Patrick D. Storto

933 total citations
21 papers, 735 citations indexed

About

Patrick D. Storto is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Patrick D. Storto has authored 21 papers receiving a total of 735 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in Patrick D. Storto's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Patrick D. Storto is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Patrick D. Storto collaborates with scholars based in United States. Patrick D. Storto's co-authors include Robert C. King, Susanne M. Gollin, Mukta M. Webber, Hynda K. Kleinman, Salmaan Quader, Ronald B. Herberman, Yukihiro Shimizu, Shunzaburo Iwatsuki, Jan F. Silverman and A J Demetris and has published in prestigious journals such as The American Journal of Human Genetics, International Journal of Cancer and BioEssays.

In The Last Decade

Patrick D. Storto

21 papers receiving 717 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Patrick D. Storto 381 250 119 96 94 21 735
Pierre Hutter 493 1.3× 352 1.4× 113 0.9× 74 0.8× 314 3.3× 48 1.2k
Max Kauer 324 0.9× 407 1.6× 102 0.9× 25 0.3× 78 0.8× 14 869
Klaus Brasch 895 2.3× 313 1.3× 39 0.3× 79 0.8× 170 1.8× 37 1.4k
Alain Zider 711 1.9× 181 0.7× 43 0.4× 31 0.3× 66 0.7× 27 1.1k
A.M. Dutrillaux 252 0.7× 162 0.6× 117 1.0× 35 0.4× 47 0.5× 29 527
P Meltzer 530 1.4× 218 0.9× 124 1.0× 16 0.2× 73 0.8× 5 930
Cristina Frías-López 335 0.9× 125 0.5× 28 0.2× 22 0.2× 97 1.0× 21 572
Paula K. Elder 686 1.8× 160 0.6× 30 0.3× 32 0.3× 101 1.1× 19 894
Leonie M. Quinn 1.4k 3.8× 177 0.7× 50 0.4× 32 0.3× 115 1.2× 50 1.8k
Brian Park 338 0.9× 123 0.5× 73 0.6× 125 1.3× 50 0.5× 14 604

Countries citing papers authored by Patrick D. Storto

Since Specialization
Citations

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

Fields of papers citing papers by Patrick D. Storto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick D. Storto

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick D. Storto. A scholar is included among the top collaborators of Patrick D. Storto 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 Patrick D. Storto. Patrick D. Storto 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.
Krishnamurti, Uma, Jennifer Hammers, Folefac Atem, Patrick D. Storto, & Jan F. Silverman. (2009). Poor prognostic significance of unamplified chromosome 17 polysomy in invasive breast carcinoma. Modern Pathology. 22(8). 1044–1048. 41 indexed citations
2.
Webber, Mukta M., et al.. (2001). Human cell lines as an in vitro/in vivo model for prostate carcinogenesis and progression. The Prostate. 47(1). 1–13. 4 indexed citations
3.
Webber, Mukta M., et al.. (2001). Human cell lines as an in vitro/in vivo model for prostate carcinogenesis and progression. The Prostate. 47(1). 1–13. 80 indexed citations
4.
O’Malley, Daniel P. & Patrick D. Storto. (1999). Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations. Prenatal Diagnosis. 19(2). 183–184. 11 indexed citations
5.
O’Malley, Daniel P. & Patrick D. Storto. (1999). Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations. Prenatal Diagnosis. 19(2). 183–184. 2 indexed citations
6.
Leichtman, Lawrence G., Joleen L. Zackowski, Patrick D. Storto, & Anna Newlin. (1996). Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: Case report and comparison with trisomy 9p. American Journal of Medical Genetics. 63(3). 434–437. 16 indexed citations
7.
Storto, Patrick D.. (1995). The Insect Ovary: Ultrastructure, previtellogenic growth and evolution. Invertebrate Reproduction & Development. 28(3). 217–218. 149 indexed citations
8.
O’Malley, Daniel P., et al.. (1994). Near-haploidy: Cytogenetic guidelines for the detection of an under-reported sub-group of acute lymphoblastic leukemia. The American Journal of Human Genetics. 55. 1 indexed citations
9.
Malone, Patrick S., et al.. (1993). Clonal chromosomal aberrations in a leiomyosarcoma of the sinonasal tract. Cancer Genetics and Cytogenetics. 65(1). 21–26. 8 indexed citations
10.
Brothman, Arthur R., et al.. (1992). Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male. Clinical Genetics. 42(1). 47–49. 8 indexed citations
11.
Gollin, Susanne M., Patrick D. Storto, Patrick S. Malone, et al.. (1992). Cytogenetic abnormalities in an ossifying fibroma from a patient with bilateral retinoblastoma. Genes Chromosomes and Cancer. 4(2). 146–152. 20 indexed citations
12.
Shimizu, Yukihiro, A J Demetris, Susanne M. Gollin, et al.. (1992). Two new human cholangiocarcinoma cell lines and their cytogenetics and responses to growth factors, hormones, cytokines or immunologic effector cells. International Journal of Cancer. 52(2). 252–260. 82 indexed citations
13.
Brothman, Arthur R., Peter B. Jacky, Linda A. Cannizzaro, et al.. (1992). Abstracts of presentations at the Thirtieth Annual American Cytogenetics Conference. Cytogenetic and Genome Research. 60(3-4). 257–269. 1 indexed citations
14.
Storto, Patrick D., Susan L. Saidman, Anthony J. Demetris, et al.. (1990). Chromosomal breakpoints in cholangiocarcinoma cell lines. Genes Chromosomes and Cancer. 2(4). 300–310. 49 indexed citations
15.
Storto, Patrick D. & Robert C. King. (1989). The role of polyfusomes in generating branched chains of cystocytes during Drosophila oogenesis. Developmental Genetics. 10(2). 70–86. 74 indexed citations
16.
Storto, Patrick D. & Robert C. King. (1988). Multiplicity of functions for the otu gene products during Drosophila oogenesis. Developmental Genetics. 9(2). 91–120. 49 indexed citations
17.
King, Robert C. & Patrick D. Storto. (1988). The role of the otu Gene in Drosophila oogenesis. BioEssays. 8(1). 18–24. 56 indexed citations
18.
Storto, Patrick D. & Robert C. King. (1987). Fertile heteroallelic combinations of mutant alleles of the otu locus of Drosophila melanogaster. Development Genes and Evolution. 196(4). 210–221. 23 indexed citations
19.
King, Robert C., et al.. (1986). Complementation between alleles at the ovarian tumor locus of Drosophila melanogaster. Developmental Genetics. 7(1). 1–20. 47 indexed citations
20.
King, Robert C., et al.. (1985). Cytophotometric evidence for the transformation of oocytes into nurse cells inDrosophila melanogaster. Histochemistry and Cell Biology. 82(2). 131–134. 8 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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