Kerry A. Miller

1.7k total citations
24 papers, 507 citations indexed

About

Kerry A. Miller is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Kerry A. Miller has authored 24 papers receiving a total of 507 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Sensory Systems. Recurrent topics in Kerry A. Miller's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Hedgehog Signaling Pathway Studies (4 papers) and Congenital heart defects research (3 papers). Kerry A. Miller is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Hedgehog Signaling Pathway Studies (4 papers) and Congenital heart defects research (3 papers). Kerry A. Miller collaborates with scholars based in Australia, United Kingdom and Netherlands. Kerry A. Miller's co-authors include Gary W. Gill, J K Frost, Hans‐Henrik M. Dahl, Alasdair MacKenzie, Louise H. Williams, Shehnaaz S.M. Manji, Scott Davidson, J. Martin Collinson, Peter G. Farlie and Melanie Bahlo and has published in prestigious journals such as Bioinformatics, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Kerry A. Miller

24 papers receiving 494 citations

Peers

Countries citing papers authored by Kerry A. Miller

Since Specialization

Citations

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

Fields of papers citing papers by Kerry A. Miller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kerry A. Miller. 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 Kerry A. Miller. The network helps show where Kerry A. Miller may publish in the future.

Co-authorship network of co-authors of Kerry A. Miller

This figure shows the co-authorship network connecting the top 25 collaborators of Kerry A. Miller. A scholar is included among the top collaborators of Kerry A. Miller 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 Kerry A. Miller. Kerry A. Miller 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	BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome 2024 ·Journal of Medical Genetics ·Kerry A. Miller, David A. Cruz Walma, Daniel M. Pinkas, (unknown), Joshua C. Bufton, William Richardson, (unknown), Alice E. Hunt, (unknown), Verity Hartill, Michael Parker, Simon J. McGowan, Stephen R.F. Twigg, R. Chalk, David Staunton, David Johnson, Andrew O.M. Wilkie, Alex N. Bullock	5
2	amplimap: a versatile tool to process and analyze targeted NGS data 2019 ·Bioinformatics ·Nils Koelling, Marie Bernkopf, Eduardo Calpena, Geoffrey J. Maher, Kerry A. Miller, H. Ralph, Anne Goriely, Andrew O.M. Wilkie	4
3	A dominant-negative mutation in the BTB domain of KCTD15 in a family with frontal lipoma, congenital heart disease and cutis aplasia of the scalp defines a novel syndrome 2018 ·European Journal of Human Genetics ·Kerry A. Miller, (unknown), Joshua C. Bufton, (unknown), Simon J. McGowan, M. Parker, (unknown), Alex N. Bullock, (unknown)	1
4	Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability 2015 ·The American Journal of Human Genetics ·Stephen R.F. Twigg, (unknown), Jacqueline A.C. Goos, (unknown), A. Jeannette M. Hoogeboom, Ans M.W. van den Ouweland, Sigrid M. A. Swagemakers, Maarten H. Lequin, (unknown), Simon J. McGowan, (unknown), Kerry A. Miller, Steven A. Wall, Peter J. van der Spek, Irene M.J. Mathijssen, Erwin Pauws, Christa Merzdorf, Andrew O.M. Wilkie	43
5	Olfr603, an orphan olfactory receptor, is expressed in multiple specific embryonic tissues 2015 ·Gene Expression Patterns ·Naomi L. Baker, Kerry A. Miller, Donald F. Newgreen, Peter G. Farlie	7
6	A Mouse Splice-Site Mutant and Individuals with Atypical Chromosome 22q11.2 Deletions Demonstrate the Crucial Role for Crkl in Craniofacial and Pharyngeal Development 2014 ·Molecular Syndromology ·Kerry A. Miller, Tiong Yang Tan, (unknown), Susan M. White, Zornitza Stark, Ravi Savarirayan, Trent Burgess, Andrew A. Heggie, Georgina Caruana, John F. Bertram, John F. Bateman, Peter G. Farlie	8
7	Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction 2013 ·Hearing Research ·Louise H. Williams, Kerry A. Miller, Hans‐Henrik M. Dahl, Shehnaaz S.M. Manji	15
8	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
9	Eeyore: A Novel Mouse Model of Hereditary Deafness 2013 ·PLoS ONE ·Kerry A. Miller, Louise H. Williams, Hans‐Henrik M. Dahl, Shehnaaz S.M. Manji	1
10	bfb, a Novel ENU-Induced blebs Mutant Resulting from a Missense Mutation in Fras1 2013 ·PLoS ONE ·Kerry A. Miller, Christopher T. Gordon, (unknown), Georgina Caruana, John F. Bertram, John F. Bateman, Peter G. Farlie	7
11	Genome-Wide ENU Mutagenesis in Combination with High Density SNP Analysis and Exome Sequencing Provides Rapid Identification of Novel Mouse Models of Developmental Disease 2013 ·PLoS ONE ·Georgina Caruana, Peter G. Farlie, Adam H. Hart, Stefan Bagheri‐Fam, Megan J. Wallace, Michael S. Dobbie, Christopher T. Gordon, Kerry A. Miller, Belinda Whittle, Helen E. Abud, Ruth M. Arkell, Timothy J. Cole, Vincent R. Harley, Ian Smyth, John F. Bertram	14
12	Identification of Three Novel Hearing Loss Mouse Strains with Mutations in the Tmc1 Gene 2012 ·American Journal Of Pathology ·Shehnaaz S.M. Manji, Kerry A. Miller, Louise H. Williams, Hans‐Henrik M. Dahl	30
13	Inner Ear Morphology Is Perturbed in Two Novel Mouse Models of Recessive Deafness 2012 ·PLoS ONE ·Kerry A. Miller, Louise H. Williams, Elizabeth Rose, Michael J. Kuiper, Hans‐Henrik M. Dahl, Shehnaaz S.M. Manji	9
14	A Mutation in Synaptojanin 2 Causes Progressive Hearing Loss in the ENU-Mutagenised Mouse Strain Mozart 2011 ·PLoS ONE ·Shehnaaz S.M. Manji, Louise H. Williams, Kerry A. Miller, Lisa M. Ooms, Melanie Bahlo, Christina A. Mitchell, Hans‐Henrik M. Dahl	36
15	An ENU-Induced Mutation of Cdh23 Causes Congenital Hearing Loss, but No Vestibular Dysfunction, in Mice 2011 ·American Journal Of Pathology ·Shehnaaz S.M. Manji, Kerry A. Miller, Louise H. Williams, (unknown), (unknown), Elizabeth Rose, Melanie Bahlo, Michael J. Kuiper, Hans‐Henrik M. Dahl	23
16	Prediction and characterisation of a highly conserved, remote and cAMP responsive enhancer that regulates Msx1 gene expression in cardiac neural crest and outflow tract 2008 ·Developmental Biology ·Kerry A. Miller, Scott Davidson, (unknown), John Barrow, Marissa Lear, (unknown), Stefan Hoppler, Alasdair MacKenzie	15
17	A highly conserved Wnt-dependent TCF4 binding site within the proximal enhancer of the anti-myogenic Msx1 gene supports expression within Pax3-expressing limb bud muscle precursor cells 2007 ·Developmental Biology ·Kerry A. Miller, John Barrow, J. Martin Collinson, Scott Davidson, Marissa Lear, Robert E. Hill, Alasdair MacKenzie	31
18	Cellular co-expression of a LacZ marker gene driven by the amygdala-specific ECR1 enhancer with the substance P neuropeptide 2006 ·Molecular Psychiatry ·Scott Davidson, Kerry A. Miller, (unknown), (unknown), Alasdair MacKenzie	8
19	Is there a functional link between gene interdigitation and multi‐species conservation of synteny blocks? 2004 ·BioEssays ·Alasdair MacKenzie, Kerry A. Miller, J. Martin Collinson	24
20	Characterisation of a �-tubulin gene from the monogenean parasite, Gyrodactylus salaris Malmberg, 1957 2004 ·Parasitology Research ·Catherine Collins, Kerry A. Miller, Carey O. Cunningham	4

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