Robert A. Conte

522 total citations
41 papers, 361 citations indexed

About

Robert A. Conte is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Robert A. Conte has authored 41 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 26 papers in Plant Science and 21 papers in Molecular Biology. Recurrent topics in Robert A. Conte's work include Chromosomal and Genetic Variations (26 papers), Genomic variations and chromosomal abnormalities (24 papers) and Genomics and Chromatin Dynamics (14 papers). Robert A. Conte is often cited by papers focused on Chromosomal and Genetic Variations (26 papers), Genomic variations and chromosomal abnormalities (24 papers) and Genomics and Chromatin Dynamics (14 papers). Robert A. Conte collaborates with scholars based in United States, Philippines and Qatar. Robert A. Conte's co-authors include Ram S. Verma, Michael J. Macera, C.J. Godec, Rhea U. Vallente, K.H. Ramesh, T J Mathews, Martin G. Bialer, D. Kanjilal, Swarna Gogineni and Rama Shanker Verma and has published in prestigious journals such as American Journal of Physical Anthropology, Journal of Medical Genetics and Heredity.

In The Last Decade

Robert A. Conte

39 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert A. Conte United States 11 257 167 163 89 34 41 361
J L Watt United Kingdom 13 298 1.2× 191 1.1× 130 0.8× 161 1.8× 20 0.6× 19 462
Satoshi Ishikiriyama Japan 10 283 1.1× 289 1.7× 52 0.3× 128 1.4× 13 0.4× 21 472
Roberta Santos Guilherme Brazil 14 426 1.7× 213 1.3× 194 1.2× 146 1.6× 11 0.3× 26 512
Ron Hochstenbach Netherlands 11 340 1.3× 306 1.8× 162 1.0× 87 1.0× 11 0.3× 18 512
B. Redeker Netherlands 7 238 0.9× 316 1.9× 38 0.2× 101 1.1× 30 0.9× 11 397
Peter Papenhausen United States 9 194 0.8× 154 0.9× 105 0.6× 49 0.6× 8 0.2× 15 341
T. M. Schroeder-Kurth Germany 7 143 0.6× 227 1.4× 135 0.8× 47 0.5× 15 0.4× 10 330
E. Zackai United States 5 179 0.7× 146 0.9× 65 0.4× 60 0.7× 8 0.2× 7 243
C. Mignon France 11 176 0.7× 327 2.0× 46 0.3× 74 0.8× 31 0.9× 14 434
Angelo Selicorni Italy 10 474 1.8× 322 1.9× 221 1.4× 161 1.8× 12 0.4× 14 584

Countries citing papers authored by Robert A. Conte

Since Specialization
Citations

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

Fields of papers citing papers by Robert A. Conte

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert A. Conte

This figure shows the co-authorship network connecting the top 25 collaborators of Robert A. Conte. A scholar is included among the top collaborators of Robert A. Conte 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 Robert A. Conte. Robert A. Conte 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.
Conte, Robert A., Rhea U. Vallente, & Ram S. Verma. (1999). Localization of subtelomeric sequences of human chromosomes 1q, 11p, 13q, and 16q in the higher primates. Genetica. 105(1). 31–34. 3 indexed citations
2.
Verma, Ram S., et al.. (1999). Chromosomal Basis of Adenocarcinoma of the Prostate. Cancer Investigation. 17(6). 441–447. 57 indexed citations
3.
Conte, Robert A., Rhea U. Vallente, & Ram S. Verma. (1998). Evolutionary divergence of the oncogenes GLI, HST and INT2. Heredity. 81(1). 10–13. 1 indexed citations
4.
Vallente, Rhea U., et al.. (1998). Molecular phylogenetics of the hominoid Y chromosome. Journal of Human Genetics. 43(3). 185–186. 2 indexed citations
5.
Tarzami, Sima T., et al.. (1997). Unique genomic sequences in human chromosome 16p are conserved in the great apes. Molecular and General Genetics MGG. 253(4). 512–514. 1 indexed citations
6.
Vallente, Rhea U., Robert A. Conte, & Ram S. Verma. (1997). Brief communication: Comparative mapping of the human estrogen receptor (ESR) and the Kallmann (KAL) regions to the chromosomes of the great apes. American Journal of Physical Anthropology. 103(4). 561–563. 2 indexed citations
7.
Conte, Robert A., et al.. (1997). Delineation of a ring chromosome 16 by the FISH‐technique: a case report with review. Clinical Genetics. 51(3). 196–199. 21 indexed citations
8.
Verma, Ram S., et al.. (1997). An unusual G-negative band within 1qh region a rare variant or an abnormality?. PubMed. 40(4). 229–31.
9.
Conte, Robert A., et al.. (1997). Paracentric inversion involving the long arm of chromosome 9 resulting in deletion of abl gene. American Journal of Medical Genetics. 68(4). 409–411. 4 indexed citations
10.
Vallente, Rhea U., Robert A. Conte, K.H. Ramesh, & Ram S. Verma. (1996). Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9. Human Genetics. 98(5). 576–580. 26 indexed citations
11.
Conte, Robert A., et al.. (1996). Molecular characterization of 21p‐variant chromosome. Clinical Genetics. 50(2). 103–105. 3 indexed citations
12.
Verma, Ram S., K.H. Ramesh, Rhea U. Vallente, & Robert A. Conte. (1996). Mapping the homolog of the human Rb1 gene to Chromosome 14 of higher primates. Mammalian Genome. 7(8). 591–592. 3 indexed citations
13.
Tarzami, Sima T., et al.. (1996). A unique genomic sequence in the Wolf-Hirschhorn syndrome [WHS] region of humans is conserved in the great apes. Genetica. 98(2). 217–219. 1 indexed citations
14.
Verma, Ram S., et al.. (1994). Fish technique What's all the fuss about?. Genetic Analysis Biomolecular Engineering. 11(4). 106–109. 2 indexed citations
15.
Conte, Robert A. & Ram S. Verma. (1994). Counterstained enhancement of TaqI resistant sites after distamycin A/diamidinophenylindole treatment. Histochemistry and Cell Biology. 102(6). 433–435. 1 indexed citations
16.
Mathews, T J, et al.. (1993). Chromosomal Anomalies in 1,000 Children Referred with Suspected Genetic Disorders. Human Heredity. 43(3). 137–140. 11 indexed citations
17.
Verma, Ram S., et al.. (1992). Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16. Genetic Analysis Biomolecular Engineering. 9(5-6). 140–142. 1 indexed citations
18.
Verma, Ram S., et al.. (1992). The interstitial deletion of bands q33–35 of long arm of chromosome 7: a review with a new case report. Clinical Genetics. 41(2). 82–86. 16 indexed citations
19.
Conte, Robert A., et al.. (1992). Molecular characterization of ?inverted? pericentromeric heterochromatin of chromosome 3. Histochemistry and Cell Biology. 97(6). 509–510. 2 indexed citations
20.
Verma, Rama Shanker, et al.. (1991). A so-called rare heteromorphism of the human genome. Cytogenetic and Genome Research. 56(1). 63–63. 7 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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