Kristi Jones

3.9k total citations
37 papers, 790 citations indexed

About

Kristi Jones is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Kristi Jones has authored 37 papers receiving a total of 790 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 13 papers in Genetics and 7 papers in Genetics. Recurrent topics in Kristi Jones's work include Muscle Physiology and Disorders (13 papers), Neurogenetic and Muscular Disorders Research (12 papers) and RNA modifications and cancer (5 papers). Kristi Jones is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Neurogenetic and Muscular Disorders Research (12 papers) and RNA modifications and cancer (5 papers). Kristi Jones collaborates with scholars based in Australia, United States and France. Kristi Jones's co-authors include Kathryn N. North, Sandra T. Cooper, Michelle A. Farrar, Leigh B. Waddell, Mark R. Davis, David Mowat, Daniel G. MacArthur, Nigel G. Laing, Kate A. Carey and Nigel F. Clarke and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Clinical Cancer Research.

In The Last Decade

Kristi Jones

35 papers receiving 776 citations

Peers

Countries citing papers authored by Kristi Jones

Since Specialization

Citations

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

Fields of papers citing papers by Kristi Jones

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristi Jones

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Newborn screening for Duchenne muscular dystrophy: the perspectives of stakeholders 2024 ·The Lancet Regional Health - Western Pacific ·(unknown), Didu Kariyawasam, Hugo Sampaio, (unknown), Kristi Jones, Michelle A. Farrar	1
2	Can postural changes in spirometry in children with Duchenne muscular dystrophy predict sleep hypoventilation? 2023 ·Paediatric Respiratory Reviews ·(unknown), (unknown), Karen A. Waters, Helen Young, Kristi Jones, Dominic A. Fitzgerald	1
3	The Carrier Frequency of Two SMN1 Genes in Parents of Symptomatic Children with SMA and the Significance of SMN1 Exon 8 in Carriers 2023 ·Genes ·(unknown), (unknown), (unknown), David Mowat, Kristi Jones, Edwin P. Kirk, Didu Kariyawasam, Michelle A. Farrar, Arlene D’Silva	1
4	The relationship between beta-ureidopropionase deficiency due to UPB1 variants and human phenotypes is uncertain 2022 ·Molecular Genetics and Metabolism ·(unknown), Richard J. N. Allcock, Joy Yaplito‐Lee, (unknown), Carolyn Ellaway, Kristi Jones, Arthavan Selvanathan, Janice M. Fletcher, James Pitt, André B. P. Kuilenburg, Martin B. Delatycki, Nigel G. Laing, Edwin P. Kirk	2
5	Incidence of Duchenne muscular dystrophy in the modern era; an Australian study 2022 ·European Journal of Human Genetics ·Didu Kariyawasam, Arlene D’Silva, David Mowat, (unknown), Hugo Sampaio, Kristi Jones, Peter J. Taylor, Michelle A. Farrar	17
6	AIM™ platform: A new immunotherapy approach for viral diseases 2022 ·Frontiers in Medicine ·(unknown), Ruipeng Wang, (unknown), (unknown), Alison Farrell, C. E. Johnson, Adam R. Parks, (unknown), (unknown), Sojung Kim, Kristi Jones, Mathias Oelke, Jerome B. Zeldis	2
7	L‐carnitine supplementation for muscle weakness and fatigue in children with neurofibromatosis type 1: A Phase 2a clinical trial 2021 ·American Journal of Medical Genetics Part A ·(unknown), Joshua Burns, Paula Bray, (unknown), Anita J. Mudge, Kristi Jones, Matthew A. Summers, Andrew Biggin, Craig F. Munns, Marnee J. McKay, Jennifer Baldwin, David G. Little, Aaron Schindeler	12
8	Effect of a multicomponent nutritional supplement on functional outcomes for Duchenne muscular dystrophy: A randomized controlled trial 2021 ·Clinical Nutrition ·Zoe E. Davidson, Ian Hughes, Monique M. Ryan, Andrew J. Kornberg, Anita Cairns, Kristi Jones, (unknown), Hugo Sampaio, (unknown), Helen Truby	7
9	Rapid Expansion of Highly Functional Antigen-Specific T Cells from Patients with Melanoma by Nanoscale Artificial Antigen-Presenting Cells 2020 ·Clinical Cancer Research ·Junya Ichikawa, Tatsuya Yoshida, Ariel Isser, Andressa S. Laino, Melinda Vassallo, David Woods, Sojung Kim, Mathias Oelke, Kristi Jones, Jonathan P. Schneck, Jeffrey S. Weber	34
10	AIM Platform: A Novel Nano Artificial Antigen-Presenting Cell-Based Clinical System Designed to Consistently Produce Multi-Antigen-Specific T-Cell Products with Potent and Durable Anti-Tumor Properties 2020 ·Transfusion Medicine and Hemotherapy ·(unknown), Ruipeng Wang, (unknown), Daniel P. Bednarik, Han Myint, Kristi Jones, Mathias Oelke	7
11	Importance of muscle biopsy to establish pathogenicity of DMD missense and splice variants 2019 ·Neuromuscular Disorders ·Hannah Jones, Samantha J. Bryen, Leigh B. Waddell, Adam Bournazos, Mark R. Davis, Michelle A. Farrar, Catriona McLean, David Mowat, Hugo Sampaio, Ian Woodcock, Monique M. Ryan, Kristi Jones, Sandra T. Cooper	11
12	Nusinersen for SMA: expanded access programme 2018 ·Journal of Neurology Neurosurgery & Psychiatry ·Michelle A. Farrar, (unknown), Kate A. Carey, Anita Cairns, Robin Forbes, (unknown), (unknown), Kristi Jones, Manoj P. Menezes, (unknown), (unknown), (unknown), Richard Webster, Ian Woodcock, Eppie M. Yiu, Hugo Sampaio, Monique M. Ryan	50
13	New and developing therapies in spinal muscular atrophy 2018 ·Paediatric Respiratory Reviews ·Didu Kariyawasam, Kate A. Carey, Kristi Jones, Michelle A. Farrar	23
14	Can daytime measures of lung function predict respiratory failure in children with neuromuscular disease? 2015 ·Paediatric Respiratory Reviews ·(unknown), Karen A. Waters, Kristi Jones, Helen Young, Dominic A. Fitzgerald	1
15	Chronic urticaria of neonatal onset: A potential sign of autoinflammation 2010 ·Journal of Paediatrics and Child Health ·Sam Mehr, Kristi Jones, Davinder Singh‐Grewal, Ivona Aksentijevich, Alyson Kakakios	4
16	Mutations in Contactin-1, a Neural Adhesion and Neuromuscular Junction Protein, Cause a Familial Form of Lethal Congenital Myopathy 2008 ·The American Journal of Human Genetics ·Alison G. Compton, Douglas E. Albrecht, Jane T. Seto, Sandra T. Cooper, Biljana Ilkovski, Kristi Jones, Daniel Challis, David Mowat, Barbara Ranscht, Melanie Bahlo, Stanley C. Froehner, Kathryn N. North	61
17	Variable penetrance of COL6A1 null mutations: Implications for prenatal diagnosis and genetic counselling in Ullrich congenital muscular dystrophy families 2007 ·Neuromuscular Disorders ·Rachel A. Peat, Naomi L. Baker, Kristi Jones, Kathryn N. North, Shireen R. Lamandé	30
18	Juvenile Huntington disease 2006 ·Journal of Paediatrics and Child Health ·Nimeshan Geevasinga, (unknown), Kristi Jones, Monique M. Ryan	19
19	A girl with duplication 17p10‐p12 associated with a dicentric chromosome 2003 ·American Journal of Medical Genetics Part A ·Christine J. Shaw, Paweł Stankiewicz, John Christodoulou, (unknown), Kristi Jones, James R. Lupski	8
20	Deficiency of the syntrophins and α-dystrobrevin in patients with inherited myopathy 2003 ·Neuromuscular Disorders ·Kristi Jones, Alison G. Compton, Nan Yang, (unknown), Matthew F. Peters, David Mowat, Louis M. Kunkel, Stanley C. Froehner, Kathryn N. North	23

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.

Explore authors with similar magnitude of impact