Chana Vinkler

916 total citations
44 papers, 618 citations indexed

About

Chana Vinkler is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Chana Vinkler has authored 44 papers receiving a total of 618 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Surgery. Recurrent topics in Chana Vinkler's work include Photosynthetic Processes and Mechanisms (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (6 papers). Chana Vinkler is often cited by papers focused on Photosynthetic Processes and Mechanisms (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (6 papers). Chana Vinkler collaborates with scholars based in Israel, United States and Germany. Chana Vinkler's co-authors include Paul D. Boyer, Dorit Lev, Michael J. Gresser, Tally Lerman‐Sagie, Akiva Apelbaum, Esther Leshinsky‐Silver, Rafi Korenstein, Mordhay Avron, G. Malinger and M. Avron and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLANT PHYSIOLOGY.

In The Last Decade

Chana Vinkler

43 papers receiving 567 citations

Peers

Countries citing papers authored by Chana Vinkler

Since Specialization

Citations

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

Fields of papers citing papers by Chana Vinkler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chana Vinkler

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Prenatal clubfoot increases the risk for clinically significant chromosomal microarray results – Analysis of 269 singleton pregnancies 2020 ·Early Human Development ·Amihood Singer, Idit Maya, Ehud Banne, Hagit Baris Feldman, Chana Vinkler, (unknown), Lena Sagi‐Dain	12
2	Severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features are due to a homozygous QARS mutation 2017 ·Neurogenetics ·Esther Leshinsky‐Silver, Jiqiang Ling, Jiang Wu, Chana Vinkler, Keren Yosovich, (unknown), (unknown), Tally Lerman‐Sagie, Dorit Lev	9
3	Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C 2016 ·European Journal of Human Genetics ·Eyal Reinstein, Ana Gutiérrez‐Fernández, Shay Tzur, Concetta Bormans, Shai Marcu, Einav Tayeb-Fligelman, Chana Vinkler, Annick Raas‐Rothschild, (unknown), Meytal Landau, Mordechai Shohat, Xosé S. Puente, Doron M. Behar, Carlos López-Otı́n	33
4	PP09.10 – 2510: A novel case of periaxin-related neuropathy associated with cataract: Expanding the clinical and molecular spectrum of perxiaxin mutation 2015 ·European Journal of Paediatric Neurology ·(unknown), Dorit Lev, Tally Lerman‐Sagie, Esther Leshinsky‐Silver, Chana Vinkler	0
5	A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features 2014 ·European Journal of Medical Genetics ·Chana Vinkler, Esther Leshinsky‐Silver, Marina Michelson, Dorothea Haas, Tally Lerman‐Sagie, Dorit Lev	2
6	Delineation of the interstitial 6q25 microdeletion syndrome: Refinement of the critical causative region 2012 ·American Journal of Medical Genetics Part A ·Marina Michelson, (unknown), Chana Vinkler, Esther Leshinsky‐Silver, (unknown), Ayala Frumkin, Sara Kivity, Tally Lerman‐Sagie, Dorit Lev	16
7	Autistic regression in a child with Silver–Russell Syndrome and maternal UPD 7 2011 ·European Journal of Paediatric Neurology ·(unknown), Michael Davidovitch, Chana Vinkler, Marina Michelson, Tally Lerman‐Sagie, Dorit Lev	1
8	Mosaic marker chromosome 16 resulting in 16q11.2–q12.1 gain in a child with intellectual disability, microcephaly, and cerebellar cortical dysplasia 2011 ·American Journal of Medical Genetics Part A ·Ayelet Zerem, Chana Vinkler, Marina Michelson, Esther Leshinsky‐Silver, Tally Lerman‐Sagie, Dorit Lev	5
9	Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother 2010 ·European Journal of Paediatric Neurology ·Marina Michelson, (unknown), Chana Vinkler, Esther Leshinsky‐Silver, (unknown), Tally Lerman‐Sagie, Dorit Lev	15
10	Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria‐polydactyly hydrocephalus syndromes 2009 ·American Journal of Medical Genetics Part A ·Karen W. Gripp, Elizabeth Hopkins, Chana Vinkler, Dorit Lev, G. Malinger, Tally Lerman‐Sagie, William B. Dobyns	29
11	Congenital Patent Ductus Venosus: An Association with the Hyper IgE Syndrome 2007 ·The Journal of Pediatrics ·(unknown), Michaela Witzling, Ilan Dalal, Chana Vinkler, (unknown), Arie Levine	8
12	A benign congenital myopathy in an inbred Samaritan family 2006 ·European Journal of Paediatric Neurology ·Dorit Lev, Menachem Sadeh, Nathan Watemberg, Ron Dabby, Chana Vinkler, (unknown), Tally Lerman‐Sagie	4
13	A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness 2004 ·Hearing Research ·Esther Leshinsky‐Silver, (unknown), Chana Vinkler, (unknown), Dorit Lev	5
14	Familial optic atrophy with white matter changes 2003 ·American Journal of Medical Genetics Part A ·Chana Vinkler, Dorit Lev, Hadas Stiebel‐Kalish, Nathan Watemberg, (unknown), Esther Leshinsky‐Silver, Tally Lerman‐Sagie	6
15	Chorionic villus sampling in multiple pregnancies 1999 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Z. Appelman, Chana Vinkler, B. Caspi	8
16	Interaction of furosemide with lipid membranes 1988 ·The Journal of Membrane Biology ·D. Bach, Chana Vinkler, I.R. Miller, S. Roy Caplan	9
17	Increased Mitochondrial DNA and RNA Polymerase Activity in Ethylene-Treated Potato Tubers 1984 ·PLANT PHYSIOLOGY ·Akiva Apelbaum, Chana Vinkler, (unknown), David R. Dilley	5
18	Partial Purification and Characterization of Arginine Decarboxylase from Avocado Fruit, A Thermostable Enzyme 1984 ·PLANT PHYSIOLOGY ·(unknown), Chana Vinkler, Akiva Apelbaum	11
19	Ethylene formation from 1‐aminocyclopropane‐1‐carboxylic acid in plant mitochondria 1983 ·FEBS Letters ·Chana Vinkler, Akiva Apelbaum	16
20	Assessment of total catalytic sites and the nature of bound nucleotide participation in photophosphorylation. 1979 ·Journal of Biological Chemistry ·(unknown), Michael J. Gresser, Chana Vinkler, Paul D. Boyer	88

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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