Christopher Winter

5.0k total citations · 1 hit paper
38 papers, 3.0k citations indexed

About

Christopher Winter is a scholar working on Molecular Biology, Epidemiology and Infectious Diseases. According to data from OpenAlex, Christopher Winter has authored 38 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Epidemiology and 6 papers in Infectious Diseases. Recurrent topics in Christopher Winter's work include Tuberculosis Research and Epidemiology (6 papers), Infectious Diseases and Tuberculosis (5 papers) and Developmental Biology and Gene Regulation (5 papers). Christopher Winter is often cited by papers focused on Tuberculosis Research and Epidemiology (6 papers), Infectious Diseases and Tuberculosis (5 papers) and Developmental Biology and Gene Regulation (5 papers). Christopher Winter collaborates with scholars based in United States, Canada and Switzerland. Christopher Winter's co-authors include Liqun Luo, Xudong Dai, Nilay S. Sethi, Yibin Kang, Bruce Wang, Jeffrey D. Axelrod, Anne Royou, Roger E. Karess, Jennifer O’Neil and Peter R. Strack and has published in prestigious journals such as Cell, Neuron and The Journal of Experimental Medicine.

In The Last Decade

Christopher Winter

34 papers receiving 3.0k citations

Hit Papers

FBW7 mutations in leukemi... 2007 2026 2013 2019 2007 100 200 300 400 500

Author Peers

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

Author Last Decade Papers Cites
Christopher Winter 2.1k 632 588 382 374 38 3.0k
Ma. Xenia G. Ilagan 3.2k 1.5× 579 0.9× 477 0.8× 477 1.2× 311 0.8× 27 4.3k
Josée Hamelin 1.7k 0.8× 380 0.6× 898 1.5× 567 1.5× 578 1.5× 50 4.3k
Federica Piccioni 2.1k 1.0× 677 1.1× 608 1.0× 387 1.0× 208 0.6× 49 3.0k
Alain Eychène 2.2k 1.1× 798 1.3× 402 0.7× 333 0.9× 234 0.6× 55 3.0k
Serge Roche 3.1k 1.5× 1.0k 1.6× 839 1.4× 371 1.0× 348 0.9× 92 4.5k
Julie L. Wilsbacher 2.2k 1.1× 700 1.1× 470 0.8× 192 0.5× 158 0.4× 31 3.1k
Kurt R. Auger 4.1k 2.0× 1.3k 2.1× 1.0k 1.8× 405 1.1× 233 0.6× 33 5.4k
Ami Aronheim 3.0k 1.4× 553 0.9× 838 1.4× 279 0.7× 193 0.5× 80 3.9k
Johannes Schlöndorff 1.8k 0.9× 759 1.2× 354 0.6× 404 1.1× 227 0.6× 39 3.2k
Bart Vanhaesebroeck 2.7k 1.3× 682 1.1× 588 1.0× 284 0.7× 175 0.5× 17 3.8k

Countries citing papers authored by Christopher Winter

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Winter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher Winter. 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 Christopher Winter. The network helps show where Christopher Winter may publish in the future.

Co-authorship network of co-authors of Christopher Winter

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Winter. A scholar is included among the top collaborators of Christopher Winter 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 Christopher Winter. Christopher Winter 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.
Kerns, J. William, Danya M. Qato, Katherine Winter, et al.. (2025). Clinician Perspectives on Increased Gabapentinoid Prescribing in Nursing Homes. Journal of the American Geriatrics Society. 73(6). 1953–1956.
2.
Dahl, Jesper, Christopher Winter, Veit Rothhammer, et al.. (2025). Modulator of VRAC Current 1 Is a Potential Target Antigen in Multiple Sclerosis. Neurology Neuroimmunology & Neuroinflammation. 12(2). e200374–e200374. 4 indexed citations
3.
Yuan, Lin, Meghana Kulkarni, Evan L. Chiswick, et al.. (2025). A novel approach for first‐in‐human dose selection using population dose–response modelling to find a minimum anticipated biological effect level. British Journal of Clinical Pharmacology. 91(9). 2555–2566.
4.
Kerns, J. William, Nicole Brandt, Danya M. Qato, et al.. (2024). Prescribing Trends and Associated Outcomes of Antiepileptic Drugs and Other Psychotropic Medications in US Nursing Homes: Proposal for a Mixed Methods Investigation. JMIR Research Protocols. 13. e64446–e64446.
6.
Kerns, J. William, Danya M. Qato, Katherine Winter, et al.. (2024). A Nursing Home Clinician Survey to Explain Gabapentinoid Increases. Journal of the American Medical Directors Association. 26(1). 105363–105363. 1 indexed citations
7.
Long, Richard, et al.. (2023). Limitations of Chest Radiography in Diagnosing Subclinical Pulmonary Tuberculosis in Canada. SHILAP Revista de lepidopterología. 7(3). 165–170. 3 indexed citations
8.
Lau, Angela, Christopher Lin, Christopher Winter, et al.. (2022). A comparison of the chest radiographic and computed tomographic features of subclinical pulmonary tuberculosis. Scientific Reports. 12(1). 16567–16567. 6 indexed citations
9.
10.
O’Neil, Jennifer, Yair Benita, Igor Feldman, et al.. (2016). An Unbiased Oncology Compound Screen to Identify Novel Combination Strategies. Molecular Cancer Therapeutics. 15(6). 1155–1162. 227 indexed citations
11.
Lau, Angela, et al.. (2016). Chest Radiographic Patterns and the Transmission of Tuberculosis: Implications for Automated Systems. PLoS ONE. 11(4). e0154032–e0154032. 20 indexed citations
12.
Hagel, Margit, Chandra Miduturu, Michael P. Sheets, et al.. (2015). First Selective Small Molecule Inhibitor of FGFR4 for the Treatment of Hepatocellular Carcinomas with an Activated FGFR4 Signaling Pathway. Cancer Discovery. 5(4). 424–437. 247 indexed citations
13.
Cosimo, Serena Di, Sriram Sathyanarayanan, Johanna C. Bendell, et al.. (2014). Combination of the mTOR Inhibitor Ridaforolimus and the Anti-IGF1R Monoclonal Antibody Dalotuzumab: Preclinical Characterization and Phase I Clinical Trial. Clinical Cancer Research. 21(1). 49–59. 48 indexed citations
14.
Efferson, Clay L., Christopher T. Winkelmann, Christopher Ware, et al.. (2010). Downregulation of Notch Pathway by a γ-Secretase Inhibitor Attenuates AKT/Mammalian Target of Rapamycin Signaling and Glucose Uptake in an ERBB2 Transgenic Breast Cancer Model. Cancer Research. 70(6). 2476–2484. 76 indexed citations
15.
Watters, James, Chun Cheng, Pradip K. Majumder, et al.. (2009). De novo Discovery of a γ-Secretase Inhibitor Response Signature Using a Novel In vivo Breast Tumor Model. Cancer Research. 69(23). 8949–8957. 31 indexed citations
16.
Rao, Sudhir, Jennifer O’Neil, James S. Hardwick, et al.. (2009). Inhibition of NOTCH Signaling by Gamma Secretase Inhibitor Engages the RB Pathway and Elicits Cell Cycle Exit in T-Cell Acute Lymphoblastic Leukemia Cells. Cancer Research. 69(7). 3060–3068. 114 indexed citations
17.
O’Neil, Jennifer, Jonathan Grim, Peter R. Strack, et al.. (2007). FBW7 mutations in leukemic cells mediate NOTCH pathway activation and resistance to γ-secretase inhibitors. The Journal of Experimental Medicine. 204(8). 1813–1824. 523 indexed citations breakdown →
18.
Parks, Annette L., David A. Ruddy, Stanley Tiong, et al.. (2006). Presenilin-Based Genetic Screens in Drosophila melanogaster Identify Novel Notch Pathway Modifiers. Genetics. 172(4). 2309–2324. 41 indexed citations
19.
Billuart, Pierre, et al.. (2001). Regulating Axon Branch Stability. Cell. 107(2). 195–207. 178 indexed citations
20.
Winter, Christopher, Bruce Wang, Anne Royou, et al.. (2001). Drosophila Rho-Associated Kinase (Drok) Links Frizzled-Mediated Planar Cell Polarity Signaling to the Actin Cytoskeleton. Cell. 105(1). 81–91. 451 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

Rankless by CCL
2026