R.J. Daniels

1.8k total citations
23 papers, 1.4k citations indexed

About

R.J. Daniels is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, R.J. Daniels has authored 23 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Genetics. Recurrent topics in R.J. Daniels's work include Neurogenetic and Muscular Disorders Research (13 papers), RNA modifications and cancer (13 papers) and RNA Research and Splicing (6 papers). R.J. Daniels is often cited by papers focused on Neurogenetic and Muscular Disorders Research (13 papers), RNA modifications and cancer (13 papers) and RNA Research and Splicing (6 papers). R.J. Daniels collaborates with scholars based in United Kingdom, United States and India. R.J. Daniels's co-authors include Victor Dubowitz, Kay E. Davies, Linda M. Brzustowicz, T. Conrad Gilliam, Jürg Ott, Thomas Lehner, Lucio H. Castilla, T. L. Munsat, Graciela K. Penchaszadeh and David Wood and has published in prestigious journals such as Nature, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

R.J. Daniels

22 papers receiving 1.3k citations

Peers

Countries citing papers authored by R.J. Daniels

Since Specialization

Citations

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

Fields of papers citing papers by R.J. Daniels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R.J. Daniels

This figure shows the co-authorship network connecting the top 25 collaborators of R.J. Daniels. A scholar is included among the top collaborators of R.J. Daniels 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 R.J. Daniels. R.J. Daniels 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	Role emerging placements: A success story in a climate of cutbacks 2007 ·R.J. Daniels, Helen Martin	1
2	Peptide signal molecules and bacteriocins in Gram-negative bacteria: a genome-wide in silico screening for peptides containing a double-glycine leader sequence and their cognate transporters 2004 ·Peptides ·Gunter Dirix, Pieter Monsieurs, Bruno Dombrecht, R.J. Daniels, Kathleen Marchal, Jozef Vanderleyden, Jan Michiels	95
3	The human GPI1 gene is required for efficient glycosylphosphatidylinositol biosynthesis 2001 ·Gene ·Andreas Tiede, R.J. Daniels, Douglas R. Higgs, (unknown), Reinhold Schmidt, Jörg Schubert	5
4	Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16 2001 ·Human Molecular Genetics ·R.J. Daniels	73
5	Localization, expression and genomic structure of the gene encoding the human serine protease testisin 2000 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·John D. Hooper, (unknown), (unknown), Lara M. Cullen, Raman Sood, R.J. Daniels, (unknown), (unknown), Douglas R. Higgs, Daniel L. Kastner, Steven M. Ogbourne, Martín F. Pera, Elizabeth C. Jazwinska, Toni Antalis	0
6	Maternal Mosaicism for a Second Mutational Event in a Type I Spinal Muscular Atrophy Family 1998 ·The American Journal of Human Genetics ·Louise J. Campbell, R.J. Daniels, Victor Dubowitz, Kay E. Davies	19
7	Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q 1995 ·Neuromuscular Disorders ·Victor Dubowitz, R.J. Daniels, Kay E. Davies	19
8	Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele. 1995 ·Journal of Medical Genetics ·R.J. Daniels, Louise J. Campbell, Nanda R. Rodrigues, Michael J. Francis, Karen Morrison, Michael D. McLean, Alex MacKenzie, Jaakko Ignatius, Victor Dubowitz, Kay E. Davies	14
9	An Investigation of Genetic Heterogeneity and Linkage Disequilibrium in 161 Families with Spinal Muscular Atrophy 1994 ·Genomics ·Chantal Mérette, Linda M. Brzustowicz, R.J. Daniels, Kay E. Davies, T. Conrad Gilliam, Judith Melki, Arnold Münnich, Margaret A. Pericak‐Vance, Teepu Siddique, (unknown), Brunhilde Wirth, J. Ott	8
10	Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13. 1994 ·PubMed ·Aspasia Theodosiou, Karen Morrison, (unknown), R.J. Daniels, Louise J. Campbell, Michael J. Francis, Zóe Christodoulou, Kay E. Davies	32
11	Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at D5S681 1993 ·Human Molecular Genetics ·Karen Morrison, R.J. Daniels, Louise J. Campbell, John D. McPherson, Kay E. Davies	7
12	Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA) 1993 ·Human Genetics ·Karen Morrison, R.J. Daniels, G K Suthers, Geraldine Flynn, Michael J. Francis, Prabhjit K. Grewal, C Dennis, Veronica J. Buckle, Jaakko Ignatius, Victor Dubowitz, K.E. Davies	9
13	A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13 1993 ·Human Molecular Genetics ·Michael J. Francis, Karen Morrison, Louise J. Campbell, Prabhjit K. Grewal, Zóe Christodoulou, R.J. Daniels, Anthony P. Monaco, (unknown), John D. McPherson, John J. Wasmuth, Kay E. Davies	63
14	Complete and partial XY sex reversal associated with terminal deletion of 10q: Report of 2 cases and literature review 1993 ·American Journal of Medical Genetics ·Andrew O.M. Wilkie, (unknown), Piers E.F. Daubeney, David Grant, R.J. Daniels, M. Mullarkey, Nabeel A. Affara, M Fitchett, Susan Huson	103
15	High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5. 1992 ·PubMed ·Karen Morrison, R.J. Daniels, G K Suthers, Geraldine Flynn, Michael J. Francis, Veronica J. Buckle, Kay E. Davies	30
16	Linkage analysis of spinal muscular atrophy 1992 ·Genomics ·R.J. Daniels, Neil H. Thomas, Ruth N. MacKinnon, Thomas Lehner, Jürg Ott, Tracey Flint, Victor Dubowitz, Jaakko Ignatius, M. Donner, Klaus Zerres, Marcella Rietschel, W. O. C. M. Cookson, Linda M. Brzustowicz, T. Conrad Gilliam, Kay E. Davies	28
17	Molecular studies of spinal muscular atrophy 1991 ·Neuromuscular Disorders ·Kay E. Davies, Neil H. Thomas, R.J. Daniels, Victor Dubowitz	4
18	Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3 1990 ·Nature ·Linda M. Brzustowicz, Thomas Lehner, Lucio H. Castilla, Graciela K. Penchaszadeh, Kirk C. Wilhelmsen, R.J. Daniels, K.E. Davies, M. Leppert, F. A. Ziter, David Wood, Victor Dubowitz, Klaus Zerres, I Hausmanowa-Pétrusewicz, Jürg Ott, T. L. Munsat, T. Conrad Gilliam	449
19	Genetic homogeneity between acute and chronic forms of spinal muscular atrophy 1990 ·Nature ·T. Conrad Gilliam, Linda M. Brzustowicz, Lucio H. Castilla, Thomas Lehner, Graciela K. Penchaszadeh, R.J. Daniels, Barbara C. Byth, James A. Knowles, Jenni Hislop, (unknown), Victor Dubowitz, T. L. Munsat, Jürg Ott, Kay E. Davies	257
20	Characterization of deletions in the dystrophin gene giving mild phenotypes 1990 ·American Journal of Medical Genetics ·Donald R. Love, Tracey Flint, (unknown), J.F. Bloomfield, R.J. Daniels, Susan M. Forrest, Orazio Gabrielli, (unknown), Giuseppe Novelli, Kay E. Davies	28

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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