Lachlan A. Jolly

2.3k total citations
29 papers, 1.2k citations indexed

About

Lachlan A. Jolly is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Lachlan A. Jolly has authored 29 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 18 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Lachlan A. Jolly's work include Genetics and Neurodevelopmental Disorders (17 papers), Ubiquitin and proteasome pathways (11 papers) and RNA modifications and cancer (5 papers). Lachlan A. Jolly is often cited by papers focused on Genetics and Neurodevelopmental Disorders (17 papers), Ubiquitin and proteasome pathways (11 papers) and RNA modifications and cancer (5 papers). Lachlan A. Jolly collaborates with scholars based in Australia, United States and United Kingdom. Lachlan A. Jolly's co-authors include Jozef Gécz, Stephen A. Wood, Mariyam Murtaza, Claire C. Homan, Simon C. Barry, Rachael Z. Murray, R. Jacob, Raman Kumar, Verdon Taylor and Paul Q. Thomas and has published in prestigious journals such as Neuron, PLoS ONE and Scientific Reports.

In The Last Decade

Lachlan A. Jolly

28 papers receiving 1.2k citations

Peers

Countries citing papers authored by Lachlan A. Jolly

Since Specialization

Citations

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

Fields of papers citing papers by Lachlan A. Jolly

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lachlan A. Jolly. 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 Lachlan A. Jolly. The network helps show where Lachlan A. Jolly may publish in the future.

Co-authorship network of co-authors of Lachlan A. Jolly

This figure shows the co-authorship network connecting the top 25 collaborators of Lachlan A. Jolly. A scholar is included among the top collaborators of Lachlan A. Jolly 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 Lachlan A. Jolly. Lachlan A. Jolly 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	Genetic disruption of nonsense-mediated mRNA decay in neurodevelopmental disorders 2025 ·Current Opinion in Genetics & Development ·(unknown), Lachlan A. Jolly	0
2	Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway 2024 ·Molecular Psychiatry ·(unknown), Alison Gardner, Clare L. van Eyk, (unknown), Paul Q. Thomas, (unknown), Lachlan A. Jolly, Isabel Martínez‐Garay, (unknown), Karthik Shantharam Kamath, Raman Kumar, Jozef Gécz	4
3	Endogenous protein interactomes resolved through immunoprecipitation-coupled quantitative proteomics in cell lines 2022 ·STAR Protocols ·Raman Kumar, Karthik Shantharam Kamath, Luke Carroll, Peter Hoffmann, Jozef Gécz, Lachlan A. Jolly	4
4	The DUB Club: Deubiquitinating Enzymes and Neurodevelopmental Disorders 2022 ·Biological Psychiatry ·Lachlan A. Jolly, Raman Kumar, Peter Penzes, Michael Piper, Jozef Gécz	16
5	Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells 2021 ·Molecular Genetics and Metabolism Reports ·(unknown), Lachlan A. Jolly, Brett V. Johnson, Megan S. Lord, Ha Na Kim, Jennifer T. Saville, Maria Fuller, Sharon Byers, Ainslie L.K. Derrick‐Roberts	4
6	Abnormal Behavior and Cortical Connectivity Deficits in Mice Lacking Usp9x 2020 ·Cerebral Cortex ·(unknown), (unknown), Nyoman D. Kurniawan, Oressia Zalucki, (unknown), Lachlan A. Jolly, Thomas H.J. Burne, Stephen A. Wood, Michael Piper	6
7	Robust imaging and gene delivery to study human lymphoblastoid cell lines 2018 ·Journal of Human Genetics ·Lachlan A. Jolly, Ying Sun, Renée Carroll, Claire C. Homan, Jozef Gécz	1
8	Viperin is an important host restriction factor in control of Zika virus infection 2017 ·Scientific Reports ·Kylie H. Van der Hoek, Nicholas S. Eyre, (unknown), (unknown), (unknown), Jillian M. Carr, Matthew J. Gartner, Lachlan A. Jolly, Paul Q. Thomas, Fatwa Adikusuma, Tanja Jankovic‐Karasoulos, Claire T. Roberts, Karla J. Helbig, Michael R. Beard	90
9	Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors 2017 ·Scientific Reports ·(unknown), Mariyam Murtaza, Nicholas Matigian, Lachlan A. Jolly, Stephen A. Wood	24
10	Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis 2017 ·Translational Psychiatry ·(unknown), Matilda R. Jackson, Shervi Lie, Lachlan A. Jolly, Michael Field, Simon C. Barry, Victoria L. Harvey, Cheryl Shoubridge	29
11	USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitors 2017 ·Scientific Reports ·(unknown), (unknown), (unknown), Devathri Nanayakkara, Bernadette Bellette, (unknown), Deepti Domingo, Jozef Gécz, Mariyam Murtaza, Lachlan A. Jolly, Stephen A. Wood	34
12	Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice 2016 ·Scientific Reports ·Daniel T. Pederick, Claire C. Homan, Emily J. Jaehne, Sandra Piltz, Bryan P. Haines, Bernhard T. Baune, Lachlan A. Jolly, (unknown), Jozef Gécz, Paul Q. Thomas	44
13	La FAM fatale: USP9X in development and disease 2015 ·Cellular and Molecular Life Sciences ·Mariyam Murtaza, Lachlan A. Jolly, Jozef Gécz, Stephen A. Wood	142
14	Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth 2014 ·The American Journal of Human Genetics ·Claire C. Homan, Raman Kumar, Lam Son Nguyen, Eric Haan, F. Lucy Raymond, Fatima Abidi, Martine Raynaud, Charles E. Schwartz, Stephen A. Wood, Jozef Gécz, Lachlan A. Jolly	100
15	The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth 2013 ·Human Molecular Genetics ·Lachlan A. Jolly, Claire C. Homan, R. Jacob, Simon C. Barry, Jozef Gécz	95
16	Loss of Usp9x Disrupts Cortical Architecture, Hippocampal Development and TGFβ-Mediated Axonogenesis 2013 ·PLoS ONE ·Shane Stegeman, Lachlan A. Jolly, (unknown), Jozef Gécz, Linda J. Richards, Alan Mackay‐Sim, Stephen A. Wood	62
17	Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disability 2013 ·Human Molecular Genetics ·Mireille Melko, Lam Son Nguyen, Marie Shaw, Lachlan A. Jolly, Barbara Bardoni, Jozef Gécz	10
18	A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability 2012 ·The American Journal of Human Genetics ·Lingli Huang, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, Alison Gardner, Raman Kumar, Evelyn Douglas, Cheryl Shoubridge, Dagmar Wieczorek, Andreas Tzschach, Monika Cohen, Anna Hackett, Michael Field, Guy Froyen, Hao Hu, Stefan A. Haas, Hans‐Hilger Ropers, Vera M. Kalscheuer, Mark Corbett, Jozef Gécz	73
19	USP9X Enhances the Polarity and Self-Renewal of Embryonic Stem Cell-derived Neural Progenitors 2009 ·Molecular Biology of the Cell ·Lachlan A. Jolly, Verdon Taylor, Stephen A. Wood	48
20	The FAM Deubiquitylating Enzyme Localizes to Multiple Points of Protein Trafficking in Epithelia, where It Associates with E-cadherin and β-catenin 2004 ·Molecular Biology of the Cell ·Rachael Z. Murray, Lachlan A. Jolly, Stephen A. Wood	69

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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