Daniel Pinkel

29.4k total citations · 6 hit papers
146 papers, 18.0k citations indexed

About

Daniel Pinkel is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Daniel Pinkel has authored 146 papers receiving a total of 18.0k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Genetics, 79 papers in Molecular Biology and 41 papers in Plant Science. Recurrent topics in Daniel Pinkel's work include Genomic variations and chromosomal abnormalities (74 papers), Chromosomal and Genetic Variations (39 papers) and Cancer Genomics and Diagnostics (22 papers). Daniel Pinkel is often cited by papers focused on Genomic variations and chromosomal abnormalities (74 papers), Chromosomal and Genetic Variations (39 papers) and Cancer Genomics and Diagnostics (22 papers). Daniel Pinkel collaborates with scholars based in United States, Netherlands and Japan. Daniel Pinkel's co-authors include Joe W. Gray, Donna G. Albertson, T. Straume, Boris C. Bastian, Klaus J. Busam, John A. Curtin, Antoine M. Snijders, Richard Segraves, Philip E. LeBoit and Evan E. Eichler and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and JAMA.

In The Last Decade

Daniel Pinkel

142 papers receiving 17.4k citations

Hit Papers

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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.

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

1986 2.7k citations Daniel Pinkel, T. Straume et al. profile →
Somatic Activation of KIT in Distinct Subtypes of Melanoma

2006 1.1k citations John A. Curtin, Klaus J. Busam et al. Journal of Clinical Oncology profile →
PIK3CA is implicated as an oncogene in ovarian cancer

1999 925 citations Daniel Pinkel, Joe W. Gray et al. profile →
Fine-scale structural variation of the human genome

2005 742 citations Andrew J. Sharp, Jeffrey A. Bailey et al. profile →
Assembly of microarrays for genome-wide measurement of DNA copy number

2001 712 citations Antoine M. Snijders, Norma J. Nowak et al. profile →
Segmental Duplications and Copy-Number Variation in the Human Genome

2005 678 citations Andrew J. Sharp, Devin P. Locke et al. The American Journal of Human Genetics profile →

Author Peers

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

Author						Papers	Cites
Daniel Pinkel	10.5k	7.6k	4.1k	3.8k	3.3k	146	18.0k
Thomas Ried	17.7k 1.7×	6.2k 0.8×	2.8k 0.7×	7.3k 1.9×	6.2k 1.9×	378	27.8k
Maria Jasin	24.8k 2.4×	5.6k 0.7×	3.5k 0.9×	6.7k 1.8×	4.1k 1.2×	206	27.4k
Donna G. Albertson	9.4k 0.9×	5.9k 0.8×	2.5k 0.6×	2.4k 0.6×	2.9k 0.9×	164	16.2k
Bernard Dutrillaux	8.0k 0.8×	4.5k 0.6×	2.7k 0.7×	2.9k 0.8×	2.7k 0.8×	407	13.1k
Colin C. Collins	10.2k 1.0×	4.6k 0.6×	1.8k 0.4×	2.6k 0.7×	4.5k 1.3×	201	16.6k
Mark H. Skolnick	6.5k 0.6×	6.4k 0.9×	2.9k 0.7×	3.4k 0.9×	1.9k 0.6×	141	17.3k
Michael R. Speicher	10.0k 0.9×	4.2k 0.6×	2.2k 0.5×	5.7k 1.5×	6.5k 2.0×	177	19.1k
Mark Groudine	27.1k 2.6×	6.2k 0.8×	3.8k 0.9×	3.0k 0.8×	1.9k 0.6×	223	32.6k
Yusuke Nakamura	11.8k 1.1×	5.7k 0.8×	795 0.2×	5.2k 1.4×	3.4k 1.0×	426	22.7k
Erich A. Nigg	35.4k 3.4×	5.1k 0.7×	3.9k 1.0×	8.5k 2.3×	1.7k 0.5×	262	42.6k

Countries citing papers authored by Daniel Pinkel

Since Specialization

Citations

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

Fields of papers citing papers by Daniel Pinkel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Pinkel

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

All Works

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20 of 20 papers shown

Scheinin, Ilari, Daoud Sie, Henrik Bengtsson, et al.. (2014). DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly. Genome Research. 24(12). 2022–2032. 265 indexed citations

Bhattacharya, Aditi, Ritu Roy, Antoine M. Snijders, et al.. (2011). Two Distinct Routes to Oral Cancer Differing in Genome Instability and Risk for Cervical Node Metastasis. Clinical Cancer Research. 17(22). 7024–7034. 55 indexed citations

North, Jeffrey P., Toshiro Kageshita, Daniel Pinkel, Philip E. LeBoit, & Boris C. Bastian. (2008). Distribution and Significance of Occult Intraepidermal Tumor Cells Surrounding Primary Melanoma. Journal of Investigative Dermatology. 128(8). 2024–2030. 60 indexed citations

Climent, Joan, Jane Fridlyand, José Palacios, et al.. (2007). Deletion of Chromosome 11q Predicts Response to Anthracycline-Based Chemotherapy in Early Breast Cancer. Cancer Research. 67(2). 818–826. 67 indexed citations

Snijders, Antoine M., Serena S. Kwek, Ritu Roydasgupta, et al.. (2007). Genome position and gene amplification. Genome biology. 8(6). R120–R120. 21 indexed citations

Tomioka, Nobumoto, Shinya Oba, Miki Ohira, et al.. (2007). Novel risk stratification of patients with neuroblastoma by genomic signature, which is independent of molecular signature. Oncogene. 27(4). 441–449. 66 indexed citations

Curtin, John A., Klaus J. Busam, Daniel Pinkel, & Boris C. Bastian. (2006). Somatic Activation of KIT in Distinct Subtypes of Melanoma. Journal of Clinical Oncology. 24(26). 4340–4346. 1124 indexed citations breakdown →

Landi, Maria Teresa, Jürgen Bauer, Ruth M. Pfeiffer, et al.. (2006). MC1R Germline Variants Confer Risk for BRAF -Mutant Melanoma. Science. 313(5786). 521–522. 238 indexed citations

Locke, Devin P., Andrew J. Sharp, Steven A. McCarroll, et al.. (2006). Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome. The American Journal of Human Genetics. 79(2). 275–290. 231 indexed citations

10.

Sharp, Andrew J., Devin P. Locke, Sean McGrath, et al.. (2005). Segmental Duplications and Copy-Number Variation in the Human Genome. The American Journal of Human Genetics. 77(1). 78–88. 678 indexed citations breakdown →

11.

Snijders, Antoine M., Norma J. Nowak, Bing Huey, et al.. (2005). Mapping segmental and sequence variations among laboratory mice using BAC array CGH. Genome Research. 15(2). 302–311. 65 indexed citations

12.

Leamon, John H., Tanja Pejović, Stefan Hamann, et al.. (2003). Whole Genome Analysis of Genetic Alterations in Small DNA Samples Using Hyperbranched Strand Displacement Amplification and Array–CGH. Genome Research. 13(2). 294–307. 212 indexed citations

13.

Locke, Devin P., Richard Segraves, Lucia Carbone, et al.. (2003). Large-Scale Variation Among Human and Great Ape Genomes Determined by Array Comparative Genomic Hybridization. Genome Research. 13(3). 347–357. 105 indexed citations

14.

Snijders, Antoine M., Jane Fridlyand, Dorus A. Mans, et al.. (2003). Shaping of tumor and drug-resistant genomes by instability and selection. Oncogene. 22(28). 4370–4379. 61 indexed citations

15.

Jain, Ajay N., Taku A. Tokuyasu, Antoine M. Snijders, et al.. (2002). Fully Automatic Quantification of Microarray Image Data. Genome Research. 12(2). 325–332. 269 indexed citations

16.

Andreeff, Michael & Daniel Pinkel. (1999). Introduction to fluorescence in situ hybridization : principles and clinical applications. Wiley eBooks. 33 indexed citations

17.

Robbins, Wendie A., Richard Segraves, Daniel Pinkel, & Andrew J. Wyrobek. (1993). Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y.. Europe PMC (PubMed Central). 52(4). 799–807. 132 indexed citations

18.

Lucas, J. N., T. Straume, Daniel Pinkel, et al.. (1989). Rapid Human Chromosome Aberration Analysis Using Fluorescence in Situ Hybridization. International Journal of Radiation Biology. 56(1). 35–44. 167 indexed citations

19.

Dean, Phillip N., et al.. (1981). The Livermore flow cytometer. NASA STI/Recon Technical Report N. 83. 16721. 5 indexed citations

20.

Pinkel, Daniel. (1981). On the possibility of automated scoring of pollen mutants.. Environmental Health Perspectives. 37. 133–136. 2 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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