Avi Saskin

667 total citations
10 papers, 67 citations indexed

About

Avi Saskin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Avi Saskin has authored 10 papers receiving a total of 67 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Pediatrics, Perinatology and Child Health and 2 papers in Surgery. Recurrent topics in Avi Saskin's work include Genomic variations and chromosomal abnormalities (2 papers), Hormonal Regulation and Hypertension (2 papers) and RNA modifications and cancer (1 paper). Avi Saskin is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), Hormonal Regulation and Hypertension (2 papers) and RNA modifications and cancer (1 paper). Avi Saskin collaborates with scholars based in Canada, United States and France. Avi Saskin's co-authors include Juan Rivera, Daniela D’Agostino, Yannis Trakadis, William D. Foulkes, Daniela Buhaş, George Chong, Anne‐Sophie Chong, Guillaume Sillon, Ceyhun Bozkurt and Céline Chéry and has published in prestigious journals such as Neurology, Human Mutation and Molecular Genetics and Metabolism.

In The Last Decade

Avi Saskin

10 papers receiving 67 citations

Peers

Countries citing papers authored by Avi Saskin

Since Specialization

Citations

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

Fields of papers citing papers by Avi Saskin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Avi Saskin

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Isolated bilateral congenital lacrimal gland agenesis—a case series 2021 ·Journal of American Association for Pediatric Ophthalmology and Strabismus ·(unknown), (unknown), Rami Darwich, Avi Saskin, Laura Russell, Christine Saint‐Martin, (unknown)	2
2	Biochemical analysis of patients with mutations in MTHFD1 and a diagnosis of methylenetetrahydrofolate dehydrogenase 1 deficiency 2020 ·Molecular Genetics and Metabolism ·Gawa Bidla, David Watkins, Céline Chéry, D. Sean Froese, (unknown), (unknown), Avi Saskin, Karen E. Christensen, Brian M. Gilfix, Jean‐Louis Guéant, David S. Rosenblatt	7
3	Reclassification of a frequent African‐origin variant from PMS2 to the pseudogene PMS2CL 2020 ·Human Mutation ·Anne‐Sophie Chong, George Chong, William D. Foulkes, Avi Saskin	8
4	PTPRD copy number variants and Ewing's sarcoma: Strengthening the association and therapeutic implications 2019 ·Cancer Genetics ·Avi Saskin, (unknown), Frédérique Tihy, Emmanuelle Lemyre, Jeffrey Davis, Fahed Halal, Linlea Armstrong	4
5	Renal tubular dysgenesis and microcolon, a novel association. Report of three cases 2018 ·European Journal of Medical Genetics ·Avi Saskin, Ahmed Alfares, Chantal Bernard, (unknown), Nancy Braverman, Indra R. Gupta, K. Bridget Brosnihan, Corinne Antignac, Marie-Claire Gübler, Vincent Morinière, Isabelle De Bie, Martin Bitzan	1
6	Glucocorticoid resistance syndrome caused by a novel <i>NR3C1</i> point mutation 2018 ·Endocrine Journal ·(unknown), Avi Saskin, (unknown), Daniela D’Agostino, Juan Rivera	20
7	COL4A1/2 CNVs and cerebral small vessel disease 2018 ·Neurology ·Avi Saskin, Guillaume Sillon, (unknown), Daniela Buhaş	6
8	Prevalence of four Mendelian disorders associated with autism in 2392 affected families 2017 ·Journal of Human Genetics ·Avi Saskin, (unknown), (unknown), Yannis Trakadis	11
9	A case of neuroblastoma in DICER1 syndrome: Chance finding or noncanonical causation? 2017 ·Pediatric Blood & Cancer ·Avi Saskin, Leanne de Kock, Nelly Sabbaghian, María Apellániz-Ruiz, Ceyhun Bozkurt, Dorothée Bouron‐Dal Soglio, William D. Foulkes	6
10	Jejunal atresia, periodic fevers and psoriatic arthropathy in Baraitser–Winter malformation syndrome 2017 ·Clinical Dysmorphology ·Avi Saskin, Marc Tischkowitz	2

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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