Kate Pope

3.2k citations

28 papers · 867 indexed · h-index 17

Molecular Biology
Genetics top 5%
Psychiatry and Mental health top 10%
Cellular and Molecular Neuroscience
Pediatrics, Perinatology and Child Health top 10%

Co-authors: Paul J. Lockhart Richard J. Leventer David J. Amor Greta Gillies Martin B. Delatycki Melanie Bahlo Wirginia Maixner A. Simon Harvey
Topics: Genomics and Rare Diseases (6 papers)Genetics and Neurodevelopmental Disorders (6 papers)DNA Repair Mechanisms (3 papers)
Cited by: Genetics Psychiatry and Mental health Clinical Biochemistry
Journals: PLoS ONE Brain Neurology
Partner nations: Australia United States United Kingdom

In The Last Decade

Kate Pope

25 papers receiving 857 citations

Peers

Countries citing papers authored by Kate Pope

Since Specialization

Citations

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

Fields of papers citing papers by Kate Pope

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kate Pope

This figure shows the co-authorship network connecting the top 25 collaborators of Kate Pope. A scholar is included among the top collaborators of Kate Pope 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 Kate Pope. Kate Pope 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	Comprehensive Characterisation of the RFC1 Repeat in an Australian Cohort 2025 ·The Cerebellum ·(unknown),Haloom Rafehi,Liam G. Fearnley,Penny Snell,Greta Gillies,(unknown),G. Michael Hálmagyi,Kishore R. Kumar,Kate Pope,(unknown),Susan E Tomlinson,Stephen Tisch,Chi Tang,Shaun R. D. Watson,(unknown),Kathy H. C. Wu,David J. Szmulewicz,Martin B. Delatycki,Melanie Bahlo,Paul J. Lockhart	0
2	The genetic landscape and classification of infantile epileptic spasms syndrome requiring surgery due to suspected focal brain malformations 2024 ·Brain Communications ·Matthew Coleman,Min Wang,Penny Snell,(unknown),Colleen D’Arcy,(unknown),Kate Pope,Greta Gillies,Wirginia Maixner,Alison Wray,A. Simon Harvey,Cas Simons,Richard J. Leventer,Sarah Stephenson,Paul J. Lockhart,Katherine B. Howell	0
3	Rapid Diagnosis of Spinocerebellar Ataxia 36 in a Three‐Generation Family Using Short‐Read Whole‐Genome Sequencing Data 2020 ·Movement Disorders ·Haloom Rafehi,David J. Szmulewicz,Kate Pope,Mathew Wallis,John Christodoulou,Susan M. White,Martin B. Delatycki,Paul J. Lockhart,Melanie Bahlo	7
4	Genetic characterization identifies bottom-of-sulcus dysplasia as an mTORopathy 2020 ·Neurology ·(unknown),Sarah Stephenson,Kate Pope,Greta Gillies,Wirginia Maixner,(unknown),Duncan MacGregor,Colleen D’Arcy,Graeme D. Jackson,A. Simon Harvey,Richard J. Leventer,Paul J. Lockhart	30
5	Second‐hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA 2019 ·Annals of Clinical and Translational Neurology ·(unknown),Sarah Stephenson,Katherine B. Howell,Kate Pope,Greta Gillies,Alison Wray,Wirginia Maixner,Simone Mandelstam,Samuel F. Berkovic,Ingrid E. Scheffer,Duncan MacGregor,A. Simon Harvey,Paul J. Lockhart,Richard J. Leventer	55
6	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
7	‘Staying strong on the inside and outside’ to keep walking and moving around: Perspectives from Aboriginal people with Machado Joseph Disease and their families from the Groote Eylandt Archipelago, Australia 2019 ·PLoS ONE ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Kate Pope,Alan Clough,Anne Lowell,Ruth Barker	15
8	ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy 2016 ·European Heart Journal ·Dean Phelan,David J. Anderson,Sara E. Howden,Raymond C.B. Wong,Peter F. Hickey,Kate Pope,Gabrielle R. Wilson,Alice Pébay,Andrew M. Davis,Steven Petrou,Andrew G. Elefanty,Edouard G. Stanley,Paul A. James,Ivan Macciocca,Melanie Bahlo,Michael M.H. Cheung,David J. Amor,David A. Elliott,Paul J. Lockhart	38
9	Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia 2016 ·Brain ·Jijun Wan,Janos Steffen,Michael Yourshaw,Hafsa Mamsa,Erik Andersen,Sabine Rudnik‐Schöneborn,Kate Pope,Katherine B. Howell,Catriona McLean,Andrew J. Kornberg,(unknown),Paul J. Lockhart,Klaus Zerres,Monique M. Ryan,Stanley F. Nelson,Carla M. Koehler,Joanna C. Jen	69
10	The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care 2015 ·Genetics in Medicine ·Brian T. Wilson,Zornitza Stark,(unknown),Sumita Danda,Alka V. Ekbote,Solaf M. Elsayed,Louise Gibson,Judith A. Goodship,Andrew P. Jackson,(unknown),Mary D. King,Emma McCann,(unknown),(unknown),Taku Omata,Daniela T. Pilz,Kate Pope,Katsuo Sugita,Susan M. White,Ian Wilson	108
11	Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5 2015 ·Annals of Clinical and Translational Neurology ·Thomas Scerri,Jessica R. Riseley,Greta Gillies,Kate Pope,Rosemary Burgess,Simone Mandelstam,Leanne M. Dibbens,C.W. Chow,Wirginia Maixner,A. Simon Harvey,Graeme D. Jackson,David J. Amor,Martin B. Delatycki,Peter B. Crino,Samuel F. Berkovic,Ingrid E. Scheffer,Melanie Bahlo,Paul J. Lockhart,Richard J. Leventer	77
12	Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3 2015 ·Annals of Neurology ·(unknown),Thomas Scerri,Miriam Fanjul‐Fernández,Jessica R. Riseley,Greta Gillies,Kate Pope,(unknown),Julian Ik‐Tsen Heng,Simone Mandelstam,George McGillivray,Duncan MacGregor,(unknown),Wirginia Maixner,A. Simon Harvey,David J. Amor,Martin B. Delatycki,Peter B. Crino,Melanie Bahlo,Paul J. Lockhart,Richard J. Leventer	102
13	Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR 2015 ·Neurology ·Richard J. Leventer,Thomas Scerri,Ashley P.L. Marsh,Kate Pope,Greta Gillies,Wirginia Maixner,Duncan MacGregor,A. Simon Harvey,Martin B. Delatycki,David J. Amor,Peter B. Crino,Melanie Bahlo,Paul J. Lockhart	54
14	Speech and language in a genotyped cohort of individuals with Kabuki syndrome 2015 ·American Journal of Medical Genetics Part A ·Angela Morgan,Cristina Mei,(unknown),(unknown),Damien Lederer,Valérie Benoît,Margaret J. McMillin,Kati J. Buckingham,Michael J. Bamshad,Kate Pope,Susan M. White	27
15	Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency 2014 ·Orphanet Journal of Rare Diseases ·(unknown),Susan M. White,Elizabeth Fitzpatrick,Gabrielle R. Wilson,Greta Gillies,Kate Pope,Hayley S. Mountford,Pernille Mathiesen Tørring,Shane McKee,Anneke T. Vulto‐van Silfhout,Shalini N. Jhangiani,Donna M. Muzny,Richard J. Leventer,Martin B. Delatycki,David J. Amor,Paul J. Lockhart	15
16	Cauli: A Mouse Strain with an Ift140 Mutation That Results in a Skeletal Ciliopathy Modelling Jeune Syndrome 2013 ·PLoS Genetics ·Kerry A. Miller,Casey Ah-Cann,(unknown),Tiong Yang Tan,Kate Pope,Georgina Caruana,Mary‐Louise Freckmann,Ravi Savarirayan,John F. Bertram,Michael S. Dobbie,John F. Bateman,Peter G. Farlie	46
17	Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome 2013 ·European Journal of Human Genetics ·Gabrielle R. Wilson,(unknown),Katherine R. Smith,Kate Pope,Catherine Bromhead,Elizabeth Fitzpatrick,Maja Di Rocco,Maurice A. M. Van Steensel,David Coman,Richard J. Leventer,Martin B. Delatycki,David J. Amor,Melanie Bahlo,Paul J. Lockhart	30
18	Job and Career Resources: Not Just for Public Libraries 2012 ·Georgia Library Quarterly ·(unknown),Kate Pope	0
19	Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study 2012 ·Genetics in Medicine ·(unknown),Amy S. Herlihy,Charles E. Schwartz,Cindy Skinner,Minh Bui,Joanna Cobb,(unknown),David Francis,(unknown),David J. Amor,Kate Pope,(unknown),Jonathan Cohen,Jacqueline Hewitt,Randi J. Hagerman,Sylvia A. Metcalfe,John L. Hopper,Danuta Z. Loesch,Howard R. Slater,David E. Godler	18
20	Phenotypic variability of distal 22q11.2 copy number abnormalities 2011 ·American Journal of Medical Genetics Part A ·Tiong Yang Tan,Amanda Collins,Paul A. James,George McGillivray,Zornitza Stark,Christopher T. Gordon,Richard J. Leventer,Kate Pope,Robin Forbes,John A. Crolla,Devika Ganesamoorthy,Trent Burgess,Damien L. Bruno,Howard R. Slater,Peter G. Farlie,David J. Amor	54

About Kate Pope

Kate Pope is a scholar working on Library and Information Sciences, Clinical Biochemistry and Genetics, having authored 28 papers that have together received 867 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and DNA Repair Mechanisms (3 papers). The work is most often cited by research in Genetics (392 citations), Psychiatry and Mental health (147 citations) and Clinical Biochemistry (63 citations). Kate Pope has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Paul J. Lockhart, Richard J. Leventer, David J. Amor, Greta Gillies, Martin B. Delatycki, Melanie Bahlo, Wirginia Maixner, A. Simon Harvey, Duncan MacGregor and Simone Mandelstam. Their work appears in journals such as PLoS ONE, Brain and Neurology.

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