Steven Schonberg

704 total citations
19 papers, 422 citations indexed

About

Steven Schonberg is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Steven Schonberg has authored 19 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Steven Schonberg's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Steven Schonberg is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Steven Schonberg collaborates with scholars based in United States and Canada. Steven Schonberg's co-authors include James German, Joanna Groden, Kelly A. Combs, Gregory K. Behbehani, John J. Turchi, David K. Orren, Amrita Machwe, Mahin Golabi, Charles M. Strom and Trilochan Sahoo and has published in prestigious journals such as Nature, Blood and Human Molecular Genetics.

In The Last Decade

Steven Schonberg

18 papers receiving 404 citations

Peers

Steven Schonberg

GENET

PPCH

PHYSI

Gabriella E. Martyn Australia

R Elles United Kingdom

Shane C. Quinonez United States

Bogdan Kałużewski Poland

Barbara Delle Chiaie Belgium

Pingyuan Xie China

Ko–ichiro Yoshiura Japan

Satya K. Kota France

Shun‐Ping Chang Taiwan

Berta Santesson Sweden

Gabriella E. Martyn Australia

Steven Schonberg

548 ×2.2

102 ×0.7

GENET

185 ×1.7

PPCH

78 ×1.0

PHYSI

39 ×0.8

Citations per year, relative to Steven Schonberg Steven Schonberg (= 1×) peers Gabriella E. Martyn

Countries citing papers authored by Steven Schonberg

Since Specialization

Citations

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

Fields of papers citing papers by Steven Schonberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven Schonberg

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

All Works

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19 of 19 papers shown

Chandrasekhar, Anjana, Nora Urraca, Andrew M. Gross, et al.. (2023). Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes. American Journal of Medical Genetics Part A. 194(3). e63462–e63462. 2 indexed citations

Wang, Jia‐Chi, et al.. (2015). Discordant Noninvasive Prenatal Testing and Cytogenetic Results. Obstetrical & Gynecological Survey. 70(7). 434–436. 2 indexed citations

Wang, Jia‐Chi, et al.. (2014). Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases. Genetics in Medicine. 17(3). 234–236. 65 indexed citations

Dai, Zunyan, JoAnn C. Kelly, Aurelia Meloni‐Ehrig, et al.. (2012). Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas. Molecular Cytogenetics. 5(1). 44–44. 26 indexed citations

Meloni‐Ehrig, Aurelia, Jeanne Meck, JoAnn C. Kelly, et al.. (2009). Stimulation of B-Cell Mature Malignancies with the CpG-Oligonucleotide DSP30 and Interleukin-2 for Improved Detection of Chromosome Abnormalities.. Blood. 114(22). 1955–1955. 1 indexed citations

Gallivan, Monica V.E., Robin Hanson, Steven Schonberg, et al.. (2005). Hemoglobin H Hydrops Fetalis Associated with Homozygous Hemoglobin Constant Spring. Case Report.. Blood. 106(11). 3821–3821.

Machwe, Amrita, Kelly A. Combs, Gregory K. Behbehani, et al.. (2004). Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2. Human Molecular Genetics. 13(17). 1919–1932. 132 indexed citations

Fries, Melissa H., Roger V. Lebo, Steven Schonberg, et al.. (1993). Mental retardation locus in Xp21 chromosome microdeletion. American Journal of Medical Genetics. 46(4). 363–368. 23 indexed citations

Cox, Victoria, et al.. (1992). Pallister‐Hall syndrome associated with an unbalanced chromosome translocation. American Journal of Medical Genetics. 43(3). 647–650. 25 indexed citations

10.

Kratzer, Paul G., M S Golbus, Steven Schonberg, David C. Heilbron, & Robert N. Taylor. (1992). Cytogenetic evidence for enhanced selective miscarriage of trisomy 21 pregnancies with advancing maternal age. American Journal of Medical Genetics. 44(5). 657–663. 16 indexed citations

11.

Jenkins, Edmund C., W. Ted Brown, Steven Schonberg, et al.. (1992). Prenatal detection of Fra(X)(q27.3) in female identical twins: Reliability of low level cytogenetic prenatal expression in females. American Journal of Medical Genetics. 43(1-2). 128–135. 4 indexed citations

12.

Jenkins, Lauren S., Dieter C. Gruenert, Edmund C. Jenkins, & Steven Schonberg. (1991). Transformation and establishment of fragile X cell lines from amniocytes. American Journal of Medical Genetics. 38(2-3). 416–417. 2 indexed citations

13.

Jenkins, Edmund C., W. Ted Brown, Michael S. Krawczun, et al.. (1988). Recent experience in prenatal fra(X) detection. American Journal of Medical Genetics. 30(1-2). 329–336. 15 indexed citations

14.

Johnston, Kathreen, Steven Schonberg, Teresa Gregory, et al.. (1987). De novo X;Y translocation associated with imperforate anus and retinal pigmentary abnormalities. American Journal of Medical Genetics. 27(3). 603–611. 14 indexed citations

15.

Hogge, Donna E., Kevin Shannon, Dagmar K. Kalousek, et al.. (1987). Juvenile monosomy 7 syndrome: evidence that the disease originates in a pluripotent hemopoietic stem cell. Leukemia Research. 11(8). 705–709. 21 indexed citations

16.

Holzgreve, Wolfgang, et al.. (1985). X-Chromosome Hyperploidy in Couples with Multiple Spontaneous Abortions. Obstetrical & Gynecological Survey. 40(4). 247–247. 17 indexed citations

17.

Epstein, Charles J., David R. Cox, Steven Schonberg, & W. Allen Hogge. (1983). RECENT DEVELOPMENTS IN THE PRENATAL DIAGNOSIS OF GENETIC DISEASES AND BIRTH DEFECTS. Annual Review of Genetics. 17(1). 49–83. 15 indexed citations

18.

Schonberg, Steven, David Patterson, & Theodore T. Puck. (1983). Resistance of chinese hamster ovary cell chromatin to endonuclease digestion. Experimental Cell Research. 145(1). 57–62. 19 indexed citations

19.

Schonberg, Steven & James German. (1980). Sister chromatid exchange in cells metabolically coupled to Bloom's syndrome cells. Nature. 284(5751). 72–74. 23 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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