Roger V. Lebo

6.3k total citations · 2 hit papers
70 papers, 5.0k citations indexed

About

Roger V. Lebo is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Roger V. Lebo has authored 70 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 34 papers in Genetics and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Roger V. Lebo's work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (12 papers) and Chromosomal and Genetic Variations (10 papers). Roger V. Lebo is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (12 papers) and Chromosomal and Genetic Variations (10 papers). Roger V. Lebo collaborates with scholars based in United States, Germany and China. Roger V. Lebo's co-authors include Ronald M. Evans, Cary Weinberger, Estelita S. Ong, Catherine C. Thompson, Donald J. Gruol, Anthony E. Oro, Stanley M. Hollenberg, Michael G. Rosenfeld, E. Brad Thompson and Barry D. Bruce and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Roger V. Lebo

68 papers receiving 4.8k 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.

Primary structure and expression of a functional human glucocorticoid receptor cDNA

1985 1.5k citations Roger V. Lebo et al. profile →
The c-erb-A gene encodes a thyroid hormone receptor

1986 1.3k citations Roger V. Lebo et al. profile →

Peers

Roger V. Lebo

GENET

MB

EDM

IMMUN

CMN

Micheline Misrahi France

Bogi Andersen United States

Claude Szpirer Belgium

Enzo Lalli France

Maria D. Lalioti United States

Anatoli S. Gleiberman United States

Catherine C. Thompson United States

Kaoru Miyamoto Japan

Kenneth W. Gross United States

Jun Kudoh Japan

Micheline Misrahi France

Roger V. Lebo

2.3k ×1.0

GENET

3.0k ×1.3

MB

1.8k ×1.1

EDM

729 ×1.4

IMMUN

660 ×1.4

CMN

Citations per year, relative to Roger V. Lebo Roger V. Lebo (= 1×) peers Micheline Misrahi

Countries citing papers authored by Roger V. Lebo

Since Specialization

Citations

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

Fields of papers citing papers by Roger V. Lebo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roger V. Lebo. 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 Roger V. Lebo. The network helps show where Roger V. Lebo may publish in the future.

Co-authorship network of co-authors of Roger V. Lebo

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Grody, Wayne W., Barry H. Thompson, Anthony R. Gregg, et al.. (2013). ACMG Position Statement on Prenatal/Preconception Expanded Carrier Screening. Obstetrical & Gynecological Survey. 68(12). 785–787. 5 indexed citations

2.

Grody, Wayne W., Barry H. Thompson, Anthony R. Gregg, et al.. (2013). ACMG position statement on prenatal/preconception expanded carrier screening. Genetics in Medicine. 15(6). 482–483. 173 indexed citations

3.

Lebo, Roger V. & Wayne W. Grody. (2007). Variable Penetrance And Expressivity of The Splice Altering 5T Sequence in The Cystic Fibrosis Gene. Genetic Testing. 11(1). 32–44. 10 indexed citations

4.

Lebo, Roger V. & Wayne W. Grody. (2007). Testing and Reporting ACMG Cystic Fibrosis Mutation Panel Results. Genetic Testing. 11(1). 11–31. 16 indexed citations

5.

Lebo, Roger V. & Gregory J. Omlor. (2007). Targeted Extended Cystic Fibrosis Mutation Testing on Known and At-Risk Patients and Relatives. Genetic Testing. 11(4). 427–444. 2 indexed citations

6.

Lebo, Roger V., et al.. (2007). One Multiplex Control for 29 Cystic Fibrosis Mutations. Genetic Testing. 11(3). 256–268. 5 indexed citations

7.

Milunsky, Jeff M., et al.. (2001). Mutation Analysis in Rett Syndrome. Genetic Testing. 5(4). 321–325. 18 indexed citations

8.

Lebo, Roger V., et al.. (2001). Highly Polymorphic Short Tandem Repeat Analyses Clarify Complex Molecular Test Results. Diagnostic Molecular Pathology. 10(3). 179–189. 1 indexed citations

9.

Sago, Haruhiko, Emily Chen, Victoria Cox, et al.. (1997). True trisomy 2 mosaicism in amniocytes and newborn liver associated with multiple system abnormalities. American Journal of Medical Genetics. 72(3). 343–346. 29 indexed citations

10.

Meuli‐Simmen, Claudia, et al.. (1997). DNA Amplification Determines Donor-Cell Fate in Cryopreserved Skin Allografts. Journal of Reconstructive Microsurgery. 13(7). 497–501. 3 indexed citations

11.

Sago, Haruhiko, et al.. (1997). Dual blastomere analysis improves reliability of preimplantation trembler mouse diagnosis. Human Genetics. 101(2). 223–228. 4 indexed citations

12.

Ravnan, J. Britt, Emily Chen, Mahin Golabi, & Roger V. Lebo. (1996). Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations. American Journal of Medical Genetics. 66(3). 250–256. 38 indexed citations

13.

Lebo, Roger V., et al.. (1994). Ancient, highly polymorphic human major histocompatibility complex DQA1 intron sequences. American Journal of Medical Genetics. 52(4). 438–444. 8 indexed citations

14.

Lebo, Roger V., Lúcia Martelli, Ying Su, et al.. (1993). Prenatal diagnosis of Charcot‐Marie‐Tooth disease type 1a by multicolor in situ hybridization. American Journal of Medical Genetics. 47(3). 441–450. 18 indexed citations

15.

Gruenert, Dieter C., J. Lepercq, Jane Chueh, et al.. (1992). Isolation and characterization of Y chromosome DNA probes. Biochemical and Biophysical Research Communications. 189(1). 581–589. 2 indexed citations

16.

Lebo, Roger V., Richard K. Olney, & Mitchell S. Golbus. (1990). Somatic mosaicism at the duchenne locus. American Journal of Medical Genetics. 37(2). 187–190. 16 indexed citations

17.

Lebo, Roger V.. (1989). Human gene mapping 9: Paris conference (1987). The American Journal of Human Genetics. 44(1). 157–158. 6 indexed citations

18.

Lebo, Roger V., et al.. (1989). Rapid determination of fetal sex by deoxyribonucleic acid amplification of Y chromosome-specific sequences. American Journal of Obstetrics and Gynecology. 161(3). 693–698. 9 indexed citations

19.

Montano, Monty, et al.. (1988). Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes. American Journal of Obstetrics and Gynecology. 158(3). 548–555. 6 indexed citations

20.

Riccardi, Vincent M., Helen Mintz Hittner, Louise C. Strong, et al.. (1982). Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes. The Journal of Pediatrics. 100(4). 574–577. 25 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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