A.D. Roses

1.0k total citations
24 papers, 656 citations indexed

About

A.D. Roses is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, A.D. Roses has authored 24 papers receiving a total of 656 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in A.D. Roses's work include Genetic Neurodegenerative Diseases (6 papers), RNA and protein synthesis mechanisms (4 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). A.D. Roses is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), RNA and protein synthesis mechanisms (4 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). A.D. Roses collaborates with scholars based in United States, United Kingdom and Austria. A.D. Roses's co-authors include Jeffery M. Vance, E N Prystowsky, Edward L.C. Pritchett, John D. Gallagher, M. Ben Hamida, Felicia Lennon, Margaret A Pericak‐Vance, Christiane Ben Hamida, Kamel Ben Othmane and Larry H. Yamaoka and has published in prestigious journals such as Science, Nucleic Acids Research and Circulation.

In The Last Decade

A.D. Roses

24 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A.D. Roses United States 13 338 289 160 92 72 24 656
Tada-aki Hori Japan 8 440 1.3× 395 1.4× 304 1.9× 51 0.6× 86 1.2× 8 1.0k
Alessandro Malandrini Italy 16 448 1.3× 246 0.9× 134 0.8× 130 1.4× 71 1.0× 48 734
Usha R. Reddy United States 14 431 1.3× 349 1.2× 109 0.7× 45 0.5× 58 0.8× 22 702
G Haase France 9 245 0.7× 257 0.9× 175 1.1× 55 0.6× 86 1.2× 12 580
Sandra Gill United States 11 481 1.4× 461 1.6× 83 0.5× 117 1.3× 48 0.7× 15 880
Dong-Hui Chen United States 9 370 1.1× 277 1.0× 127 0.8× 39 0.4× 25 0.3× 10 579
Laura Davis Keppen United States 14 400 1.2× 419 1.4× 118 0.7× 182 2.0× 26 0.4× 23 887
A. Dautigny France 16 626 1.9× 209 0.7× 74 0.5× 117 1.3× 38 0.5× 31 1.0k
Silvia Rathke‐Hartlieb Germany 9 554 1.6× 325 1.1× 317 2.0× 137 1.5× 103 1.4× 9 979
Hjörvar Pétursson Iceland 3 285 0.8× 232 0.8× 338 2.1× 136 1.5× 66 0.9× 4 877

Countries citing papers authored by A.D. Roses

Since Specialization
Citations

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

Fields of papers citing papers by A.D. Roses

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A.D. Roses

This figure shows the co-authorship network connecting the top 25 collaborators of A.D. Roses. A scholar is included among the top collaborators of A.D. Roses 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 A.D. Roses. A.D. Roses is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hulette, Christine M., Jeffery M. Vance, A.D. Roses, et al.. (1999). Neuropathological Features of Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17q21–22 (FTDP-17). Journal of Neuropathology & Experimental Neurology. 58(8). 859–866. 42 indexed citations
2.
Deltas, Constantinos, et al.. (1996). Complete coding sequence, exon/intron arrangement and chromosome location of ZNF45, a KRAB-domain-containing gene. Cytogenetic and Genome Research. 75(4). 230–233. 9 indexed citations
3.
Small, Kent W., et al.. (1993). North Carolina macular dystrophy (MCDR1). Ophthalmic Paediatrics and Genetics. 14(4). 143–150. 37 indexed citations
4.
Mihovilovic, Mirta, Yosuke Mai, Michael H. Herbstreith, et al.. (1993). Splicing of an Anti-sense Alu Sequence Generates a Coding Sequence Variant for the α-3 Subunit of a Neuronal Acetylcholine Receptor. Biochemical and Biophysical Research Communications. 197(1). 137–144. 12 indexed citations
5.
Othmane, Kamel Ben, Felicia Lennon, Christiane Ben Hamida, et al.. (1993). Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Human Molecular Genetics. 2(10). 1625–1628. 136 indexed citations
6.
Kazantsev, A.D., Larry H. Yamaoka, & A.D. Roses. (1992). A dinucleotide repeat polymorphism in the human Na+,K+ATPase, alpha subunit (ATP1A3) gene. Nucleic Acids Research. 20(5). 1164–1164. 6 indexed citations
7.
Gilbert, James, et al.. (1992). The identification and characterization of KRAB-domain-containing zinc finger proteins. Genomics. 12(3). 581–589. 19 indexed citations
8.
Goodkin, Donald E., et al.. (1991). Diagnostic Criteria for Multiple Sclerosis Research Involving Multiply Affected Families. Archives of Neurology. 48(8). 805–807. 41 indexed citations
9.
Alberts, Mark J., Margaret A Pericak‐Vance, Gaetano Finocchiaro, et al.. (1991). Rsal RFLP for electron transport flavoprotein-beta(ETFB). Nucleic Acids Research. 19(14). 4021–4021. 2 indexed citations
10.
Samson, Françoise, et al.. (1990). Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA. Journal of Neuroscience Research. 27(4). 441–451. 12 indexed citations
11.
Oerlemans, Frank, H.J.M. Smeets, Jan Schepens, et al.. (1989). Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q. Genomics. 4(3). 384–396. 67 indexed citations
12.
Ciccone, Carla, et al.. (1989). A polymorphic DNA sequence (174-3.7) on chromosome 19 [D19S58]. Nucleic Acids Research. 17(23). 10144–10144. 1 indexed citations
13.
Siddique, Teepu, Margaret A. Pericak‐Vance, Benjamin Rix Brooks, et al.. (1989). Linkage analysis in familial amyotrophic lateral sclerosis. Neurology. 39(7). 919–919. 43 indexed citations
14.
Schmechel, D. E., Paul J. Marangos, Brian M. Martin, et al.. (1987). Localization of neuron-specific enolase (NSE) mRNA in human brain. Neuroscience Letters. 76(2). 233–238. 34 indexed citations
15.
Bartlett, Richard J., M. A. Pericak‐Vance, Larry H. Yamaoka, et al.. (1987). A New Probe for the Diagnosis of Myotonic Muscular Dystrophy. Science. 235(4796). 1648–1650. 56 indexed citations
16.
Greenberg, Steven J., et al.. (1984). Autologous mixed lymphocyte reaction in patients with myasthenia gravis: correlation with disease activity.. The Journal of Immunology. 132(3). 1229–1236. 12 indexed citations
17.
Prystowsky, E N, Edward L.C. Pritchett, A.D. Roses, & John D. Gallagher. (1979). The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic studies.. Circulation. 60(6). 1360–1364. 78 indexed citations
18.
Cabero, L., et al.. (1976). A comparative study between the values of lecithin, sphingomyelin, lysolecithin, the L/S Index, and the CLEMENTS test in amniotic fluid. Journal of Perinatal Medicine. 4(2). 111–117. 1 indexed citations
19.
Cabero, L., et al.. (1976). INFLUENCE OF LABOUR ON THE LECITHIN, LECITHIN/ SPHINGOMYELIN (L/S) RATIO AND PALMITIC ACID VALUES IN THE AMNIOTIC FLUID. BJOG An International Journal of Obstetrics & Gynaecology. 83(6). 452–453. 11 indexed citations
20.
Roses, A.D., et al.. (1975). Phenytoin and Membrane Fluidity in Myotonic Dystrophy. Archives of Neurology. 32(8). 535–538. 18 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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