Katherine Neas

1.1k total citations
22 papers, 430 citations indexed

About

Katherine Neas is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Katherine Neas has authored 22 papers receiving a total of 430 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Genetics. Recurrent topics in Katherine Neas's work include RNA modifications and cancer (4 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Katherine Neas is often cited by papers focused on RNA modifications and cancer (4 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Katherine Neas collaborates with scholars based in New Zealand, Australia and United States. Katherine Neas's co-authors include Donald R. Love, Jackie Crawford, Jonathan R. Skinner, Andrew N. Shelling, Rohan Ameratunga, See‐Tarn Woon, Andrew Aitken, Ian Hayes, Trond P. Leren and Timothy D. Koelmeyer and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Katherine Neas

22 papers receiving 427 citations

Peers

Countries citing papers authored by Katherine Neas

Since Specialization

Citations

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

Fields of papers citing papers by Katherine Neas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katherine Neas

This figure shows the co-authorship network connecting the top 25 collaborators of Katherine Neas. A scholar is included among the top collaborators of Katherine Neas 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 Katherine Neas. Katherine Neas 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	Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome 2020 ·American Journal of Medical Genetics Part A ·(unknown), Neeti Ghali, (unknown), Duncan Baker, (unknown), Angela F. Brady, Maria Luisa Giovannucci Uzielli, Cecilia Giunta, Diana Johnson, Tomoki Kosho, Katherine Neas, F M Pope, Frank Rutsch, (unknown), Glenda Sobey, Anthony Vandersteen, Fleur S. van Dijk	14
2	UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism 2020 ·The American Journal of Human Genetics ·Chunmei Li, (unknown), (unknown), Justine Rousseau, Ah Jung Heo, Katherine Neas, Brett H. Graham, Jill A. Rosenfeld, Carlos A. Bacino, Matias Wagner, (unknown), Fuad Al Mutairi, (unknown), Joseph G. Gleeson, Valentina Stanley, Maha S. Zaki, Yong Tae Kwon, Michel R. Leroux, Philippe M. Campeau	13
3	Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability 2020 ·Journal of Human Genetics ·Karen Knapp, (unknown), (unknown), Fokje Zijlstra, Hans J. C. T. Wessels, (unknown), Dirk J. Lefeber, Katherine Neas, Louise S. Bicknell	13
4	Spinocerebellar Ataxia type 29 in a family of Māori descent 2019 ·SHILAP Revista de lepidopterología ·Kathie J. Ngo, Gemma Poke, Katherine Neas, Brent L. Fogel	4
5	A pilot study of exome sequencing in a diverse New Zealand cohort with undiagnosed disorders and cancer 2018 ·Journal of the Royal Society of New Zealand ·(unknown), (unknown), Rachel Stapleton, Tim Morgan, Ian Hayes, Katherine Neas, Joanne Dixon, Kate Gibson, David Markie, Peter Tsai, Cherie Blenkiron, Sandra Fitzgerald, Paula Shields, Patrick Yap, Ben Lawrence, Cristin G. Print, Stephen P. Robertson	3
6	Currarino syndrome with two synchronous presacral teratomas 2018 ·Journal of Pediatric Surgery Case Reports ·Timothy Little, (unknown), Katherine S. Hall, (unknown), Katherine Neas, Diane Kenwright, Mark D. Stringer	3
7	Detection of sudden death syndromes in New Zealand. 2016 ·PubMed ·Nikki Earle, Jackie Crawford, Kate Gibson, Donald R. Love, Ian Hayes, Katherine Neas, Martin K. Stiles, (unknown), (unknown), Andrew Aitken, Jonathan R. Skinner	4
8	Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria 2016 ·Neuromuscular Disorders ·Gianina Ravenscroft, Nataliya Di Donato, Gabriele Hahn, Mark R. Davis, P. D. Craven, Gemma Poke, Katherine Neas, Teresa Neuhann, William B. Dobyns, Nigel G. Laing	39
9	Recurrent de novo BICD2 mutation associated with severe arthrogryposis and polymicrogyria: Expanding the phenotype 2016 ·Neuromuscular Disorders ·Gianina Ravenscroft, Nataliya Di Donato, Mark R. Davis, P. D. Craven, Gemma Poke, Katherine Neas, Teresa Neuhann, William B. Dobyns, Nigel G. Laing	1
10	Growth and Development in a Child With Resistance to Thyroid Hormone and Ectopic Thyroid Gland 2012 ·PEDIATRICS ·Natasha Heather, Kate Hall, Katherine Neas, Howard Potter, Esko Wiltshire	7
11	T‐cell acute lymphoblastic leukemia in association with Börjeson–Forssman–Lehmann syndrome due to a mutation in PHF6 2010 ·Pediatric Blood & Cancer ·(unknown), Matthew Todd, Udo Kontny, Katherine Neas, Michael Sullivan, Alasdair G. W. Hunter, David J. Picketts, Christian P. Kratz	38
12	The clinical utility of molecular diagnostic testing for primary immune deficiency disorders: a case based review 2010 ·Allergy Asthma and Clinical Immunology ·Rohan Ameratunga, See‐Tarn Woon, Katherine Neas, Donald R. Love	24
13	Posthumous diagnosis of long QT syndrome from neonatal screening cards 2010 ·Heart Rhythm ·Patrick Gladding, (unknown), Jackie Crawford, Seo‐Kyung Chung, (unknown), Dianne Webster, Katherine Neas, Donald R. Love, Mark I. Rees, Andrew N. Shelling, Jonathan R. Skinner	43
14	Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds 2010 ·Heart Rhythm ·Jonathan R. Skinner, Jackie Crawford, Warren Smith, Andrew Aitken, David Heaven, (unknown), Ian Hayes, Katherine Neas, Simon Stables, Timothy D. Koelmeyer, (unknown), (unknown), Fraser Maxwell, Kate White, Tao Yang, Dan M. Roden, Trond P. Leren, Andrew N. Shelling, Donald R. Love	121
15	Follicular Lymphoma in a X‐linked Lymphoproliferative Syndrome Carrier Female 2008 ·Scandinavian Journal of Immunology ·See‐Tarn Woon, Rohan Ameratunga, M. C. Croxson, Graeme Taylor, Katherine Neas, Edward Edkins, Peter Browett, Edward Gane, S. R. Munn	14
16	Neonatal nasal obstruction and a single maxillary central incisor 2005 ·Journal of Paediatrics and Child Health ·(unknown), Katherine Neas, Meredith Wilson, (unknown), (unknown)	7
17	Three patients with terminal deletions within the subtelomeric region of chromosome 9q 2005 ·American Journal of Medical Genetics Part A ·Katherine Neas, Janine Smith, Nicole Chia, (unknown), Luke St Heaps, Greg B. Peters, Gary F. Sholler, Dimitra Tzioumi, David Sillence, David Mowat	24
18	Novel and recurrent mutations in the C-terminal domain ofCOMP cluster in two distinct regions and result in a spectrum of phenotypes within the pseudoachondroplasia - multiple epiphyseal dysplasia disease group 2005 ·Human Mutation ·Jason Kennedy, Gail C. Jackson, (unknown), (unknown), Jordi Bella, Michael Wright, Geert Mortier, Katherine Neas, Elizabeth Thompson, Rob Elles, Michael D. Briggs	37
19	Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association 2005 ·Clinical Dysmorphology ·Katherine Neas, Greg B. Peters, (unknown), (unknown), (unknown), Jesper Brohede, Garry N. Hannan, (unknown)	3
20	A case of partial trisomy 4p syndrome presenting as severe hydronephrosis in utero 2003 ·Clinical Dysmorphology ·Katherine Neas, Nicole Chia, (unknown), Gregory B. Peters, Lesley C. Adès	1

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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