Constance A. Griffin

14.5k total citations · 2 hit papers
140 papers, 8.8k citations indexed

About

Constance A. Griffin is a scholar working on Molecular Biology, Oncology and Pathology and Forensic Medicine. According to data from OpenAlex, Constance A. Griffin has authored 140 papers receiving a total of 8.8k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 43 papers in Oncology and 34 papers in Pathology and Forensic Medicine. Recurrent topics in Constance A. Griffin's work include Genetic factors in colorectal cancer (20 papers), Cancer Genomics and Diagnostics (19 papers) and Pancreatic and Hepatic Oncology Research (15 papers). Constance A. Griffin is often cited by papers focused on Genetic factors in colorectal cancer (20 papers), Cancer Genomics and Diagnostics (19 papers) and Pancreatic and Hepatic Oncology Research (15 papers). Constance A. Griffin collaborates with scholars based in United States, Netherlands and Thailand. Constance A. Griffin's co-authors include Anita L. Hawkins, Ralph H. Hruban, Elizabeth J. Perlman, Gloria M. Petersen, Kieran Brune, Antonio M. Persico, Laura Morsberger, Charles J. Yeo, Patricia P. Long and Ethylin Wang Jabs and has published in prestigious journals such as Proceedings of the National Academy of Sciences, JAMA and Journal of Biological Chemistry.

In The Last Decade

Constance A. Griffin

140 papers receiving 8.5k 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.

Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR

1992 586 citations Anita L. Hawkins, Constance A. Griffin et al. Genomics profile →
Haploinsufficiency of t e lomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita

2005 324 citations Mary Armanios, Julian J.‐L. Chen et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Constance A. Griffin United States	47	3.2k	3.2k	1.7k	1.4k	1.3k	140	8.8k
Bruce G. Robinson Australia	56	2.2k 0.7×	3.4k 1.0×	2.6k 1.5×	3.0k 2.1×	1.3k 1.0×	227	11.3k
Nobutaka Shimizu Japan	41	2.2k 0.7×	3.0k 0.9×	802 0.5×	654 0.5×	2.4k 1.7×	224	8.0k
Reinhard Buettner Germany	60	3.4k 1.0×	8.9k 2.8×	2.1k 1.3×	1.3k 0.9×	2.3k 1.7×	312	14.3k
Virginia V. Michels United States	47	1.2k 0.4×	3.1k 1.0×	1.2k 0.7×	1.3k 0.9×	914 0.7×	148	9.1k
Lisa Cannon‐Albright United States	45	2.8k 0.9×	2.2k 0.7×	1.6k 1.0×	943 0.7×	1.2k 0.9×	223	8.0k
Robert F. Gagel United States	58	4.7k 1.4×	3.6k 1.1×	1.6k 0.9×	3.9k 2.8×	1.3k 0.9×	221	14.7k
Mario Serio Italy	48	2.1k 0.7×	2.8k 0.9×	644 0.4×	1.2k 0.8×	803 0.6×	151	8.2k
Robert M.W. Hofstra Netherlands	60	2.7k 0.8×	5.1k 1.6×	2.0k 1.2×	3.4k 2.4×	1.2k 0.9×	251	12.9k
Thierry Frébourg France	60	4.5k 1.4×	6.5k 2.0×	2.5k 1.5×	934 0.7×	1.4k 1.1×	276	14.1k
Qin Huang United States	47	1.9k 0.6×	3.1k 1.0×	1.1k 0.7×	1.7k 1.2×	1.4k 1.1×	288	7.6k

Countries citing papers authored by Constance A. Griffin

Since Specialization

Citations

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

Fields of papers citing papers by Constance A. Griffin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Constance A. Griffin

This figure shows the co-authorship network connecting the top 25 collaborators of Constance A. Griffin. A scholar is included among the top collaborators of Constance A. Griffin 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 Constance A. Griffin. Constance A. Griffin 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

Showel, Margaret M., Robert A. Brodsky, Hua-Ling Tsai, et al.. (2014). Isolated Clonal Cytogenetic Abnormalities after High-Dose Therapy. Biology of Blood and Marrow Transplantation. 20(8). 1130–1138. 3 indexed citations

Edelstein, Daniel L., Jennifer E. Axilbund, Linda M. Hylind, et al.. (2012). Serrated polyposis: rapid and relentless development of colorectal neoplasia. Gut. 62(3). 404–408. 69 indexed citations

Neklason, Deborah W., Ann G. Schwartz, Hoda Anton‐Culver, et al.. (2011). Activating mutation in MET oncogene in familial colorectal cancer. BMC Cancer. 11(1). 424–424. 37 indexed citations

Edelstein, Daniel L., Jennifer E. Axilbund, Linda M. Hylind, et al.. (2010). Rapid Development of Colorectal Neoplasia in Patients With Lynch Syndrome. Clinical Gastroenterology and Hepatology. 9(4). 340–343. 92 indexed citations

Wu, Julie M., Mary Jo Fackler, Marc K. Halushka, et al.. (2008). Heterogeneity of Breast Cancer Metastases: Comparison of Therapeutic Target Expression and Promoter Methylation Between Primary Tumors and Their Multifocal Metastases. Clinical Cancer Research. 14(7). 1938–1946. 165 indexed citations

Neklason, Deborah W., Richard A. Kerber, Hoda Anton‐Culver, et al.. (2008). Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis. Cancer Research. 68(21). 8993–8997. 27 indexed citations

Panagopoulos, Ioannis, Fredrik Mertens, & Constance A. Griffin. (2008). An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera. Cancer Genetics and Cytogenetics. 185(2). 74–77. 33 indexed citations

Griffin, Constance A., Peter C. Burger, Laura Morsberger, et al.. (2006). Identification of der(1;19)(q10;p10) in Five Oligodendrogliomas Suggests Mechanism of Concurrent 1p and 19q Loss. Journal of Neuropathology & Experimental Neurology. 65(10). 988–994. 215 indexed citations

Armanios, Mary, Julian J.‐L. Chen, Yen-Pei C. Chang, et al.. (2005). Haploinsufficiency of t e lomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita. Proceedings of the National Academy of Sciences. 102(44). 15960–15964. 324 indexed citations breakdown →

10.

Henkle, C, Anita L. Hawkins, Edward F. McCarthy, & Constance A. Griffin. (2004). Clear cell sarcoma case report: Complex karyotype including t(12;22) in primary and metastatic tumor. Cancer Genetics and Cytogenetics. 149(1). 63–67. 6 indexed citations

11.

Kline, Antonie D., Constance A. Griffin, Mary Haddadin, et al.. (2004). A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies. American Journal of Medical Genetics Part A. 129A(2). 124–129. 4 indexed citations

12.

Johnson, Karen A., Jill D. Trimbath, Gloria M. Petersen, Constance A. Griffin, & Francis M. Giardiello. (2002). Impact of Genetic Counseling and Testing on Colorectal Cancer Screening Behavior. Genetic Testing. 6(4). 303–306. 40 indexed citations

13.

Chou, Wen‐Chien, Anita L. Hawkins, John F. Barrett, Constance A. Griffin, & Chi V. Dang. (2001). Arsenic inhibition of telomerase transcription leads to genetic instability. Journal of Clinical Investigation. 108(10). 1541–1547. 106 indexed citations

14.

Gladstone, Douglas E., Atul Bedi, Carole B. Miller, et al.. (1999). Philadelphia chromosome-negative engraftment after autologous transplantation with granulocyte-macrophage colony-stimulating factor for chronic myeloid leukemia. Biology of Blood and Marrow Transplantation. 5(6). 394–399. 11 indexed citations

15.

Levenstein, Mark E., et al.. (1999). SZF1. Experimental Hematology. 27(2). 313–325. 16 indexed citations

16.

Perlman, Elizabeth J., Marcus B. Valentine, Constance A. Griffin, & A. Thomas Look. (1996). Deletion of Ip36 in childhood endodermal sinus tumors by two-color fluorescence in situ hybridization: A pediatric oncology group study. Genes Chromosomes and Cancer. 16(1). 15–20. 42 indexed citations

17.

Perlman, Elizabeth J., Barbara Cushing, Edith P. Hawkins, & Constance A. Griffin. (1994). Cytogenetic Analysis of Childhood Endodermal Sinus Tumors: A Pediatric Oncology Group Study. Pediatric Pathology. 14(4). 695–708. 56 indexed citations

18.

McGregor, Lisa M., Stephen B. Baylin, Constance A. Griffin, Anita L. Hawkins, & Barry D. Nelkin. (1994). Molecular Cloning of the cDNA for Human TrkC (NTRK3), Chromosomal Assignment, and Evidence for a Splice Variant. Genomics. 22(2). 267–272. 31 indexed citations

19.

Griffin, Constance A., et al.. (1993). Human Rod cGMP-Gated Cation Channel Gene Maps to 4p12 → Centromere by Chromosomal in Situ Hybridization. Genomics. 16(1). 302–303. 3 indexed citations

20.

Hawkins, Anita L., et al.. (1992). Fluorescence in situ hybridization to determine engraftment status after murine bone marrow transplant. Cancer Genetics and Cytogenetics. 64(2). 145–148. 26 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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