Lisa G. Riley

2.2k citations

46 papers · 1.1k indexed · h-index 18

Co-authors: John Christodoulou David R. Thorburn Sandra T. Cooper Alison G. Compton Joëlle Rudinger‐Thirion Melanie Bahlo Minal Menezes Mark J. Cowley
Topics: Mitochondrial Function and Pathology (20 papers)Metabolism and Genetic Disorders (13 papers)RNA modifications and cancer (11 papers)
Cited by: Clinical Biochemistry Molecular Biology Genetics
Journals: PLoS ONE Analytical Biochemistry Scientific Reports
Partner nations: Australia United States France

In The Last Decade

Lisa G. Riley

44 papers receiving 1.1k citations

Peers

Countries citing papers authored by Lisa G. Riley

Since Specialization

Citations

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

Fields of papers citing papers by Lisa G. Riley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lisa G. Riley. 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 Lisa G. Riley. The network helps show where Lisa G. Riley may publish in the future.

Co-authorship network of co-authors of Lisa G. Riley

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa G. Riley. A scholar is included among the top collaborators of Lisa G. Riley 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 Lisa G. Riley. Lisa G. Riley 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	Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy 2024 ·European Journal of Human Genetics ·Lisa G. Riley,Subrata Sabui,Hamid M. Said,(unknown),Katta M. Girisha,(unknown),Sheela Nampoothiri,(unknown),Tatjana Kilo,Janine Smith,(unknown),Manoj P. Menezes,Sachin Gupta,Sandra T. Cooper,(unknown)	0
2	A founder variant expands the phenotype of WNT7B ‐related PDAC syndrome 2024 ·Clinical Genetics ·Lama AlAbdi,Zuhair Rahbeeni,Sateesh Maddirevula,(unknown),Firdous Abdulwahab,Arif O. Khan,Lisa G. Riley,Amal Alhashem,Nicolas Chassaing,Robyn V. Jamieson,Fowzan S. Alkuraya	0
3	Biallelic ATP2B1 variants as a likely cause of a novel neurodevelopmental malformation syndrome with primary hypoparathyroidism 2023 ·European Journal of Human Genetics ·(unknown),Lisa G. Riley,Purvi M. Kakadia,Stefan K. Bohlander,(unknown),(unknown),(unknown),Ian Hayes,Henry Oppermann,Cristin G. Print,Sandra T. Cooper,Polona Le Quesne Stabej	3
4	Functional interaction between compound heterozygous TERT mutations causes severe telomere biology disorder 2022 ·Blood Advances ·(unknown),(unknown),(unknown),Lucy C. Fox,Piers Blombery,Raja S. Vasireddy,Hilda A. Pickett,Julie Curtin,Pasquale Barbaro,Jonathan Rodgers,(unknown),Lisa G. Riley,Jessica K. Holien,Scott B. Cohen,Tracy M. Bryan	2
5	Biallelic pathogenic variants in COX11 are associated with an infantile‐onset mitochondrial encephalopathy 2022 ·Human Mutation ·Rocío Rius,Neal K. Bennett,Kaustuv Bhattacharya,Lisa G. Riley,Zafer Yüksel,Luke E. Formosa,Alison G. Compton,Russell C. Dale,Mark J. Cowley,Velimir Gayevskiy,(unknown),(unknown),Michael T. Ryan,David R. Thorburn,Ken Nakamura,John Christodoulou	9
6	A case of QARS1 associated epileptic encephalopathy and review of epilepsy in aminoacyl-tRNA synthetase disorders 2021 ·Brain and Development ·Denise Chan,Joëlle Rudinger‐Thirion,Magali Frugier,Lisa G. Riley,Gladys Ho,Kavitha Kothur,Shekeeb S. Mohammad	5
7	A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy 2021 ·Molecular Case Studies ·Lauren C. Briere,Melissa Walker,Frances A. High,(unknown),(unknown),(unknown),Ryosuke Ishimura,Yoshinobu Ichimura,Paul A. Caruso,Nutan Sharma,Elly Brokamp,Mary Koziura,Shekeeb S. Mohammad,Russell C. Dale,Lisa G. Riley,(unknown),John A. Phillips,Masaaki Komatsu,David A. Sweetser	15
8	A novel RLIM/RNF12 variant disrupts protein stability and function to cause severe Tonne–Kalscheuer syndrome 2021 ·Scientific Reports ·Francisco Bustos,(unknown),(unknown),Rachel Toth,Alison Eaton,Kristin D. Kernohan,Meredith Wilson,Lisa G. Riley,Greg M. Findlay	7
9	The expandingLARS2phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy 2020 ·Human Mutation ·Lisa G. Riley,Joëlle Rudinger‐Thirion,Magali Frugier,Meredith Wilson,Melissa Luig,Thushari I. Alahakoon,(unknown),Edwin P. Kirk,Tony Roscioli,Sebastian Lunke,Zornitza Stark,Klaas J. Wierenga,Sirish Palle,Maie Walsh,Emily Higgs,Susan Arbuckle,(unknown),Alison G. Compton,David R. Thorburn,John Christodoulou	18
10	The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease 2020 ·Genetics in Medicine ·Lisa G. Riley,Mark J. Cowley,Velimir Gayevskiy,André E. Minoche,Clare Puttick,David R. Thorburn,Rocío Rius,Alison G. Compton,Minal Menezes,Kaustuv Bhattacharya,David Coman,Carolyn Ellaway,Ian E. Alexander,(unknown),Maina Kava,(unknown),Carolyn M. Sue,Shanti Balasubramaniam,John Christodoulou	45
11	Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis 2018 ·The American Journal of Human Genetics ·David Coman,Lisenka E.L.M. Vissers,Lisa G. Riley,Michael Kwint,(unknown),Janet Koster,Sinje Geuer,Sarah Hopkins,(unknown),(unknown),Udo F. H. Engelke,T. Burrow,John Cardinal,James McGill,(unknown),(unknown),Hans R. Waterham,John Christodoulou,Ron A. Wevers,James Pitt	23
12	Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus–Merzbacher disease 2017 ·European Journal of Human Genetics ·(unknown),Nara Sobreira,Lisa G. Riley,Wendy Gold,Birgit Uhlenberg,Claudia Weiß,Corinne D. Boehm,Kristina Prelog,Robert Ouvrier,John Christodoulou	33
13	Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia 2015 ·Human Molecular Genetics ·Minal Menezes,Yiran Guo,Jianguo Zhang,Lisa G. Riley,Sandra T. Cooper,David R. Thorburn,Jiankang Li,Daoyuan Dong,Zhijun Li,Joseph Glessner,Ryan L. Davis,Carolyn M. Sue,Stephen I. Alexander,Susan Arbuckle,Paul Kirwan,Brendan J. Keating,Xun Xu,Håkon Håkonarson,John Christodoulou	58
14	Insights into Facebook Pages: an early adolescent health research study page targeted at parents 2015 ·International Journal of Adolescent Medicine and Health ·Krestina L. Amon,(unknown),Emily Klineberg,Lisa G. Riley,Catherine Hawke,Katharine Steinbeck	4
15	LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure 2015 ·JIMD Reports ·Lisa G. Riley,Joëlle Rudinger‐Thirion,Klaus Schmitz‐Abe,David R. Thorburn,Ryan L. Davis,Juliana Teo,Susan Arbuckle,Sandra T. Cooper,Dean R. Campagna,Magali Frugier,Kyriacos Markianos,Carolyn M. Sue,Mark D. Fleming,John Christodoulou	39
16	Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient 2014 ·PLoS ONE ·David K. Miller,Minal Menezes,Cas Simons,Lisa G. Riley,Sandra T. Cooper,Sean M. Grimmond,David R. Thorburn,John Christodoulou,Ryan J. Taft	9
17	Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect 2014 ·Neuromuscular Disorders ·Yiran Guo,Minal Menezes,Manoj P. Menezes,Jinlong Liang,Dong Li,Lisa G. Riley,Nigel F. Clarke,P. Ian Andrews,Lifeng Tian,Richard Webster,Fengxiang Wang,Xuanzhu Liu,Yulan Shen,David R. Thorburn,Brendan J. Keating,Andrew G. Engel,Håkon Håkonarson,John Christodoulou,Xun Xu	15
18	Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes 2013 ·Human Molecular Genetics ·Sze Chern Lim,(unknown),Justine E. Marum,Elena J. Tucker,Damien L. Bruno,Lisa G. Riley,John Christodoulou,Edwin P. Kirk,Avihu Boneh,(unknown),Michael Springer,Vamsi K. Mootha,Tracey A. Rouault,Silke Leimkühler,David R. Thorburn,Alison G. Compton	81
19	Lactoferrin decreases primary bovine mammary epithelial cell viability and casein expression 2008 ·Journal of Dairy Research ·Lisa G. Riley,Peter Williamson,Peter Wynn,Paul A. Sheehy	18
20	A radioassay for synaptic core complex assembly: Screening of herbal extracts for effectors 2006 ·Analytical Biochemistry ·Lisa G. Riley,Basil D. Roufogalis,George Li,Anthony S. Weiss	3

About Lisa G. Riley

Lisa G. Riley is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics, having authored 46 papers that have together received 1.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (20 papers), Metabolism and Genetic Disorders (13 papers) and RNA modifications and cancer (11 papers). The work is most often cited by research in Clinical Biochemistry (261 citations), Molecular Biology (781 citations) and Genetics (216 citations). Lisa G. Riley has collaborated with scholars based in Australia, United States and France. Frequent co-authors include John Christodoulou, David R. Thorburn, Sandra T. Cooper, Alison G. Compton, Joëlle Rudinger‐Thirion, Melanie Bahlo, Minal Menezes, Mark J. Cowley, Sze Chern Lim and Paul A. Sheehy. Their work appears in journals such as PLoS ONE, Analytical Biochemistry and Scientific Reports.

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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