Stuart G. Fischer

4.4k total citations · 2 hit papers
27 papers, 2.5k citations indexed

About

Stuart G. Fischer is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Stuart G. Fischer has authored 27 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Surgery. Recurrent topics in Stuart G. Fischer's work include Diabetes and associated disorders (4 papers), DNA and Nucleic Acid Chemistry (4 papers) and Microfluidic and Capillary Electrophoresis Applications (3 papers). Stuart G. Fischer is often cited by papers focused on Diabetes and associated disorders (4 papers), DNA and Nucleic Acid Chemistry (4 papers) and Microfluidic and Capillary Electrophoresis Applications (3 papers). Stuart G. Fischer collaborates with scholars based in United States, Italy and United Kingdom. Stuart G. Fischer's co-authors include Leonard S. Lerman, R Myers, Tom Maniatis, Eftìhia Cayanis, Sergey Kalachikov, James A. Knowles, Jane H. Morse, Robyn J. Barst, Susan L. Slager and Zemin Deng and has published in prestigious journals such as Cell, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Stuart G. Fischer

27 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

2000 861 citations Zemin Deng, Jane H. Morse et al. The American Journal of Human Genetics profile →
Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis

1985 460 citations Stuart G. Fischer et al. profile →

Peers

Stuart G. Fischer

PRM

CCM

GENET

Yoichi Sakata Japan

Kate Montgomery United States

Zongbin Cui China

Takamichi Nakamura Japan

Pudur Jagadeeswaran United States

Joanna L. James New Zealand

Michael G. Tomlinson United Kingdom

Gerolamo Lanfranchi Italy

Ramón Muñoz‐Chápuli Spain

Steven C. Greenway Canada

Yoichi Sakata Japan

Stuart G. Fischer

2.0k ×1.8

1.0k ×1.2

PRM

462 ×1.4

CCM

549 ×1.8

GENET

463 ×1.6

GENET

Citations per year, relative to Stuart G. Fischer Stuart G. Fischer (= 1×) peers Yoichi Sakata

Countries citing papers authored by Stuart G. Fischer

Since Specialization

Citations

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

Fields of papers citing papers by Stuart G. Fischer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stuart G. Fischer. 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 Stuart G. Fischer. The network helps show where Stuart G. Fischer may publish in the future.

Co-authorship network of co-authors of Stuart G. Fischer

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Watanabe, Kazuhisa, Richard Rausch, Dieter Egli, et al.. (2018). ILDR2 has a negligible role in hepatic steatosis. PLoS ONE. 13(5). e0197548–e0197548. 2 indexed citations

Watanabe, Kazuhisa, Kazuhiro Nakayama, Satoshi Ohta, et al.. (2016). ZNF70, a novel ILDR2-interacting protein, contributes to the regulation of HES1 gene expression. Biochemical and Biophysical Research Communications. 477(4). 712–716. 12 indexed citations

Watanabe, Kazuhisa, Elizabeth Watson, María Laura Cremona, et al.. (2013). ILDR2: An Endoplasmic Reticulum Resident Molecule Mediating Hepatic Lipid Homeostasis. PLoS ONE. 8(6). e67234–e67234. 30 indexed citations

Chung, Wendy K., Thomas C. Jaramillo, Rudolph L. Leibel, et al.. (2008). Absence epilepsy in apathetic, a spontaneous mutant mouse lacking the h channel subunit, HCN2. Neurobiology of Disease. 33(3). 499–508. 61 indexed citations

Chung, Wendy K., Jean-Claude Chèvre, Elizabeth Watson, et al.. (2008). Positional Cloning of “Lisch-like”, a Candidate Modifier of Susceptibility to Type 2 Diabetes in Mice. PLoS Genetics. 4(7). e1000137–e1000137. 49 indexed citations

Deng, Zemin, Jane H. Morse, Susan L. Slager, et al.. (2000). Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene. The American Journal of Human Genetics. 67(3). 737–744. 861 indexed citations breakdown →

Zhang, Peisen, et al.. (1999). Integrated Mapping Package—A Physical Mapping Software Tool Kit. Genomics. 55(1). 78–87. 5 indexed citations

Valhmu, Wilmot B., Glyn D. Palmer, Jennifer Dobson, Stuart G. Fischer, & Anthony Ratcliffe. (1998). Regulatory Activities of the 5′- and 3′-Untranslated Regions and Promoter of the Human Aggrecan Gene. Journal of Biological Chemistry. 273(11). 6196–6202. 20 indexed citations

Cayanis, Eftìhia, James J. Russo, Ivana Šunjevarić, et al.. (1998). High-Resolution YAC–Cosmid–STS Map of Human Chromosome 13. Genomics. 47(1). 26–43. 21 indexed citations

10.

Valhmu, Wilmot B., Nathaniel M. Bachrach, Fatemeh Saed‐Nejad, et al.. (1998). Load-Controlled Compression of Articular Cartilage Induces a Transient Stimulation of Aggrecan Gene Expression. Archives of Biochemistry and Biophysics. 353(1). 29–36. 116 indexed citations

11.

Venkatraj, V.S., et al.. (1997). Genomic Cloning and Chromosomal Assignment of the E2F Dimerization PartnerTFDPGene Family. Genomics. 39(1). 95–98. 19 indexed citations

12.

Ratcliffe, Anthony, Stuart G. Fischer, Wilmot B. Valhmu, et al.. (1996). MOLECULAR MECHANISMS USED IN THE REGULATION OF AGGRECAN AND LINK PROTEIN SYNTHESIS BY CHONDROCYTES. American Journal of Therapeutics. 3(2). 129–133. 1 indexed citations

13.

Fischer, Stuart G., Eftìhia Cayanis, James J. Russo, et al.. (1994). Assembly of Ordered Contigs of Cosmids Selected with YACs of Human Chromosome 13. Genomics. 21(3). 525–537. 12 indexed citations

14.

Warburton, Dorothy, Umadevi Tantravahi, Carolyn Lee, et al.. (1993). Regional Localization of 32 NotI-HindIII Fragments from a Human Chromosome 13 Library by a Somatic Cell Hybrid Panel and in Situ Hybridization. Genomics. 16(2). 355–360. 6 indexed citations

15.

Petrukhin, Konstantin, Marcy C. Speer, Eftìhia Cayanis, et al.. (1993). A Microsatellite Genetic Linkage Map of Human Chromosome 13. Genomics. 15(1). 76–85. 45 indexed citations

16.

Grimm, Nancy B., H. Maurice Valett, Emily H. Stanley, & Stuart G. Fischer. (1991). Contribution of the hyporheic zone to stability of an arid-land stream. SIL Proceedings 1922-2010. 24(3). 1595–1599. 37 indexed citations

17.

Dabestani, Ali, Katsu Takenaka, Byron J. Allen, et al.. (1988). Effects of spontaneous respiration on diastolic left ventricular filling assessed by pulsed Doppler echocardiography. The American Journal of Cardiology. 61(15). 1356–1358. 36 indexed citations

18.

Jones, Frederick S., et al.. (1985). Detection of sickle-cell mutation by electrophoresis of partial RNA:DNA hybrids following solution hybridization. Gene. 39(1). 77–83. 4 indexed citations

19.

Fischer, Stuart G.. (1983). [29]Peptide mapping in gels. Methods in enzymology on CD-ROM/Methods in enzymology. 100. 424–430. 22 indexed citations

20.

Cole, Jonathan J. & Stuart G. Fischer. (1979). Nutrient budgets of a temporary pond ecosystem. Hydrobiologia. 63(3). 213–222. 20 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.

Explore authors with similar magnitude of impact