Hannah Vanyai

1.7k total citations
24 papers, 762 citations indexed

About

Hannah Vanyai is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Hannah Vanyai has authored 24 papers receiving a total of 762 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Hannah Vanyai's work include Congenital heart defects research (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Epigenetics and DNA Methylation (4 papers). Hannah Vanyai is often cited by papers focused on Congenital heart defects research (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Epigenetics and DNA Methylation (4 papers). Hannah Vanyai collaborates with scholars based in Australia, United Kingdom and United States. Hannah Vanyai's co-authors include Anne K. Voss, Tim Thomas, Bilal N. Sheikh, Andreas Strasser, Stephanie Grabow, Carl W. White, Francine Ke, Kevin D. G. Pfleger, Lachlan Whitehead and Peter E. Czabotar and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Hannah Vanyai

23 papers receiving 757 citations

Peers

Countries citing papers authored by Hannah Vanyai

Since Specialization

Citations

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

Fields of papers citing papers by Hannah Vanyai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hannah Vanyai

This figure shows the co-authorship network connecting the top 25 collaborators of Hannah Vanyai. A scholar is included among the top collaborators of Hannah Vanyai 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 Hannah Vanyai. Hannah Vanyai 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	Transcriptomic changes including p53 dysregulation prime DNMT3A mutant cells for transformation 2025 ·EMBO Reports ·(unknown), (unknown), Andrew J. Kueh, Martin Pál, Lin Tai, Alexandra L. Garnham, Connie S.N. Li Wai Suen, Hannah Vanyai, Quentin Gouil, James Lancaster, Sylvie Callegari, (unknown), Elizabeth Lieschke, (unknown), Andreas Strasser, Yang Liao, Shi Wei, Andrew H. Wei, Marco J. Herold	0
2	KAT6B overexpression in mice causes aggression, anxiety, and epilepsy 2025 ·iScience ·Maria Bergamasco, Ezgi Öztürk, Pablo M. Casillas‐Espinosa, Alexandra L. Garnham, Waruni Abeysekera, Verena C. Wimmer, Pradeep Rajasekhar, Hannah Vanyai, Lachlan Whitehead, Marnie E. Blewitt, Kelly L. Rogers, Adam P. Vogel, Anthony J. Hannan, Gordon K. Smyth, Nigel C. Jones, Tim Thomas, Anne K. Voss	1
3	Increasing histone acetylation improves sociability and restores learning and memory in KAT6B-haploinsufficient mice 2024 ·Journal of Clinical Investigation ·Maria Bergamasco, Hannah Vanyai, Alexandra L. Garnham, Niall D. Geoghegan, Adam P. Vogel, (unknown), Kelly L. Rogers, Gordon K. Smyth, Marnie E. Blewitt, Anthony J. Hannan, Tim Thomas, Anne K. Voss	9
4	ING4 and ING5 are essential for histone H3 lysine 14 acetylation and epicardial cell lineage development 2024 ·Development ·(unknown), Hannah Vanyai, Connie S.N. Li Wai Suen, Alexandra L. Garnham, (unknown), Maria Bergamasco, (unknown), Stephen Wilcox, Christine Biben, Gordon K. Smyth, Tim Thomas, Anne K. Voss	4
5	Slc35a2 mosaic knockout impacts cortical development, dendritic arborisation, and neuronal firing 2024 ·Neurobiology of Disease ·(unknown), (unknown), Hannah Vanyai, Richard J. Leventer, Snezana Maljevic, Paul J. Lockhart, Katherine B. Howell, Christopher A. Reid	9
6	The chromatin reader protein ING5 is required for normal hematopoietic cell numbers in the fetal liver 2023 ·Frontiers in Immunology ·(unknown), Hannah Vanyai, Yuqing Yang, Anne K. Voss, Tim Thomas	3
7	Control of skeletal morphogenesis by the Hippo-YAP/TAZ pathway 2020 ·Development ·Hannah Vanyai, Fabrice Prin, (unknown), N. Bishara Marzook, Stefan Boeing, (unknown), Rebecca E. Saunders, Thomas J. Snoeks, Michael Howell, Timothy J. Mohun, Barry J. Thompson	39
8	CRISPR-Mediated Protein Tagging with Nanoluciferase to Investigate Native Chemokine Receptor Function and Conformational Changes 2020 ·Cell chemical biology ·Carl W. White, (unknown), Hannah Vanyai, Kevin D. G. Pfleger, Stephen J. Hill	48
9	A citizen science model for implementing statewide educational DNA barcoding 2019 ·PLoS ONE ·(unknown), Frazer Thorpe, Christopher B. Gorman, (unknown), Gorjana Robevska, (unknown), (unknown), Hannah Vanyai, (unknown), Kirby Siemering, Joanna Sumner	8
10	Enigma proteins regulate YAP mechanotransduction 2018 ·Journal of Cell Science ·Ahmed Elbediwy, Hannah Vanyai, María-del-Carmen Díaz-de-la-Loza, David Frith, Ambrosius P. Snijders, Barry J. Thompson	42
11	YAP drives cutaneous squamous cell carcinoma formation and progression 2018 ·eLife ·Zoé I. Vincent‐Mistiaen, Ahmed Elbediwy, Hannah Vanyai, Jennifer L. Cotton, Gordon Stamp, Emma Nye, Bradley Spencer‐Dene, Gareth J. Thomas, Junhao Mao, Barry J. Thompson	44
12	Subtle Changes in the Levels of BCL-2 Proteins Cause Severe Craniofacial Abnormalities 2018 ·Cell Reports ·Stephanie Grabow, Andrew J. Kueh, Francine Ke, Hannah Vanyai, Bilal N. Sheikh, Michael A. Dengler, (unknown), (unknown), Ian Smyth, Lynelle K. Jones, Frédéric J. de Sauvage, Mark Scott, Lachlan Whitehead, Anne K. Voss, Andreas Strasser	29
13	Embryogenesis and Adult Life in the Absence of Intrinsic Apoptosis Effectors BAX, BAK, and BOK 2018 ·Cell ·Francine Ke, Hannah Vanyai, Angus D. Cowan, Alex R. D. Delbridge, Lachlan Whitehead, Stephanie Grabow, Peter E. Czabotar, Anne K. Voss, Andreas Strasser	155
14	Using nanoBRET and CRISPR/Cas9 to monitor proximity to a genome-edited protein in real-time 2017 ·Scientific Reports ·Carl W. White, Hannah Vanyai, Heng B. See, Elizabeth K. M. Johnstone, Kevin D. G. Pfleger	45
15	De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation 2016 ·Cell Reports ·Matilda Haas, Linh Ngo, Shanshan Li, Sibylle Schleich, Zhengdong Qu, Hannah Vanyai, (unknown), (unknown), Ivan Gladwyn‐Ng, Alistair T. Pagnamenta, Jenny C. Taylor, Helen Stewart, Usha Kini, Kent E. Duncan, Aurelio A. Teleman, David A. Keays, Julian Ik‐Tsen Heng	26
16	Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons 2016 ·Neural Development ·Ivan Gladwyn‐Ng, Lieven Huang, Linh Ngo, Shanshan Li, Zhengdong Qu, Hannah Vanyai, (unknown), John M. Davis, Julian Ik‐Tsen Heng	27
17	Infantile Neurodegenerative Disorder Associated with Mutations inTBCD, an Essential Gene in the Tubulin Heterodimer Assembly Pathway 2016 ·Human Molecular Genetics ·Simon Edvardson, Guoling Tian, (unknown), Hannah Vanyai, Linh Ngo, Saiuj Bhat, Adi Aran, (unknown), (unknown), Bassam Abu‐Libdeh, Nicholas J. Cowan, Julian Ik‐Tsen Heng, Orly Elpeleg	21
18	The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome 2016 ·Scientific Reports ·Shanshan Li, Zhengdong Qu, Matilda Haas, Linh Ngo, You Jeong Heo, Hyo Jung Kang, Joanne M. Britto, (unknown), Hannah Vanyai, Seong‐Seng Tan, Tailoi Chan‐Ling, Jenny M. Gunnersen, Julian Ik‐Tsen Heng	15
19	Mesodermal expression of Moz is necessary for cardiac septum development 2015 ·Developmental Biology ·Hannah Vanyai, Tim Thomas, Anne K. Voss	22
20	MOZ (MYST3, KAT6A) inhibits senescence via the INK4A-ARF pathway 2015 ·Oncogene ·Bilal N. Sheikh, Belinda Phipson, Farrah El-Saafin, Hannah Vanyai, Natalie L. Downer, Matthew Bird, Andrew J. Kueh, Rose E. May, Gordon K. Smyth, Anne K. Voss, Tim Thomas	63

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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