Aho Ilgun - Concepedia

Author

Aho Ilgun

Amsterdam UMC Location University of Amsterdam

Also Known As

A Ilgun, A. Ilgun, Aho Ilgun

Publications

500

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam University Medical Center Groningen Leiden University Medical Center Amsterdam University Medical Centers German Centre for Cardiovascular Research

About

Aho Ilgun is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	304
2	Cell Biology	2	2	65
3	Engineering	1	1	184
4	Public Health	1	1	27
5	Molecular Genetics	1	1	28

Aho Ilgun

Publications

479

Citations

H-Index

Page 1

	Year	Citations
A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation Alex V. Postma, Judith B.A. van de Meerakker, Inge B. Mathijssen, Circulation Research Systems BiologyEngineeringFamily MembersGenetic DisorderMedicine	2008	184
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 Alex V. Postma, Mariëlle Alders, Marc Sylva, Journal of Medical Genetics	2013	69
Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome Cornelis J. Boogerd, Dennis Dooijes, Aho Ilgun, Cardiovascular Research	2010	51
The Ambiguous Role of NKX2-5 Mutations in Thyroid Dysgenesis Klaartje van Engelen, Mathilda T.M. Mommersteeg, Marieke J.H. Baars, PLoS ONE Transcriptional RegulationDevelopmental BiologyGenetic DisorderLymphocyte DevelopmentGenetics	2012	43
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries Doris Škorić‐Milosavljević, Rafik Tadros, Fernanda M. Bosada, Circulation Research	2021	38
A mutation in the Kozak sequence of <i>GATA4</i> hampers translation in a family with atrial septal defects Rajiv A. Mohan, Klaartje van Engelen, Sonia Stefanovic, American Journal of Medical Genetics Part A Atrial Septal DefectCardiac MuscleCardiomyopathyDevelopmental BiologyGenetic Disorder	2014	28
Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy Najim Lahrouchi, Alex V. Postma, Christian Salazar, Journal of Clinical Investigation CardiomyopathyHeart FailureDevelopmental BiologyPld1 InhibitionCardiovascular Disease	2021	27
A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding Judith B.A. van de Meerakker, Imke Christiaans, Phil Barnett, Biochimica et Biophysica Acta (BBA) - Molecular Cell Research Cardiac MuscleCardiomyopathyMolecular PhysiologyPathologyCytoskeleton	2012	22
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot Doris Škorić‐Milosavljević, Najim Lahrouchi, Fernanda M. Bosada, Genetics in Medicine	2021	17

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