Jason Pinner

2.6k total citations
23 papers, 635 citations indexed

About

Jason Pinner is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Jason Pinner has authored 23 papers receiving a total of 635 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Pediatrics, Perinatology and Child Health and 7 papers in Genetics. Recurrent topics in Jason Pinner's work include Genomics and Rare Diseases (6 papers), Metabolism and Genetic Disorders (5 papers) and Gestational Diabetes Research and Management (3 papers). Jason Pinner is often cited by papers focused on Genomics and Rare Diseases (6 papers), Metabolism and Genetic Disorders (5 papers) and Gestational Diabetes Research and Management (3 papers). Jason Pinner collaborates with scholars based in Australia, United States and United Kingdom. Jason Pinner's co-authors include Mohamed Abdellatif, Ju Lee Oei, Sara Clews, Kei Lui, Fiona J. Cooke, Glynis P. Ross, Jencia Wong, Dennis K. Yue, N. Moscow and J. Ito and has published in prestigious journals such as Diabetes Care, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Jason Pinner

22 papers receiving 604 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Jason Pinner Australia	12	266	159	153	121	100	23	635
Atıl Yüksel Türkiye	12	323 1.2×	73 0.5×	61 0.4×	95 0.8×	94 0.9×	64	559
Hoa Pham Vietnam	18	357 1.3×	51 0.3×	73 0.5×	102 0.8×	53 0.5×	43	765
Junwu Mu Japan	14	339 1.3×	63 0.4×	44 0.3×	124 1.0×	95 0.9×	18	743
Makoto Anzo Japan	18	133 0.5×	118 0.7×	147 1.0×	259 2.1×	59 0.6×	35	794
Lee A. Rigg United States	15	141 0.5×	170 1.1×	161 1.1×	49 0.4×	118 1.2×	19	907
Francesca Anna Letizia Strigini Italy	16	154 0.6×	277 1.7×	43 0.3×	36 0.3×	43 0.4×	40	726
Seiichi Fukuda Japan	19	207 0.8×	25 0.2×	70 0.5×	133 1.1×	224 2.2×	33	710
Mari Satoh Japan	16	102 0.4×	60 0.4×	140 0.9×	237 2.0×	83 0.8×	57	682
Stephanie Ryan Ireland	15	301 1.1×	24 0.2×	34 0.2×	162 1.3×	149 1.5×	50	747
Nicola Bridges United Kingdom	16	90 0.3×	126 0.8×	229 1.5×	206 1.7×	106 1.1×	41	872

Countries citing papers authored by Jason Pinner

Since Specialization

Citations

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

Fields of papers citing papers by Jason Pinner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jason Pinner

This figure shows the co-authorship network connecting the top 25 collaborators of Jason Pinner. A scholar is included among the top collaborators of Jason Pinner 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 Jason Pinner. Jason Pinner 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

Chandler, Kate, Andrew Fennell, Tzung‐Chien Hsieh, et al.. (2024). Seven Novel Variants of Weiss‐Kruszka Syndrome and Phenotype Expansion. American Journal of Medical Genetics Part A. 197(2). e63856–e63856.

Barnett, Christopher F., Mary‐Louise Freckmann, Matthew F. Hunter, et al.. (2024). Critically unwell infants and children with mitochondrial disorders diagnosed by ultrarapid genomic sequencing. Genetics in Medicine. 27(1). 101293–101293. 1 indexed citations

Ashton, Katie A., Ying Zhu, Futao Zhang, et al.. (2023). Integration of EpiSign, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re‐classification of an ARID1B missense variant. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(3). e32056–e32056. 3 indexed citations

Cardamone, Michael, et al.. (2023). Treatment of severe acute necrotizing encephalopathy of childhood with interleukin-6 receptor blockade in the first 24 h as add-on immunotherapy shows favorable long-term outcome at 2 years. Brain and Development. 45(7). 401–407. 13 indexed citations

Lim, Pei Jin, et al.. (2023). Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta. Frontiers in Endocrinology. 14. 1195704–1195704. 3 indexed citations

Goergen, Stacy, Michael Fahey, Kieran Frawley, et al.. (2021). The Fetus with Ganglionic Eminence Abnormality: Head Size and Extracranial Sonographic Findings Predict Genetic Diagnoses and Postnatal Outcomes. American Journal of Neuroradiology. 42(8). 1528–1534. 8 indexed citations

Best, Stephanie, Helen Brown, Sebastian Lunke, et al.. (2021). Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level. npj Genomic Medicine. 6(1). 5–5. 30 indexed citations

Stark, Zornitza, Amy Nisselle, Belinda McClaren, et al.. (2019). Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care. European Journal of Human Genetics. 27(10). 1493–1501. 37 indexed citations

Pinner, Jason, Cheng Yee Chan, Lucy Bowyer, et al.. (2019). Fetal diagnosis of Mowat‐Wilson syndrome by whole exome sequencing. American Journal of Medical Genetics Part A. 179(10). 2152–2157. 4 indexed citations

10.

Oates, Emily C., Sandra Coppens, Madhura Bakshi, et al.. (2018). CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES. Neuromuscular Disorders. 28. S104–S104. 1 indexed citations

11.

Pinner, Jason, et al.. (2018). Caudal regression syndrome in a fetus of a glucokinase‐maturity‐onset diabetes of the young pregnancy. Diabetic Medicine. 36(2). 252–255. 10 indexed citations

12.

Sun, Jun, Jason Pinner, Zhihui Yan, et al.. (2016). Diaphragmatic Eventration in Sisters with Asparagine Synthetase Deficiency: A Novel Homozygous ASNS Mutation and Expanded Phenotype. JIMD Reports. 34. 1–9. 23 indexed citations

13.

Duley, John A., Kevin Carpenter, Michael J. Bamshad, et al.. (2016). Elevated plasma dihydroorotate in Miller syndrome: Biochemical, diagnostic and clinical implications, and treatment with uridine. Molecular Genetics and Metabolism. 119(1-2). 83–90. 12 indexed citations

14.

Schrauwen, Isabelle, Manou Sommen, Charlotte Claes, et al.. (2013). Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. Clinical Genetics. 86(3). 282–286. 33 indexed citations

15.

Below, Jennifer E., Anita E. Beck, Heidi Gildersleeve, et al.. (2012). Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D. The American Journal of Human Genetics. 92(1). 150–156. 52 indexed citations

16.

Chakera, Ali, Sian Ellard, Jencia Wong, et al.. (2012). Antenatal Diagnosis of Fetal Genotype Determines if Maternal Hyperglycemia Due to a Glucokinase Mutation Requires Treatment. Diabetes Care. 35(9). 1832–1834. 34 indexed citations

17.

Pinner, Jason, Mary‐Louise Freckmann, Edwin P. Kirk, & Makoto Yoshino. (2010). Female heterozygotes for the hypomorphic R40H mutation can have ornithine transcarbamylase deficiency and present in early adolescence: a case report and review of the literature. Journal of Medical Case Reports. 4(1). 361–361. 8 indexed citations

18.

Numata, Sanae, Yoshiro Koda, Kenji Ihara, et al.. (2009). Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations. Journal of Human Genetics. 55(1). 18–22. 5 indexed citations

19.

Ng, Bernard, Ellie Mulyadi, J K Pereira, et al.. (2006). Familial cerebral cavernous haemangioma diagnosed in an infant with a rapidly growing cerebral lesion. Australasian Radiology. 50(6). 583–590. 13 indexed citations

20.

Abdellatif, Mohamed, Jason Pinner, Sara Clews, et al.. (2006). Effects of Breast Milk on the Severity and Outcome of Neonatal Abstinence Syndrome Among Infants of Drug-Dependent Mothers. PEDIATRICS. 117(6). e1163–e1169. 197 indexed citations

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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