Christa M. Lese

788 total citations
12 papers, 598 citations indexed

About

Christa M. Lese is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christa M. Lese has authored 12 papers receiving a total of 598 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christa M. Lese's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and RNA modifications and cancer (3 papers). Christa M. Lese is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and RNA modifications and cancer (3 papers). Christa M. Lese collaborates with scholars based in United States, Canada and United Kingdom. Christa M. Lese's co-authors include David H. Ledbetter, Susanne M. Gollin, Kathrin S. Precht, Harold Riethman, Thomas J. Hudson, N. M. Lawrie, Jonathan Flint, Regina Regan, D. L. N. Cardy and A Nicod and has published in prestigious journals such as Genome Research, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Christa M. Lese

12 papers receiving 582 citations

Author Peers

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

Author Last Decade Papers Cites
Christa M. Lese 438 313 168 157 68 12 598
Jiangzhen Li 751 1.7× 418 1.3× 217 1.3× 294 1.9× 39 0.6× 8 946
E. Orye 311 0.7× 233 0.7× 122 0.7× 137 0.9× 65 1.0× 35 590
Judith Dagan 223 0.5× 231 0.7× 88 0.5× 96 0.6× 39 0.6× 27 457
M. F. Croquette 293 0.7× 274 0.9× 100 0.6× 49 0.3× 45 0.7× 17 444
D. C. Burford 394 0.9× 324 1.0× 210 1.3× 70 0.4× 49 0.7× 6 583
Anita S. Kulharya 452 1.0× 509 1.6× 106 0.6× 147 0.9× 26 0.4× 31 843
Philippe Coullin 208 0.5× 268 0.9× 76 0.5× 189 1.2× 23 0.3× 28 526
M.M. Aronson 213 0.5× 264 0.8× 83 0.5× 90 0.6× 45 0.7× 48 498
J L Watt 298 0.7× 191 0.6× 130 0.8× 161 1.0× 23 0.3× 19 462
H. Reinwein 640 1.5× 377 1.2× 216 1.3× 174 1.1× 20 0.3× 54 782

Countries citing papers authored by Christa M. Lese

Since Specialization
Citations

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

Fields of papers citing papers by Christa M. Lese

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christa M. Lese. 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 Christa M. Lese. The network helps show where Christa M. Lese may publish in the future.

Co-authorship network of co-authors of Christa M. Lese

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

All Works

12 of 12 papers shown
1.
Tepperberg, James, Mark J. Pettenati, P. Nagesh Rao, et al.. (2001). Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2‐year multi‐center retrospective study and review of the literature. Prenatal Diagnosis. 21(4). 293–301. 89 indexed citations
2.
Knight, Samantha J.L., Christa M. Lese, Kathrin S. Precht, et al.. (2000). An Optimized Set of Human Telomere Clones for Studying Telomere Integrity and Architecture. The American Journal of Human Genetics. 67(2). 320–332. 237 indexed citations
3.
Das, Soma, Christa M. Lese, Minsun Song, et al.. (2000). Partial Paternal Uniparental Disomy of Chromosome 6 in an Infant with Neonatal Diabetes, Macroglossia, and Craniofacial Abnormalities. The American Journal of Human Genetics. 67(6). 1586–1591. 27 indexed citations
4.
Kaiser‐Rogers, Kathleen, Kathleen W. Rao, Ron C. Michaelis, Christa M. Lese, & Cynthia M. Powell. (2000). Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements. American Journal of Medical Genetics. 95(1). 28–35. 5 indexed citations
5.
Shuster, Michèle, Limin Han, Michelle M. Le Beau, et al.. (2000). A consistent pattern ofRIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage-fusion-bridge cycle model for 11q13 amplification. Genes Chromosomes and Cancer. 28(2). 153–163. 88 indexed citations
6.
Shuster, Michèle, Limin Han, Michelle M. Le Beau, et al.. (2000). A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage‐fusion‐bridge cycle model for 11q13 amplification. Genes Chromosomes and Cancer. 28(2). 153–163. 3 indexed citations
7.
Lese, Christa M., Judy Fantes, Harold Riethman, & David H. Ledbetter. (1999). Characterization of Physical Gap Sizes at Human Telomeres. Genome Research. 9(9). 888–894. 18 indexed citations
8.
McLaughlin, Mark R., Susanne M. Gollin, Christa M. Lese, & A. Leland Albright. (1998). Medulloblastoma and Glioblastoma Multiforme in a Patient with Turcot Syndrome: A Case Report. Surgical Neurology. 49(3). 295–301. 15 indexed citations
9.
Precht, Kathrin S., Christa M. Lese, Rhonda Spiro, et al.. (1998). Two 22q telomere deletions serendipitously detected by FISH.. Journal of Medical Genetics. 35(11). 939–942. 55 indexed citations
10.
Lese, Christa M., Judith A. Fantes, Kathrin S. Precht, et al.. (1997). Molecular characterization of human telomeres: extension of integrated physical maps and strategies for genotype-phenotype correlations.. Oxford University Research Archive (ORA) (University of Oxford). 1 indexed citations
11.
Lese, Christa M., Karen Rossie, Billy N. Appel, et al.. (1995). Visualization of INT2 and HST1 Amplification in oral squamous cell carcinomas. Genes Chromosomes and Cancer. 12(4). 288–295. 59 indexed citations
12.
Lese, Christa M., Susanne M. Gollin, & Karen Rossie. (1994). Visualization of INT2 and HST1 amplification in oral squamous cell carcinoma. The American Journal of Human Genetics. 55. 1 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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