Samantha Stora

627 total citations
16 papers, 326 citations indexed

About

Samantha Stora is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Samantha Stora has authored 16 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Samantha Stora's work include Down syndrome and intellectual disability research (2 papers), Epigenetics and DNA Methylation (2 papers) and Lipid Membrane Structure and Behavior (2 papers). Samantha Stora is often cited by papers focused on Down syndrome and intellectual disability research (2 papers), Epigenetics and DNA Methylation (2 papers) and Lipid Membrane Structure and Behavior (2 papers). Samantha Stora collaborates with scholars based in Lebanon, France and Netherlands. Samantha Stora's co-authors include Christine Gräf, Nicole Urtz, Diana Mechtcheriakova, Frédéric Bornancin, Thomas Baumruker, Andreas Billich, André Mégarbané, Clotilde Mircher, Alexander Hoischen and Piroska Dévay and has published in prestigious journals such as Scientific Reports, Biochemical and Biophysical Research Communications and Human Molecular Genetics.

In The Last Decade

Samantha Stora

16 papers receiving 318 citations

Peers

Countries citing papers authored by Samantha Stora

Since Specialization

Citations

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

Fields of papers citing papers by Samantha Stora

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samantha Stora

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Efficacy and safety of methylphenidate on attention deficit hyperactivity disorder in children with Down syndrome 2021 ·Journal of Intellectual Disability Research ·(unknown), Clotilde Mircher, (unknown), (unknown), (unknown), Aimé Ravel, (unknown), Asma Labidi, Samantha Stora, Sophie Durand, André Mégarbané, Cécile Cieuta‐Walti	8
2	Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3 2020 ·European Journal of Medical Genetics ·(unknown), (unknown), Pratibha Nair, (unknown), Samantha Stora, Cybel Mehawej, Stephany El‐Hayek, Valérie Delague, André Mégarbané	12
3	Transcriptomic study in women with trisomy 21 identifies a possible role of the GTPases of the immunity-associated proteins (GIMAP) in the protection of breast cancer 2020 ·Scientific Reports ·André Mégarbané, David Piquemal, Anne‐Sophie Rebillat, Samantha Stora, Fabien Pierrat, (unknown), Florian Noguier, Clotilde Mircher, Aimé Ravel, (unknown), Sophie Durand, Marie‐Paule Lefranc	15
4	Report of a Second Lebanese Family with Basel-Vanagaite-Smirin-Yosef Syndrome: Possible Founder Mutation 2019 ·Molecular Syndromology ·Pratibha Nair, Sandra Sabbagh, (unknown), Florian Brunner, Samantha Stora, Mahmoud Taleb Al‐Ali, Martin Genčík, Stephany El‐Hayek, André Mégarbané	3
5	A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22) 2018 ·European Journal of Medical Genetics ·André Mégarbané, (unknown), (unknown), (unknown), Mahmoud Taleb Al‐Ali, Samantha Stora, Valérie Delague, Stephany El‐Hayek	4
6	Cornelia de Lange syndrome type 5: report of two new cases 2018 ·(unknown), (unknown), Samantha Stora, (unknown), (unknown), André Mégarbané	1
7	COQ8A and MED25 Mutations in a Child with Intellectual Disability, Microcephaly, Seizures, and Spastic Ataxia: Synergistic Effect of Digenic Variants 2018 ·Molecular Syndromology ·Pratibha Nair, (unknown), Stephany El‐Hayek, (unknown), Samantha Stora, (unknown), Mahmoud Taleb Al‐Ali, Valérie Delague, André Mégarbané	9
8	Homozygous mutation in ELMO2 may cause Ramon syndrome 2017 ·Clinical Genetics ·Cybel Mehawej, Alexander Hoischen, Roula Farah, Isabelle Marey, M David, Samantha Stora, Katherine Lachlan, Han G. Brunner, André Mégarbané	15
9	The intellectual disability of trisomy 21: differences in gene expression in a case series of patients with lower and higher IQ 2013 ·European Journal of Human Genetics ·André Mégarbané, Florian Noguier, Samantha Stora, Laurent Manchon, Clotilde Mircher, (unknown), Nathalie Dorison, Fabien Pierrat, M O Rethoré, Bernadette Trentin, Aimé Ravel, (unknown), Marie‐Paule Lefranc, David Piquemal	24
10	BDNF and DYRK1A Are Variable and Inversely Correlated in Lymphoblastoid Cell Lines from Down Syndrome Patients 2012 ·Molecular Neurobiology ·(unknown), Alexander Hoischen, (unknown), (unknown), Anne Badel, Anne Ronan, Renaud Touraine, Yann Grattau, Samantha Stora, Bregje W.M. van Bon, Bert de Vries, Björn Menten, (unknown), Jozef Gécz, Stylianos E. Antonarakis, Dominique Campion, Marie‐Claude Potier, Henri Bléhaut, Jean‐Maurice Delabar, Nathalie Janel	17
11	Trisomy for Synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes 2012 ·Human Molecular Genetics ·Jack‐Christophe Cossec, Jérémie Lavaur, Diego E. Berman, Isabelle Rivals, Alexander Hoischen, Samantha Stora, (unknown), Clotilde Mircher, Yann Grattau, Jean‐Christophe Olivo‐Marín, Fabrice de Chaumont, Magalie Lecourtois, Stylianos E. Antonarakis, Joris A. Veltman, (unknown), Charles Duyckaerts, Gilbert Di Paolo, Marie‐Claude Potier	78
12	How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability? 2011 ·American Journal of Medical Genetics Part A ·Aimé Ravel, Éliane Chouery, Samantha Stora, Nadine Jalkh, Laurent Villard, Samia A. Temtamy, André Mégarbané	6
13	A 56-year-old female patient with facio-oculo-acoustico-renal syndrome (FOAR) syndrome. Report on the natural history and of a novel mutation 2009 ·European Journal of Medical Genetics ·Samantha Stora, (unknown), Éliane Chouery, Sami Richa, Nadine Jalkh, (unknown), (unknown), André Mégarbané	6
14	Heart involvement in lamin A/C related diseases. 2006 ·PubMed ·Rabah Ben Yaou, Lucie Gueneau, L. Demay, Samantha Stora, Khadija Chikhaoui, (unknown), Gisèle Bonne	17
15	Characterization of a ceramide kinase-like protein 2004 ·Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids ·Frédéric Bornancin, Diana Mechtcheriakova, Samantha Stora, Christine Gräf, (unknown), Piroska Dévay, Nicole Urtz, Thomas Baumruker, Andreas Billich	67
16	Ceramide kinase targeting and activity determined by its N-terminal pleckstrin homology domain 2004 ·Biochemical and Biophysical Research Communications ·(unknown), Christine Gräf, Samantha Stora, Diana Mechtcheriakova, Robert Csonga, Nicole Urtz, Andreas Billich, Thomas Baumruker, Frédéric Bornancin	44

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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