Patrick A. Lennon

1.1k total citations
32 papers, 802 citations indexed

About

Patrick A. Lennon is a scholar working on Genetics, Pathology and Forensic Medicine and Hematology. According to data from OpenAlex, Patrick A. Lennon has authored 32 papers receiving a total of 802 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Pathology and Forensic Medicine and 11 papers in Hematology. Recurrent topics in Patrick A. Lennon's work include Lymphoma Diagnosis and Treatment (9 papers), Acute Myeloid Leukemia Research (8 papers) and Chronic Lymphocytic Leukemia Research (7 papers). Patrick A. Lennon is often cited by papers focused on Lymphoma Diagnosis and Treatment (9 papers), Acute Myeloid Leukemia Research (8 papers) and Chronic Lymphocytic Leukemia Research (7 papers). Patrick A. Lennon collaborates with scholars based in United States, United Kingdom and Canada. Patrick A. Lennon's co-authors include L. Jeffrey Medeiros, Pei Lin, Roberto N. Miranda, Luis Fayad, C. Cameron Yin, E. Lin, Shaoying Li, Peter Hu, Francisco Vega and Sau Wai Cheung and has published in prestigious journals such as Blood, Cancer and Cancer Research.

In The Last Decade

Patrick A. Lennon

32 papers receiving 779 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick A. Lennon United States 14 350 293 255 242 188 32 802
Kumi Nakazaki Japan 10 130 0.4× 143 0.5× 543 2.1× 154 0.6× 209 1.1× 34 996
JJ Cassiman Belgium 10 273 0.8× 180 0.6× 110 0.4× 136 0.6× 84 0.4× 19 572
GJ van Ommen Netherlands 9 254 0.7× 155 0.5× 167 0.7× 156 0.6× 156 0.8× 13 494
Judith E. Powell United Kingdom 13 233 0.7× 357 1.2× 197 0.8× 229 0.9× 69 0.4× 17 711
Christine Pérot France 17 75 0.2× 175 0.6× 357 1.4× 124 0.5× 441 2.3× 31 934
Katarina Reinhardt Germany 13 115 0.3× 80 0.3× 211 0.8× 67 0.3× 318 1.7× 20 551
Hidemitsu Kurosawa Japan 14 52 0.1× 176 0.6× 373 1.5× 146 0.6× 339 1.8× 59 827
Amanda R. Perry United Kingdom 11 311 0.9× 135 0.5× 172 0.7× 208 0.9× 93 0.5× 13 726
Takahiro Itoyama Japan 16 160 0.5× 94 0.3× 248 1.0× 85 0.4× 92 0.5× 42 672
K Longin United States 12 84 0.2× 212 0.7× 113 0.4× 456 1.9× 870 4.6× 18 1.1k

Countries citing papers authored by Patrick A. Lennon

Since Specialization
Citations

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

Fields of papers citing papers by Patrick A. Lennon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick A. Lennon

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick A. Lennon. A scholar is included among the top collaborators of Patrick A. Lennon 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 A. Lennon. Patrick A. Lennon 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.
Levy, Brynn, Linda B. Baughn, Yassmine Akkari, et al.. (2022). Optical genome mapping in acute myeloid leukemia: a multicenter evaluation. Blood Advances. 7(7). 1297–1307. 65 indexed citations
2.
Mukherjee, Sandeep, Scott R. Wheeler, Malini Sathanoori, et al.. (2016). Chromosomal microarray provides enhanced targetable gene aberration detection when paired with next generation sequencing panel in profiling lung and colorectal tumors. Cancer Genetics. 209(4). 119–129. 6 indexed citations
3.
Singh, Rajesh R., Kranthi Kunkalla, Yadong Liu, et al.. (2012). Defining causative factors contributing in the activation of hedgehog signaling in diffuse large B-cell lymphoma. Leukemia Research. 36(10). 1267–1273. 7 indexed citations
4.
Lennon, Patrick A., et al.. (2012). Is monosomy 21 rare? Seven early miscarriages including one mosaic 45,XX,‐21/44,X,‐21 in a single study population. American Journal of Medical Genetics Part A. 158A(8). 2050–2052. 5 indexed citations
5.
Hu, Peter, Patrick A. Lennon, & Madhuri Hegde. (2012). Modern Clinical Molecular Techniques. Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)). 11 indexed citations
6.
7.
8.
Li, Ting, L. Jeffrey Medeiros, Pei Lin, et al.. (2010). Immunohistochemical profile and fluorescence in situ hybridization analysis of diffuse large B-cell lymphoma in northern China.. Archives of Pathology & Laboratory Medicine. 134(5). 759–65. 7 indexed citations
9.
Lennon, Patrick A., Srđan Verstovšek, Bedia A. Barkoh, et al.. (2010). Distinct patterns of cytogenetic and clinical progression in chronic myeloproliferative neoplasms with or without JAK2 or MPL mutations. Cancer Genetics and Cytogenetics. 197(1). 1–7. 14 indexed citations
10.
Li, Ting, L. Jeffrey Medeiros, Pei Lin, et al.. (2010). Immunohistochemical Profile and Fluorescence In Situ Hybridization Analysis of Diffuse Large B-Cell Lymphoma in Northern China. Archives of Pathology & Laboratory Medicine. 134(5). 759–765. 6 indexed citations
11.
Singh, Rajesh R., Jeong Hee Cho‐Vega, Shuguang Ma, et al.. (2009). Sonic Hedgehog Signaling Pathway Is Activated in ALK-Positive Anaplastic Large Cell Lymphoma. Cancer Research. 69(6). 2550–2558. 74 indexed citations
12.
Lin, Pei, et al.. (2008). Translocation (18;22)(q21;q11) in B-cell lymphomas: a report of 4 cases and review of the literature. Human Pathology. 39(11). 1664–1672. 13 indexed citations
13.
Quintás‐Cardama, Alfonso, Taghi Manshouri, Francisco Vega, et al.. (2008). Activity of tyrosine kinase inhibitors against human NUP214-ABL1-positive T cell malignancies. Leukemia. 22(6). 1117–1124. 66 indexed citations
14.
Lennon, Patrick A., Lynne V. Abruzzo, L. Jeffrey Medeiros, et al.. (2007). Aberrant EVI1 expression in acute myeloid leukemias associated with the t(3;8)(q26;q24). Cancer Genetics and Cytogenetics. 177(1). 37–42. 21 indexed citations
15.
Lennon, Patrick A., M. Lance Cooper, Daniel A. Peiffer, et al.. (2007). Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review. American Journal of Medical Genetics Part A. 143A(8). 791–798. 62 indexed citations
16.
Konoplev, Sergej, et al.. (2007). Therapy may unmask hypoplastic myelodysplastic syndrome that mimics aplastic anemia. Cancer. 110(7). 1520–1526. 14 indexed citations
17.
Lennon, Patrick A., Daryl A. Scott, David S. Wargowski, et al.. (2006). WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH. American Journal of Medical Genetics Part A. 140A(11). 1214–1218. 9 indexed citations
18.
Lennon, Patrick A., M. Lance Cooper, Cynthia Lim, et al.. (2006). Array‐based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation. American Journal of Medical Genetics Part A. 140A(11). 1156–1163. 3 indexed citations
19.
Lennon, Patrick A., et al.. (2006). A novel 8.5 MB dup(1)(p34.1p34.3) characterized by FISH in a child presenting with congenital heart defect and dysmorphic features. American Journal of Medical Genetics Part A. 140A(17). 1864–1870. 2 indexed citations
20.
Pearson, Margaret A., Paweł Stankiewicz, Patrick A. Lennon, et al.. (2005). Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array‐based comparative genomic hybridization in a patient with mental retardation and dysmorphic features. American Journal of Medical Genetics Part A. 137A(1). 88–93. 7 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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