Aho Ilgun

505 total citations
9 papers, 252 citations indexed

About

Aho Ilgun is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Aho Ilgun has authored 9 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Epidemiology and 2 papers in Genetics. Recurrent topics in Aho Ilgun's work include Congenital heart defects research (6 papers), Congenital Heart Disease Studies (5 papers) and Electric Motor Design and Analysis (2 papers). Aho Ilgun is often cited by papers focused on Congenital heart defects research (6 papers), Congenital Heart Disease Studies (5 papers) and Electric Motor Design and Analysis (2 papers). Aho Ilgun collaborates with scholars based in Netherlands, United States and Switzerland. Aho Ilgun's co-authors include Alex V. Postma, Phil Barnett, Vincent M. Christoffels, Jan Lam, Inge B. Mathijssen, Arthur A.M. Wilde, Ronald H. Lekanne Deprez, Antoon F.M. Moorman, Antoon F.M. Moorman and Klaartje van Engelen and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Circulation Research.

In The Last Decade

Aho Ilgun

8 papers receiving 251 citations

Peers

Aho Ilgun

MB

CCM

EPIDE

GENET

PRM

Darroch Hall United Kingdom

Ruo-Gu Li China

Kamel Shibbani United States

Yu‐Min Sun China

Jesper R. Gådin Sweden

Maren Sitte Germany

Elise Glen United Kingdom

Bo Wen Cai China

Alessandra Fornaro Italy

Paula Fernández‐Álvarez Spain

Darroch Hall United Kingdom

Aho Ilgun

148 ×0.8

MB

53 ×0.6

CCM

80 ×1.2

EPIDE

81 ×1.4

GENET

54 ×1.8

PRM

Citations per year, relative to Aho Ilgun Aho Ilgun (= 1×) peers Darroch Hall

Countries citing papers authored by Aho Ilgun

Since Specialization

Citations

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

Fields of papers citing papers by Aho Ilgun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aho Ilgun

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

All Works

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9 of 9 papers shown

1.

Alaamery, Manal, Nour Albesher, Fahad Alhabshan, et al.. (2023). TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy. Journal of Cardiovascular Development and Disease. 10(11). 455–455. 1 indexed citations

2.

Postma, Alex V., Christina Rapp, Katrin Knoflach, et al.. (2023). Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension. SHILAP Revista de lepidopterología. 1(1). 100811–100811. 1 indexed citations

3.

Mohan, Rajiv A., Klaartje van Engelen, Sonia Stefanovic, et al.. (2014). A mutation in the Kozak sequence of GATA4 hampers translation in a family with atrial septal defects. American Journal of Medical Genetics Part A. 164(11). 2732–2738. 18 indexed citations

4.

Postma, Alex V., Mariëlle Alders, Marc Sylva, et al.. (2013). Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal. Journal of Medical Genetics. 51(2). 90–97. 33 indexed citations

5.

Christiaans, Imke, Phil Barnett, Ronald H. Lekanne Deprez, et al.. (2012). A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1833(4). 833–839. 15 indexed citations

6.

Engelen, Klaartje van, Mathilda T.M. Mommersteeg, Marieke J.H. Baars, et al.. (2012). The Ambiguous Role of NKX2-5 Mutations in Thyroid Dysgenesis. PLoS ONE. 7(12). e52685–e52685. 27 indexed citations

7.

Boogerd, Cornelis J., Dennis Dooijes, Aho Ilgun, et al.. (2011). Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010). Cardiovascular Research. 89(1).

8.

Boogerd, Cornelis J., Dennis Dooijes, Aho Ilgun, et al.. (2010). Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome. Cardiovascular Research. 88(1). 130–139. 34 indexed citations

9.

Postma, Alex V., Inge B. Mathijssen, Phil Barnett, et al.. (2008). A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation. Circulation Research. 102(11). 1433–1442. 123 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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