Lawrence M. Silverman

5.2k total citations · 1 hit paper
97 papers, 3.6k citations indexed

About

Lawrence M. Silverman is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Lawrence M. Silverman has authored 97 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Pulmonary and Respiratory Medicine, 34 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Lawrence M. Silverman's work include Cystic Fibrosis Research Advances (25 papers), Neonatal Respiratory Health Research (9 papers) and Muscle Physiology and Disorders (8 papers). Lawrence M. Silverman is often cited by papers focused on Cystic Fibrosis Research Advances (25 papers), Neonatal Respiratory Health Research (9 papers) and Muscle Physiology and Disorders (8 papers). Lawrence M. Silverman collaborates with scholars based in United States, France and Ireland. Lawrence M. Silverman's co-authors include Kenneth J. Friedman, Michael R. Knowles, Jonathan Cohn, Peadar G. Noone, Paul S. Jowell, Zhaoqing Zhou, Arthur J. Siegel, W. Edward Highsmith, Elizabeth M. Rohlfs and Nader Rifai and has published in prestigious journals such as New England Journal of Medicine, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Lawrence M. Silverman

93 papers receiving 3.5k 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.

Relation between Mutations of the Cystic Fibrosis Gene and Idiopathic Pancreatitis

1998 622 citations Jonathan Cohn, Kenneth J. Friedman et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lawrence M. Silverman United States	28	1.2k	917	894	586	494	97	3.6k
Manuel R. Gómez United States	44	865 0.7×	1.5k 1.6×	630 0.7×	835 1.4×	803 1.6×	116	6.5k
Shiro Saito Japan	32	986 0.8×	991 1.1×	671 0.8×	562 1.0×	181 0.4×	261	3.8k
Peter S. Amenta United States	34	631 0.5×	1.5k 1.7×	982 1.1×	638 1.1×	566 1.1×	115	5.0k
Hitoo Nakano Japan	38	613 0.5×	1.0k 1.1×	722 0.8×	882 1.5×	244 0.5×	205	4.6k
Laurent Daniel France	34	1.1k 0.9×	1.5k 1.7×	645 0.7×	396 0.7×	234 0.5×	161	4.1k
Hirohiko Yamabe Japan	34	637 0.5×	602 0.7×	906 1.0×	832 1.4×	155 0.3×	105	3.6k
Rodney D. McComb United States	37	391 0.3×	1.3k 1.4×	492 0.6×	449 0.8×	433 0.9×	112	4.1k
Enric Condom Spain	37	636 0.5×	1.7k 1.8×	919 1.0×	533 0.9×	241 0.5×	106	3.6k
James S. Hagood United States	43	2.8k 2.4×	1.9k 2.1×	918 1.0×	726 1.2×	249 0.5×	101	5.7k
Carl Atkinson United States	38	1.6k 1.4×	1.1k 1.2×	1.1k 1.2×	433 0.7×	174 0.4×	141	4.9k

Countries citing papers authored by Lawrence M. Silverman

Since Specialization

Citations

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

Fields of papers citing papers by Lawrence M. Silverman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lawrence M. Silverman

This figure shows the co-authorship network connecting the top 25 collaborators of Lawrence M. Silverman. A scholar is included among the top collaborators of Lawrence M. Silverman 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 Lawrence M. Silverman. Lawrence M. Silverman 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

Silverman, Lawrence M., et al.. (2014). Chronotropic Incompetence Precedes Silent Pulmonary Embolism. Current Sports Medicine Reports. 13(2). 72–74.

Tsongalis, Gregory J. & Lawrence M. Silverman. (2006). Molecular diagnostics: A historical perspective. Clinica Chimica Acta. 369(2). 188–192. 12 indexed citations

Sugarman, Elaine A., Elizabeth M. Rohlfs, Lawrence M. Silverman, & Bernice A. Allitto. (2004). CFTR mutation distribution among U.S. Hispanic and African American individuals: Evaluation in cystic fibrosis patient and carrier screening populations. Genetics in Medicine. 6(5). 392–399. 57 indexed citations

Shaheen, Nicholas J., Lawrence M. Silverman, Temitope O. Keku, et al.. (2003). Association Between Hemochromatosis (HFE) Gene Mutation Carrier Status and the Risk of Colon Cancer. JNCI Journal of the National Cancer Institute. 95(2). 154–159. 92 indexed citations

Rohlfs, Elizabeth M., Zhaoqing Zhou, Elaine A. Sugarman, et al.. (2002). The I148T CFTR allele occurs on multiple haplotypes: A complex allele is associated with cystic fibrosis. Genetics in Medicine. 4(5). 319–323. 56 indexed citations

Noone, Peadar G., Zhaoqing Zhou, Emma Wakeling, et al.. (2000). Lung Disease Associated with the IVS8 5T Allele of the CFTR Gene. American Journal of Respiratory and Critical Care Medicine. 162(5). 1919–1924. 76 indexed citations

Rohlfs, Elizabeth M., Nadine Puget, Mark L. Graham, et al.. (2000). AnAlu-mediated 7.1 kb deletion ofBRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10. Genes Chromosomes and Cancer. 28(3). 300–307. 60 indexed citations

Rohlfs, Elizabeth M., Christine H. Chung, Qing Yang, et al.. (2000). In-frame deletions of BRCA1 may define critical functional domains. Human Genetics. 107(4). 385–390. 24 indexed citations

Friedman, Kenneth J., Jolanta Kole, Jonathan Cohn, et al.. (1999). Correction of Aberrant Splicing of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene by Antisense Oligonucleotides. Journal of Biological Chemistry. 274(51). 36193–36199. 116 indexed citations

10.

Rohlfs, Elizabeth M., et al.. (1998). Is the Hemochromatosis Gene a Modifier Locus for Cystic Fibrosis?. Genetic Testing. 2(1). 85–88. 22 indexed citations

11.

Cohn, Jonathan, Kenneth J. Friedman, Peadar G. Noone, et al.. (1998). Relation between Mutations of the Cystic Fibrosis Gene and Idiopathic Pancreatitis. New England Journal of Medicine. 339(10). 653–658. 622 indexed citations breakdown →

12.

Friedman, Kenneth J., Ruth A. Heim, Michael R. Knowles, & Lawrence M. Silverman. (1997). Rapid characterization of the variable length polythymidine tract in the cystic fibrosis (CFTR) gene: Association of the 5T allele with selected CFTR mutations and its incidence in atypical sinopulmonary disease. Human Mutation. 10(2). 108–115. 67 indexed citations

13.

Highsmith, W. Edward, Lauranell H. Burch, Zhaoqing Zhou, et al.. (1997). Identification of a splice site mutation (2789+5 G>A) associated with small amounts of normal CFTRmRNA and mild cystic fibrosis. Human Mutation. 9(4). 332–338. 61 indexed citations

14.

Friedman, Kenneth J., Harry Teichtahl, David M. de Kretser, et al.. (1995). Screening Young Syndrome Patients for CFTR Mutations. American Journal of Respiratory and Critical Care Medicine. 152(4). 1353–1357. 17 indexed citations

15.

Heim, Ruth A., Lauren Kam-Morgan, Cameron G. Binnie, et al.. (1995). Distribution of 13 truncating mutations in the neurofibromatosis 1 gene. Human Molecular Genetics. 4(6). 975–981. 144 indexed citations

16.

Highsmith, W. Edward, Lauranell H. Burch, Zhaoqing Zhou, et al.. (1994). A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations. New England Journal of Medicine. 331(15). 974–980. 339 indexed citations

17.

Silverman, Lawrence M., et al.. (1993). Effect of melanin, oxyhemoglobin and bilirubin on transcutaneous bilirubinometry. Acta Paediatrica. 82(1). 19–21. 26 indexed citations

18.

Prior, Thomas W., Kenneth J. Friedman, & Lawrence M. Silverman. (1989). RFLP for HindIII at the Duchenne muscular dystrophy gene. Nucleic Acids Research. 17(6). 2370–2370. 4 indexed citations

19.

Bankson, Daniel D., Nader Rifai, Mary Elizabeth Williams, Lawrence M. Silverman, & T K Gray. (1989). Biochemical effects of 17β-estradiol on UMR106 cells. Bone and Mineral. 6(1). 55–63. 26 indexed citations

20.

LeGrys, Vicky A., et al.. (1987). Clinical Applications of DNA Probes in the Diagnosis of Genetic Diseases. CRC Critical Reviews in Clinical Laboratory Sciences. 25(4). 255–274. 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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