Asaf Ta‐Shma

1.7k total citations
19 papers, 988 citations indexed

About

Asaf Ta‐Shma is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Asaf Ta‐Shma has authored 19 papers receiving a total of 988 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Surgery. Recurrent topics in Asaf Ta‐Shma's work include Congenital heart defects research (7 papers), Genomics and Rare Diseases (3 papers) and Peripheral Neuropathies and Disorders (2 papers). Asaf Ta‐Shma is often cited by papers focused on Congenital heart defects research (7 papers), Genomics and Rare Diseases (3 papers) and Peripheral Neuropathies and Disorders (2 papers). Asaf Ta‐Shma collaborates with scholars based in Israel, United States and Australia. Asaf Ta‐Shma's co-authors include Orly Elpeleg, Avraham Shaag, Shamir Zenvirt, Azaria J.J.T. Rein, Zeev Perles, Simon Edvardson, Albert Taraboulos, Yuval Cinnamon, Chaim Jalas and Alexis Brice and has published in prestigious journals such as Blood, PLoS ONE and Annals of Neurology.

In The Last Decade

Asaf Ta‐Shma

19 papers receiving 983 citations

Peers

Asaf Ta‐Shma

GENET

NEURO

EPIDE

Irene Bottillo Italy

Salma M. Wakil Saudi Arabia

Dorota Monies Saudi Arabia

Mary B. Breslin United States

Pieter Faber United States

Mei Chen United States

John A. Wells United States

Yue‐Bei Luo China

Boris Keren France

Cécile Cazeneuve France

Irene Bottillo Italy

Asaf Ta‐Shma

531 ×1.2

253 ×1.1

GENET

257 ×1.3

NEURO

110 ×0.6

EPIDE

66 ×0.4

Citations per year, relative to Asaf Ta‐Shma Asaf Ta‐Shma (= 1×) peers Irene Bottillo

Countries citing papers authored by Asaf Ta‐Shma

Since Specialization

Citations

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

Fields of papers citing papers by Asaf Ta‐Shma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Asaf Ta‐Shma. 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 Asaf Ta‐Shma. The network helps show where Asaf Ta‐Shma may publish in the future.

Co-authorship network of co-authors of Asaf Ta‐Shma

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

All Works

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19 of 19 papers shown

Pagnamenta, Alistair T., Adam Jackson, Rahat Perveen, et al.. (2021). Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects. Clinical Genetics. 101(1). 127–133. 11 indexed citations

Daum, Hagit, Hagar Mor‐Shaked, Asaf Ta‐Shma, et al.. (2020). Grandparental genotyping enhances exome variant interpretation. American Journal of Medical Genetics Part A. 182(4). 689–696. 2 indexed citations

Ta‐Shma, Asaf, Tahir Naeem Khan, Asaf Vivante, et al.. (2017). Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome. The American Journal of Human Genetics. 100(4). 666–675. 18 indexed citations

Abu‐Libdeh, Bassam, Liza Douiev, Maher Shahrour, et al.. (2017). Mutation in the COX4I1 gene is associated with short stature, poor weight gain and increased chromosomal breaks, simulating Fanconi anemia. European Journal of Human Genetics. 25(10). 1142–1146. 40 indexed citations

Ta‐Shma, Asaf, Kai Zhang, Ekaterina Salimova, et al.. (2016). Congenital valvular defects associated with deleterious mutations in the PLD1 gene. Journal of Medical Genetics. 54(4). 278–286. 30 indexed citations

Mevorach, Dror, Yackov Berkun, Asaf Ta‐Shma, et al.. (2016). Therapy with eculizumab for patients with CD59 p.Cys89Tyr mutation. Annals of Neurology. 80(5). 708–717. 38 indexed citations

Perles, Zeev, Sungjin Moon, Asaf Ta‐Shma, et al.. (2015). A human laterality disorder caused by a homozygous deleterious mutation in MMP21. Journal of Medical Genetics. 52(12). 840–847. 31 indexed citations

Shamriz, Oded, Dana G. Wolf, Asaf Ta‐Shma, et al.. (2014). Hematopoietic stem cell transplantation conditioning with use of rituximab in EBV related lymphoproliferative disorders. Clinical Immunology. 151(2). 79–83. 8 indexed citations

Ta‐Shma, Asaf, Zeev Perles, Yaacov Barak, et al.. (2014). A human laterality disorder associated with a homozygous WDR16 deletion. European Journal of Human Genetics. 23(9). 1262–1265. 35 indexed citations

10.

Ta‐Shma, Asaf, Simon Edvardson, Polina Stepensky, et al.. (2014). Conotruncal malformations and absent thymus due to a deleterious NKX2-6 mutation. Journal of Medical Genetics. 51(4). 268–270. 26 indexed citations

11.

Horani, Amjad, Steven L. Brody, Thomas W. Ferkol, et al.. (2013). CCDC65 Mutation Causes Primary Ciliary Dyskinesia with Normal Ultrastructure and Hyperkinetic Cilia. PLoS ONE. 8(8). e72299–e72299. 93 indexed citations

12.

Ta‐Shma, Asaf, Ciro Leonardo Pierri, Polina Stepensky, et al.. (2013). Isolated truncus arteriosus associated with a mutation in the plexin‐D1 gene. American Journal of Medical Genetics Part A. 161(12). 3115–3120. 30 indexed citations

13.

Perles, Zeev, Amiram Nir, Sagui Gavri, et al.. (2013). Prevalence of Persistent Superior Vena Cava and Association With Congenital Heart Anomalies. The American Journal of Cardiology. 112(8). 1214–1218. 45 indexed citations

14.

Nevo, Yoram, Bruria Ben‐Zeev, Adi Tabib, et al.. (2012). CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy. Blood. 121(1). 129–135. 111 indexed citations

15.

Spiegel, Ronen, Ophry Pines, Asaf Ta‐Shma, et al.. (2012). Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2. The American Journal of Human Genetics. 90(3). 518–523. 76 indexed citations

16.

Perles, Zeev, Yuval Cinnamon, Asaf Ta‐Shma, et al.. (2012). A human laterality disorder associated with recessive CCDC11 mutation. Journal of Medical Genetics. 49(6). 386–390. 40 indexed citations

17.

Aker, Memet, Alex Rouvinski, Asaf Ta‐Shma, et al.. (2012). An SNX10 mutation causes malignant osteopetrosis of infancy. Journal of Medical Genetics. 49(4). 221–226. 78 indexed citations

18.

Edvardson, Simon, Yuval Cinnamon, Asaf Ta‐Shma, et al.. (2012). A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism. PLoS ONE. 7(5). e36458–e36458. 217 indexed citations

19.

Ta‐Shma, Asaf, et al.. (2007). Analysis of Segmental and Global Function of the Fetal Heart Using Novel Automatic Functional Imaging. Journal of the American Society of Echocardiography. 21(2). 146–150. 59 indexed citations

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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