Howard R. Slater

5.1k citations

99 papers · 3.0k indexed · h-index 32

Genetics top 1%
Molecular Biology top 5%
Pediatrics, Perinatology and Child Health top 1%
Plant Science top 5%
Cognitive Neuroscience top 5%

Co-authors: Lucille Voullaire L. Wilton R. Williamson K. H. Andy Choo David J. Amor Trent Burgess J. Shepherd C.J. Packard
Topics: Genomic variations and chromosomal abnormalities (53 papers)Genetics and Neurodevelopmental Disorders (34 papers)Prenatal Screening and Diagnostics (25 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Transplantation
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry PLoS ONE
Partner nations: Australia United States United Kingdom

In The Last Decade

Howard R. Slater

98 papers receiving 2.9k citations

Peers

Countries citing papers authored by Howard R. Slater

Since Specialization

Citations

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

Fields of papers citing papers by Howard R. Slater

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Howard R. Slater. 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 Howard R. Slater. The network helps show where Howard R. Slater may publish in the future.

Co-authorship network of co-authors of Howard R. Slater

This figure shows the co-authorship network connecting the top 25 collaborators of Howard R. Slater. A scholar is included among the top collaborators of Howard R. Slater 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 Howard R. Slater. Howard R. Slater 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	Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms 2025 ·Journal of Medical Genetics ·Angela Jacobson,Amal Abu Rayyan,Süleyman Gülsüner,Howard R. Slater,(unknown),(unknown),(unknown),Jessica B. Mandell,(unknown),Eric Q. Konnick,Colin C. Pritchard,Mary‐Claire King,Tom Walsh,Brian H. Shirts	0
2	AIAA\/IEEE Electric Aircraft Technologies Symposium 2018 ·IEEE Electrification Magazine ·(unknown),(unknown),E. M. Greitzer,Howard R. Slater,(unknown),(unknown),Marija Ilić,(unknown),(unknown)	1
3	Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia 2016 ·Genes ·(unknown),Tracy Dudding,(unknown),Marta Arpone,David Francis,Xin Li,Howard R. Slater,Carolyn Rogers,Lesley Bretherton,Desirée du Sart,Robert Heard,David E. Godler	6
4	Clinical audit of genetic testing and referral patterns for fragile X and associated conditions 2016 ·American Journal of Medical Genetics Part A ·Megan Cotter,Alison D. Archibald,Belinda McClaren,Trent Burgess,David Francis,(unknown),Melissa Martyn,(unknown),Howard R. Slater,Jonathan Cohen,Sylvia A. Metcalfe	7
5	Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report 2016 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Marta Arpone,David Francis,Xin Li,Belinda Chong,Howard R. Slater,Carolyn Rogers,Lesley Bretherton,Matthew F. Hunter,Robert Heard,David E. Godler	20
6	Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt Analysis 2015 ·Clinical Chemistry ·(unknown),Howard R. Slater,David Francis,Desirée du Sart,Xin Li,David J. Amor,(unknown),Lorena Santa María,Víctor Faúndes,(unknown),César Trigo,(unknown),(unknown),David E. Godler	25
7	Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion 2014 ·Clinical Genetics ·Danuta Z. Loesch,Minh Bui,(unknown),Andrea Schneider,Elsdon Storey,Paul Stimpson,Trent Burgess,David Francis,Howard R. Slater,Flora Tassone,Randi J. Hagerman,David Hessl	35
8	Investigating and Correcting Plasma DNA Sequencing Coverage Bias to Enhance Aneuploidy Discovery 2014 ·PLoS ONE ·Dineika Chandrananda,Natalie Thorne,Devika Ganesamoorthy,Damien L. Bruno,Yuval Benjamini,Terence P. Speed,Howard R. Slater,Melanie Bahlo	21
9	Offering fragile X syndrome carrier screening: a prospective mixed-methods observational study comparing carrier screening of pregnant and non-pregnant women in the general population 2013 ·BMJ Open ·Melissa Martyn,Vicki Anderson,Alison D. Archibald,Rob Carter,Jonathan Cohen,M. B. Delatycki,Susan Donath,Jon Emery,J. Halliday,Melissa Hill,L. J. Sheffield,Howard R. Slater,Flora Tassone,(unknown),(unknown)	12
10	Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty 2013 ·Human Molecular Genetics ·David E. Godler,Y. Inaba,(unknown),Cindy Skinner,Minh Bui,David Francis,David J. Amor,John L. Hopper,Danuta Z. Loesch,Randi J. Hagerman,Charles E. Schwartz,Howard R. Slater	19
11	Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism 2011 ·Genetics in Medicine ·Danuta Z. Loesch,David E. Godler,Andrew Evans,Minh Bui,(unknown),Katya Kotschet,Nicholas Trost,Elsdon Storey,(unknown),Glynda Kinsella,David Francis,David R. Thorburn,Alison Venn,Howard R. Slater,Malcolm Horne	65
12	Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: Preliminary data suggest an involvement of epigenetic mechanisms 2009 ·American Journal of Medical Genetics Part A ·Danuta Z. Loesch,David E. Godler,Mahmoud Shekari Khaniani,Emma Gould,(unknown),Cheryl Dissanayake,Trent Burgess,Flora Tassone,Richard Huggins,Howard R. Slater,(unknown)	22
13	4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment 2009 ·European Journal of Medical Genetics ·Alison Yeung,Damien L. Bruno,Ingrid E. Scheffer,(unknown),Trent Burgess,Howard R. Slater,David J. Amor	49
14	A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study 2008 ·Genetics in Medicine ·Sylvia A. Metcalfe,(unknown),Alison D. Archibald,Trent Burgess,Veronica Collins,Anna Henry,Kathleen McNamee,Leslie J. Sheffield,Howard R. Slater,Samantha Wake,Jonathan Cohen	45
15	BAC-based PCR fragment microarray: High-resolution detection of chromosomal deletion and duplication breakpoints 2005 ·Human Mutation ·Hua Ren,Wendy S. Francis,Amber Boys,Anderly C. Chüeh,Nicholas C. Wong,(unknown),Lee H. Wong,(unknown),Howard R. Slater,K.H. Andy Choo	18
16	Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data 2005 ·Brain and Development ·Danuta Z. Loesch,Minh Bui,Wendy Kelso,Richard Huggins,Howard R. Slater,Garry L. Warne,Paul Bergman,Christine Rodda,Robert J. Mitchell,Margot Prior	37
17	Human centromere repositioning “in progress” 2004 ·Proceedings of the National Academy of Sciences ·David J. Amor,(unknown),(unknown),Jo K. Perry,Lee H. Wong,Howard R. Slater,K. H. Andy Choo	192
18	Identification and Characterization of a Novel Family of Mammalian Ependymin-Related Proteins (MERPs) in Hematopoietic, Nonhematopoietic, and Malignant Tissues 2001 ·DNA and Cell Biology ·Jim Apostolopoulos,Rosemary L. Sparrow,Janet McLeod,Fiona Collier,Phillip K. Darcy,Howard R. Slater,(unknown),Claudia C. Gregorio-King,Mark A. Kirkland	37
19	Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization 2000 ·Human Genetics ·Lucille Voullaire,Howard R. Slater,R. Williamson,L. Wilton	260
20	High frequency of t(12;21) in childhood acute lymphoblastic leukemia detected by RT-PCR 1998 ·Pathology ·David J. Amor,Elizabeth M. Algar,Howard R. Slater,Peter J. Smith	23

About Howard R. Slater

Howard R. Slater is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 99 papers that have together received 3.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (53 papers), Genetics and Neurodevelopmental Disorders (34 papers) and Prenatal Screening and Diagnostics (25 papers). The work is most often cited by research in Genetics (1.8k citations), Pediatrics, Perinatology and Child Health (795 citations) and Transplantation (93 citations). Howard R. Slater has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Lucille Voullaire, L. Wilton, R. Williamson, K. H. Andy Choo, David J. Amor, Trent Burgess, J. Shepherd, C.J. Packard, Damien L. Bruno and David Francis. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

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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