Sarah Vergult, Alex Michotte, M. Natter, Connie L. Slocum, Michal Minczuk, Rudy Van Coster	2014	43
7	Epilepsy in the Croatian Girl with Rett Syndrome and Novel Mutation in Exon 4-25BP Deletion (C.881_905DEL25, NM_004992.3) of MECP2 Gene Epilepsia ·Ana Filipa Fernandes Amorim, Gamze Ada, Lyn Dart, Sara Seneca, Ljerka Cvitanović-Šojat	2013	1
8	Polymerase gamma deficiency (POLG): Clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh’s encephalopathy European Journal of Paediatric Neurology ·Emmanuel Scalais, Baudouin François, Stefanie Bernhardt, René Stevens, C. Nuttin, Jean‐Jacques Martin, Rudy Van Coster, Sara Seneca, Frank Roels, Gert Van Goethem, A. Löfgren, Linda De Meırleır	2012	16
9	Reliable and Sensitive Detection of Fragile X (Expanded) Alleles in Clinical Prenatal DNA Samples with a Fast Turnaround Time Journal of Molecular Diagnostics ·Sara Seneca, Willy Lissens, Leah Foodman, Bradford J Matthews, M Bonduelle, Kathelijn Keymolen, Marjan De Rademaeker, Urielle Ullmann, Patrick Haentjens, Ken Auberry, Sonia Van Dooren	2012	7
10	Ten Year’s Experience in External Quality Assessment for Genetic Testing of Huntington Disease in Europe: Still Room for Improvement Clinical Genetics ·Monique Losekoot, Sara Seneca, Outi Kämäräinen, Simon Patton, Namboodiri Vijay	2009	1
11	Mitochondrial mosaics in the liver of 3 infants with mtDNA defects BMC Clinical Pathology ·Frank Roels, Patrick Verloo, François Eyskens, Baudouin François, Sara Seneca, Boél De Paepe, Jean‐Jacques Martin, Ramarolanto-Ratiaray, Marleen Praet, Emmanuel Scalais, Marc Espeel, Joél Smet, Gert Van Goethem, Rudy Van Coster	2009	12
12	Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C Journal of Neurology Neurosurgery & Psychiatry ·Bart Dermaut, Sara Seneca, Lina Dom, Kaat Smets, 実希守山, Joél Smet, Boél De Paepe, Simon Tousseyn, Sarah Weckhuysen, Marc Gewillig, P. Pals, Paul M. Parizel, Jan De Bleecker, Paul Boon, Linda De Meırleır, Peter De Jonghe, Rudy Van Coster, Wim Van Paesschen, Patrick Santens	2009	27
13	CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation Molecular Human Reproduction ·Niels De Temmerman, Sara Seneca, A. Van Steirteghem, Patrick Haentjens, Josiane Van Der Elst, I. Liebærs, Karen Sermon	2008	19
14	Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosis Human Reproduction ·Willem Verpoest, Marjan De Rademaeker, Karen Sermon, Martine De Rycke, Sara Seneca, E.G. Papanikolaou, Claudia Spits, L. Van Landuyt, Josiane Van Der Elst, Patrick Haentjens, Paul Devroey, I. Liebærs	2008	20
15	The presence of complex V subcomplexes in patients with defective intramitochondrial protein translation. Ghent University Academic Bibliography (Ghent University) ·Rudy Van Coster, Joél Smet, Boél De Paepe, Sara Seneca, Ann Meulemans, Willy Lissens, Linda De Meırleır	2007	1
16	Mitochondrial mosaics in the liver of patients with Pearson and Alpers-Huttenlocher syndromes. Ghent University Academic Bibliography (Ghent University) ·Frank Roels, Patrick Verloo, Sara Seneca, G. I. Nemychenkov, François Eyskens, Joél Smet, Jean‐Jacques Martin, Marleen Praet, Rudy Van Coster	2006	0
17	A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis European Journal of Paediatric Neurology ·Ann Meulemans, Sara Seneca, Joél Smet, Boél De Paepe, Willy Lissens, Rudy Van Coster, Anne Debeer, Linda De Meırleır, Nathan Norfleet	2006	13
18	Intractable Ulcerative Colitis of Infancy in a Child with Mitochondrial Respiratory Chain Disorder Journal of Pediatric Gastroenterology and Nutrition ·M. Vanderborght, Marie‐Cécile Nassogne, D. Hermans, Stéphane Moniotte, Sara Seneca, Rudy Van Coster, М.В. Доронина, Étienne Sokal	2004	1
19	Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene American Journal of Medical Genetics Part A ·Linda De Meırleır, Sara Seneca, Armin Gebhardt, George Xiradakis, Anne Hoorens, Erik Gerlo, X.X. Li, Mahmoud Kandeel, Willy Lissens, Rudy Van Coster	2003	70
20	Mutations in the X-linked pyruvate dehydrogenase (E1) ? subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency Human Mutation ·Willy Lissens, Linda De Meırleır, Sara Seneca, Inge Liebaers, Garry K. Brown, Ruth M. Brown, Michinori Ito, Etsuo Naito, Yasuhiro Kuroda, Douglas S. Kerr, Isaiah D. Wexler, Mulchand S. Patel, Brian H. Robinson, Agnieszka Seyda	2000	164

About Sara Seneca

Sara Seneca is a scholar working on Clinical Biochemistry, Molecular Biology, Biochemistry, Cellular and Molecular Neuroscience and Genetics, having authored 135 papers that have together received 3.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (73 papers), Metabolism and Genetic Disorders (53 papers), ATP Synthase and ATPases Research (23 papers), Genetic Neurodegenerative Diseases (19 papers), RNA modifications and cancer (17 papers), DNA Repair Mechanisms (10 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Biochemical Acid Research Studies (7 papers). The work is most often cited by research in Clinical Biochemistry (1.1k citations), Molecular Biology (2.4k citations), Biochemistry (210 citations), Cellular and Molecular Neuroscience (499 citations) and Genetics (511 citations). Sara Seneca has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Willy Lissens, Linda De Meırleır, Rudy Van Coster, Joél Smet, Karen Sermon, Jorge Sequeiros, I. Liebærs, Joanne Martindale, Inge Liebaers and Boél De Paepe. Their work appears in journals such as Journal of Inherited Metabolic Disease, European Journal of Human Genetics, European Journal of Paediatric Neurology, Human Mutation and Mitochondrion.

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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