Vahe Mokini

462 total citations
12 papers, 366 citations indexed

About

Vahe Mokini is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Vahe Mokini has authored 12 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Vahe Mokini's work include DNA Repair Mechanisms (3 papers), Carcinogens and Genotoxicity Assessment (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). Vahe Mokini is often cited by papers focused on DNA Repair Mechanisms (3 papers), Carcinogens and Genotoxicity Assessment (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). Vahe Mokini collaborates with scholars based in Albania, Italy and Tunisia. Vahe Mokini's co-authors include Bruno Dallapiccola, Berardino Porfirio, E. Gandini, Jean‐Louis Mandel, G. Alimena, G Isacchi, Massimo Pandolfo, Samir Belal, Nathalie Doerflinger and Alain Vignal and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Nephrology Dialysis Transplantation.

In The Last Decade

Vahe Mokini

12 papers receiving 351 citations

Peers

Countries citing papers authored by Vahe Mokini

Since Specialization

Citations

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

Fields of papers citing papers by Vahe Mokini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vahe Mokini

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	16P Subtelomeric Duplication With Vascular Anomalies: An Albanian Case Report And Literature Review 2012 ·SHILAP Revista de lepidopterología ·(unknown), Vahe Mokini, (unknown), (unknown), (unknown)	2
2	Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population 2011 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Stela Z. Berisha, Vahe Mokini, (unknown)	6
3	The first case of primary alpha-sarcoglycanopathy identified in Albania, in two siblings with homozygous alpha-sarcoglycan mutation. 2011 ·PubMed ·(unknown), (unknown), (unknown), (unknown), Vahe Mokini	10
4	A Pilot Beta-Thalassaemia Screening Program in the Albanian Population for a Health Planning Program 2009 ·Acta Haematologica ·(unknown), Maria Rosaria D’Apice, (unknown), Michela Biancolella, (unknown), Silvia Russo, Nicola Di Daniele, Federica Sangiuolo, Vahe Mokini, Giuseppe Novelli	6
5	Syndromic craniosynostosis due to complex chromosome 5 rearrangement andMSX2gene triplication 2007 ·American Journal of Medical Genetics Part A ·Laura Bernardini, Marco Castori, Anna Capalbo, Vahe Mokini, Rita Mingarelli, Paolo Simi, (unknown), Antonio Novelli, Bruno Dallapiccola	27
6	Identification and characterization of different SHOX gene deletions in patients with Leri–Weill dyschondrosteosys by MLPA assay 2006 ·Journal of Human Genetics ·Valentina Gatta, Ivana Antonucci, Elisena Morizio, Chiara Palka, Rita Fischetto, Vahe Mokini, (unknown), Giuseppe Calabrese, Liborio Stuppia	27
7	Brachycephalosyndactyly with ptosis, cataract, colobomas, and linear areas of skin depigmentation 1999 ·Clinical Dysmorphology ·Rita Mingarelli, Vahe Mokini, (unknown), Bruno Dallapiccola	3
8	The adolescent with acute renal failure and left ventricular hypertrophy in the absence of hypertension 1997 ·Nephrology Dialysis Transplantation ·Myftar Barbullushi, (unknown), (unknown), Alma Idrizi, (unknown), (unknown), Vahe Mokini	1
9	Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping 1993 ·Nature Genetics ·Christiane Ben Hamida, Nathalie Doerflinger, Samir Belal, (unknown), Laurence Reutenauer, Colette Dib, Gàbor Gyapay, Alain Vignal, Denis Le Paslier, Daniel Cohen, Massimo Pandolfo, Vahe Mokini, Giuseppe Novelli, F. Hentati, M. Ben Hamida, Jean‐Louis Mandel, Michel Kœnig	163
10	Analysis of 14 cystic fibrosis mutations in five South European populations 1991 ·Human Genetics ·Virginia Nunes, Paolo Gasparini, (unknown), Antonia Gaona, A. Bonizzato, Federica Sangiuolo, Angeliki Balassopoulou, (unknown), (unknown), Metka Ravnik‐Glavač, (unknown), Vahe Mokini, Radovan Komel, Bruno Dallapiccola, Pier Franco Pignatti, (unknown), Teresa Casals, Xavier Estivill	45
11	Effect of oxidants and antioxidants on chromosomal breakage in Fanconi anemia lymphocytes 1985 ·Human Genetics ·Bruno Dallapiccola, Berardino Porfirio, Vahe Mokini, G. Alimena, G Isacchi, E. Gandini	60
12	Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotes 1983 ·Human Genetics ·Berardino Porfirio, Bruno Dallapiccola, Vahe Mokini, Giuliana Alimena, E. Gandini	16

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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