Frank Greenberg

10.2k total citations · 2 hit papers
112 papers, 7.2k citations indexed

About

Frank Greenberg is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Frank Greenberg has authored 112 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 41 papers in Molecular Biology and 34 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Frank Greenberg's work include Prenatal Screening and Diagnostics (29 papers), Genomic variations and chromosomal abnormalities (24 papers) and Genetic Syndromes and Imprinting (15 papers). Frank Greenberg is often cited by papers focused on Prenatal Screening and Diagnostics (29 papers), Genomic variations and chromosomal abnormalities (24 papers) and Genetic Syndromes and Imprinting (15 papers). Frank Greenberg collaborates with scholars based in United States, United Kingdom and Italy. Frank Greenberg's co-authors include David H. Ledbetter, Merlin G. Butler, William B. Dobyns, Suzanne B. Cassidy, Vanja A. Holm, Louise R. Greenswag, Jeanne M. Hanchett, Barbara Y. Whitman, James F. Reynolds and Lisa G. Shaffer and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Gastroenterology.

In The Last Decade

Frank Greenberg

108 papers receiving 6.9k 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.

Prader-Willi Syndrome: Consensus Diagnostic Criteria

1993 929 citations Frank Greenberg et al. profile →
Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder

1999 504 citations Frank Greenberg et al. profile →

Peers

Frank Greenberg

GENET

MB

PPCH

SURGE

GENET

Dian Donnai United Kingdom

Ben C.J. Hamel Netherlands

Jean‐Pierre Fryns Belgium

Alain Verloès France

William Reardon United Kingdom

Outi Hovatta Sweden

Orsetta Zuffardi Italy

Michel Vekemans France

Anita Rauch Germany

Eric Legius Belgium

Dian Donnai United Kingdom

Frank Greenberg

3.0k ×0.8

GENET

3.1k ×1.0

MB

1.2k ×0.9

PPCH

1.1k ×1.2

SURGE

418 ×0.5

GENET

Citations per year, relative to Frank Greenberg Frank Greenberg (= 1×) peers Dian Donnai

Countries citing papers authored by Frank Greenberg

Since Specialization

Citations

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

Fields of papers citing papers by Frank Greenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Frank Greenberg. 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 Frank Greenberg. The network helps show where Frank Greenberg may publish in the future.

Co-authorship network of co-authors of Frank Greenberg

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

Greenberg, Frank, et al.. (2005). Williams syndrome in twins. American Journal of Medical Genetics. 37(S6). 97–99. 6 indexed citations

2.

Smith, Ann C. M., Elizabeth Dykens, & Frank Greenberg. (1998). Behavioral phenotype of smith-magenis syndrome (del 17p11.2). American Journal of Medical Genetics. 81(2). 179–185. 115 indexed citations

3.

McCaskill, Christopher, et al.. (1996). A clinical and molecular study of mosaicism for trisomy 17. Human Genetics. 97(1). 69–72. 33 indexed citations

4.

Canfield, Mark A., J. F. Annegers, Jean D. Brender, S. P. Cooper, & Frank Greenberg. (1996). Hispanic Origin and Neural Tube Defects in Houston/Harris County, Texas: I. Descriptive Epidemiology. American Journal of Epidemiology. 143(1). 1–11. 57 indexed citations

5.

Lupski, James R., et al.. (1996). Ophthalmic Manifestations of Smith-Magenis Syndrome. Ophthalmology. 103(7). 1084–1091. 30 indexed citations

6.

Greenberg, Frank, Richard A. Lewis, Lorraine Potocki, et al.. (1996). Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2). American Journal of Medical Genetics. 62(3). 247–254. 239 indexed citations

7.

Kobayashi, Hitome, L. Baumbach, Tara C. Matise, et al.. (1995). A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2. Human Molecular Genetics. 4(7). 1213–1216. 54 indexed citations

8.

Juyal, Ramesh C., Frank Greenberg, James R. Lupski, et al.. (1995). Smith‐Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization. American Journal of Medical Genetics. 58(3). 286–291. 22 indexed citations

9.

Greenberg, Frank, et al.. (1994). Deletions of the elastin gene in Williams Syndrome. The American Journal of Human Genetics. 55. 2 indexed citations

10.

Shaffer, Lisa G., et al.. (1994). Very low maternal serum chorionic gonadotropin levels in association with fetal triploidy. American Journal of Obstetrics and Gynecology. 170(1). 77–80.

11.

Greenberg, Frank. (1993). DiGeorge syndrome: an historical review of clinical and cytogenetic features.. Journal of Medical Genetics. 30(10). 803–806. 64 indexed citations

12.

Greenberg, Frank, et al.. (1992). Congenital deficiency of α-fetoprotein. American Journal of Obstetrics and Gynecology. 167(2). 509–511. 11 indexed citations

13.

Wagstaff, John, Joan H.M. Knoll, J Fleming, et al.. (1991). Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.. PubMed. 49(2). 330–7. 155 indexed citations

14.

Greenberg, Frank, et al.. (1991). The effect of gestational age on the detection rate of Down's syndrome by maternal serum α-fetoprotein screening. American Journal of Obstetrics and Gynecology. 165(5). 1391–1393. 3 indexed citations

15.

Greenberg, Frank, et al.. (1991). Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. Human Genetics. 87(4). 452–6. 30 indexed citations

16.

Greenberg, Frank, et al.. (1990). Hereditary persistence of alpha-fetoprotein. Gastroenterology. 98(4). 1083–1085. 26 indexed citations

17.

Greenberg, Frank, Warren W. Wasiewski, & Edward R.B. McCabe. (1989). Weaver syndrome: The changing phenotype in an adult. American Journal of Medical Genetics. 33(1). 127–129. 13 indexed citations

18.

Greenberg, Frank, et al.. (1988). 1987 ASHG workshop: Low maternal serum AFP screening for down syndrome. American Journal of Medical Genetics. 31(1). 193–196. 1 indexed citations

19.

Gollin, Susanne M., Frank Greenberg, Vincent M. Riccardi, et al.. (1987). Duplication of proximal 15q as a cause of Prader‐Willi syndrome. American Journal of Medical Genetics. 28(4). 791–802. 36 indexed citations

20.

Greenberg, Frank, Cecilia T. Valdés, Howard M. Rosenblatt, John L. Kirkland, & David H. Ledbetter. (1986). Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome. The Journal of Pediatrics. 109(3). 489–492. 31 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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