Howard R. Slater

5.1k total citations
99 papers, 3.0k citations indexed

About

Howard R. Slater is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Howard R. Slater has authored 99 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Genetics, 40 papers in Molecular Biology and 26 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Howard R. Slater's work include Genomic variations and chromosomal abnormalities (53 papers), Genetics and Neurodevelopmental Disorders (34 papers) and Prenatal Screening and Diagnostics (25 papers). Howard R. Slater is often cited by papers focused on Genomic variations and chromosomal abnormalities (53 papers), Genetics and Neurodevelopmental Disorders (34 papers) and Prenatal Screening and Diagnostics (25 papers). Howard R. Slater collaborates with scholars based in Australia, United States and United Kingdom. Howard R. Slater's co-authors include Lucille Voullaire, L. Wilton, R. Williamson, K. H. Andy Choo, Trent Burgess, David J. Amor, J. Shepherd, C.J. Packard, Damien L. Bruno and David Francis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Howard R. Slater

98 papers receiving 2.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Howard R. Slater Australia	32	1.8k	1.3k	795	490	452	99	3.0k
Bassem A. Bejjani United States	36	2.6k 1.5×	1.8k 1.3×	1.0k 1.3×	577 1.2×	157 0.3×	83	4.1k
Leda Dalprà Italy	32	1.2k 0.7×	1.5k 1.1×	490 0.6×	253 0.5×	206 0.5×	119	3.3k
Mary C. Phelan United States	25	1.4k 0.8×	1.0k 0.8×	415 0.5×	284 0.6×	480 1.1×	68	2.4k
Antonio Novelli Italy	27	1.7k 1.0×	1.5k 1.2×	423 0.5×	213 0.4×	158 0.3×	305	3.4k
Marwan Shinawi United States	32	1.5k 0.8×	2.4k 1.8×	375 0.5×	146 0.3×	218 0.5×	137	4.3k
Nicole de Leeuw Netherlands	30	2.4k 1.4×	1.4k 1.1×	744 0.9×	456 0.9×	148 0.3×	104	3.2k
Bruce Bennetts Australia	31	1.4k 0.8×	1.3k 1.0×	246 0.3×	134 0.3×	315 0.7×	101	3.2k
M Prieur France	26	1.5k 0.9×	1.4k 1.1×	449 0.6×	445 0.9×	184 0.4×	75	2.6k
J. F. Mattéi France	29	1.7k 1.0×	1.5k 1.2×	530 0.7×	417 0.9×	125 0.3×	87	2.9k
Swaroop Aradhya United States	26	1.9k 1.1×	1.2k 0.9×	590 0.7×	145 0.3×	130 0.3×	85	2.8k

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

Jacobson, Angela, Amal Abu Rayyan, Süleyman Gülsüner, et al.. (2025). Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms. Journal of Medical Genetics. 62(10). 617–623.

Field, Michael, Tracy Dudding‐Byth, Marta Arpone, et al.. (2019). Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing. International Journal of Molecular Sciences. 20(16). 3907–3907. 13 indexed citations

Greitzer, E. M., et al.. (2018). AIAA\/IEEE Electric Aircraft Technologies Symposium. IEEE Electrification Magazine. 6(2). 107–107. 1 indexed citations

Dudding, Tracy, Marta Arpone, David Francis, et al.. (2016). Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes. 7(9). 68–68. 6 indexed citations

Arpone, Marta, David Francis, Xin Li, et al.. (2016). Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report. American Journal of Medical Genetics Part A. 170(12). 3327–3332. 20 indexed citations

Cotter, Megan, Alison D. Archibald, Belinda McClaren, et al.. (2016). Clinical audit of genetic testing and referral patterns for fragile X and associated conditions. American Journal of Medical Genetics Part A. 170(6). 1439–1449. 7 indexed citations

Slater, Howard R., David Francis, Desirée du Sart, et al.. (2015). Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt Analysis. Clinical Chemistry. 62(2). 343–352. 25 indexed citations

Cornish, Kim, Claudine M. Kraan, Minh Bui, et al.. (2015). Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women. Neurology. 84(16). 1631–1638. 26 indexed citations

Loesch, Danuta Z., Minh Bui, Andrea Schneider, et al.. (2014). Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion. Clinical Genetics. 87(2). 173–178. 35 indexed citations

10.

Godler, David E., Y. Inaba, Cindy Skinner, et al.. (2013). 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. Human Molecular Genetics. 22(8). 1516–1524. 19 indexed citations

11.

Martyn, Melissa, Vicki Anderson, Alison D. Archibald, et al.. (2013). 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. BMJ Open. 3(9). e003660–e003660. 12 indexed citations

12.

Godler, David E., Howard R. Slater, Minh Bui, et al.. (2012). Fragile X Mental Retardation 1 (FMR1) Intron 1 Methylation in Blood Predicts Verbal Cognitive Impairment in Female Carriers of Expanded FMR1 Alleles: Evidence from a Pilot Study. Clinical Chemistry. 58(3). 590–598. 31 indexed citations

13.

Herlihy, Amy S., Charles E. Schwartz, Cindy Skinner, et al.. (2012). 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. Genetics in Medicine. 15(4). 290–298. 18 indexed citations

14.

Godler, David E., Howard R. Slater, Minh Bui, et al.. (2011). FMR1 Intron 1 Methylation Predicts FMRP Expression in Blood of Female Carriers of Expanded FMR1 Alleles. Journal of Molecular Diagnostics. 13(5). 528–536. 37 indexed citations

15.

Loesch, Danuta Z., David E. Godler, Andrew Evans, et al.. (2011). 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. Genetics in Medicine. 13(5). 392–399. 65 indexed citations

16.

Godler, David E., Flora Tassone, Danuta Z. Loesch, et al.. (2010). Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio. Human Molecular Genetics. 19(8). 1618–1632. 85 indexed citations

17.

Loesch, Danuta Z., David E. Godler, Mahmoud Shekari Khaniani, et al.. (2009). Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: Preliminary data suggest an involvement of epigenetic mechanisms. American Journal of Medical Genetics Part A. 149A(10). 2306–2310. 22 indexed citations

18.

Metcalfe, Sylvia A., Alison D. Archibald, Trent Burgess, et al.. (2008). A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study. Genetics in Medicine. 10(7). 525–535. 45 indexed citations

19.

Amor, David J., et al.. (2004). Human centromere repositioning “in progress”. Proceedings of the National Academy of Sciences. 101(17). 6542–6547. 192 indexed citations

20.

Apostolopoulos, Jim, Rosemary L. Sparrow, Janet McLeod, et al.. (2001). Identification and Characterization of a Novel Family of Mammalian Ependymin-Related Proteins (MERPs) in Hematopoietic, Nonhematopoietic, and Malignant Tissues. DNA and Cell Biology. 20(10). 625–635. 37 indexed citations

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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