Natasha J. Brown

2.8k total citations
27 papers, 422 citations indexed

About

Natasha J. Brown is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Natasha J. Brown has authored 27 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Natasha J. Brown's work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Natasha J. Brown is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Natasha J. Brown collaborates with scholars based in Australia, United States and United Kingdom. Natasha J. Brown's co-authors include Ingrid E. Scheffer, Samuel F. Berkovic, Zornitza Stark, Tiong Yang Tan, Trent Burgess, George McGillivray, Belinda Chong, Alison Yeung, Patrick Yap and Sebastian Lunke and has published in prestigious journals such as International Journal of Molecular Sciences, Frontiers in Immunology and Journal of Medical Genetics.

In The Last Decade

Natasha J. Brown

25 papers receiving 409 citations

Peers

Countries citing papers authored by Natasha J. Brown

Since Specialization

Citations

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

Fields of papers citing papers by Natasha J. Brown

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natasha J. Brown. 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 Natasha J. Brown. The network helps show where Natasha J. Brown may publish in the future.

Co-authorship network of co-authors of Natasha J. Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Natasha J. Brown. A scholar is included among the top collaborators of Natasha J. Brown 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 Natasha J. Brown. Natasha J. Brown 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	Opportunities and challenges for paediatricians requesting funded genomic tests for children 2025 ·European Journal of Human Genetics ·Belinda McClaren, Melissa Martyn, (unknown), (unknown), Natasha J. Brown, Michael Fahey, (unknown), Clara Gaff	2
2	AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions 2025 ·American Journal of Medical Genetics Part A ·(unknown), Paul Kalitsis, (unknown), (unknown), (unknown), Florence Petit, Judith M.A. Verhagen, Alexander A.L. Jorge, Ana Cristina Victorino Krepischi, Ikeoluwa Osei‐Owusu, Emilio A. Martı́nez, Anne O’Donnell‐Luria, Nicole de Leeuw, (unknown), Ingo Helbig, David S. Francis, Natasha J. Brown	0
3	De novo enhancer deletion of LMX1B produces a mild nail‐patella clinical phenotype 2023 ·Clinical Genetics ·David Francis, (unknown), Samantha Ayres, Nicole J. Van Bergen, John Christodoulou, Natasha J. Brown, Paul Kalitsis	2
4	Improving genetic diagnostic yield in a large cohort of children with rare vascular anomalies or PIK3CA-related overgrowth spectrum 2023 ·Genetics in Medicine Open ·(unknown), (unknown), Natasha J. Brown, M. De Silva, Mark F. Bennett, (unknown), Roderic J. Phillips, Duncan MacGregor, Susan J. Robertson, Philip Bekhor, Jodie L. Simpson, Anthony Penington, Michael S. Hildebrand	0
5	Endophenotyping social cognition in the broader autism phenotype 2023 ·Autism Research ·(unknown), (unknown), Cherie Green, (unknown), Natasha J. Brown, Martin B. Delatycki, Ingrid E. Scheffer, Sarah J. Wilson	1
6	Distinct diagnostic trajectories in NBAS‐associated acute liver failure highlights the need for timely functional studies 2022 ·JIMD Reports ·Lauren Akesson, Rocío Rius, Natasha J. Brown, (unknown), (unknown), Michael Stormon, (unknown), (unknown), Yiran Guo, Håkon Håkonarson, Alison G. Compton, David R. Thorburn, (unknown), Justine E. Marum, (unknown), (unknown), Belinda Chong, Sebastian Lunke, Zornitza Stark, John Christodoulou	2
7	Virtual Reality Training in Disaster Medicine 2022 ·Simulation in Healthcare The Journal of the Society for Simulation in Healthcare ·Natasha J. Brown, (unknown), Alexander Hart, (unknown), Attila J. Hertelendy, Gregory R. Ciottone	20
8	Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome 2021 ·Molecular Case Studies ·Natasha J. Brown, Zimeng Ye, Chloe Stutterd, (unknown), Amy Schneider, Saul A. Mullen, Simone Mandelstam, Michael S. Hildebrand	3
9	Rapid Identification of Biallelic <b><i>SPTB</i></b> Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure 2020 ·Molecular Syndromology ·Christopher M. Richmond, (unknown), (unknown), Sebastian Lunke, Zornitza Stark, Amanda Moody, (unknown), Anthea Greenway, Natasha J. Brown	8
10	A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis 2019 ·European Journal of Human Genetics ·Tiong Yang Tan, Sebastian Lunke, Belinda Chong, Dean Phelan, Miriam Fanjul‐Fernández, Justine E. Marum, (unknown), Zornitza Stark, Alison Yeung, Natasha J. Brown, Chloe Stutterd, Martin B. Delatycki, Simon Sadedin, Melissa Martyn, Ilias Goranitis, Natalie Thorne, Clara Gaff, Susan M. White	35
11	Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing 2019 ·European Journal of Human Genetics ·Lauren Akesson, Stefanie Eggers, (unknown), Belinda Chong, Emma Krzesinski, Natasha J. Brown, Tiong Yang Tan, Christopher M. Richmond, David R. Thorburn, John Christodoulou, Matthew F. Hunter, Sebastian Lunke, Zornitza Stark	14
12	Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum Disorder 2019 ·Stem Cell Research ·Kiymet Bozaoglu, Yujing Gao, Edouard G. Stanley, Miriam Fanjul‐Fernández, Natasha J. Brown, Kate Pope, Cherie Green, Katerina Vlahos, Koula Sourris, Melanie Bahlo, Martin B. Delatycki, Ingrid E. Scheffer, Paul J. Lockhart	5
13	Bi-Allelic Mutations in STXBP2 Reveal a Complementary Role for STXBP1 in Cytotoxic Lymphocyte Killing 2018 ·Frontiers in Immunology ·Jamie Lopez Bernal, Tahereh Noori, Adrian Minson, (unknown), Kevin Thia, Michael S. Hildebrand, (unknown), Phillip K. Darcy, Michael H. Kershaw, Natasha J. Brown, Andrew Grigg, Joseph A. Trapani, Ilia Voskoboinik	14
14	Report of a bi-allelic truncating germline mutation in TP53 2018 ·Familial Cancer ·Natasha J. Brown, (unknown), (unknown), Susan M. White, Patrick Lo, (unknown), Victoria Beshay, Michael Sullivan, David Malkin, Jordan R. Hansford	3
15	SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia 2015 ·American Journal of Medical Genetics Part A ·Zornitza Stark, (unknown), Trent Burgess, (unknown), Alison Yeung, Tiong Yang Tan, Natasha J. Brown, Ravi Savarirayan, Neil Patel	18
16	5q31.3 Microdeletion syndrome: Clinical and molecular characterization of two further cases 2013 ·American Journal of Medical Genetics Part A ·Natasha J. Brown, Trent Burgess, Robin Forbes, George McGillivray, Andrew J. Kornberg, Simone Mandelstam, Zornitza Stark	27
17	Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families 2009 ·Journal of Medical Genetics ·Kim Hynes, Patrick Tarpey, Leanne M. Dibbens, Marta A. Bayly, Samuel F. Berkovic, Roger Smith, (unknown), Samantha J. Turner, Natasha J. Brown, (unknown), E Haan, G Turner, John Christodoulou, Helen Leonard, Deepak Gill, Michael R. Stratton, Jozef Gécz, Ingrid E. Scheffer	59
18	Vaccination, seizures and ‘vaccine damage’ 2007 ·Current Opinion in Neurology ·Natasha J. Brown, Samuel F. Berkovic, Ingrid E. Scheffer	38
19	Epistaxis in healthy children requiring hospital admission 2004 ·International Journal of Pediatric Otorhinolaryngology ·Natasha J. Brown, (unknown)	22
20	Resistance potentialities of Aedes aegypti and Culex pipiens fatigans to organophosphorus and other insecticides. 1969 ·PubMed ·(unknown), Natasha J. Brown, A. W. A. Brown	6

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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