Emily A. Rorem

1.2k total citations
9 papers, 774 citations indexed

About

Emily A. Rorem is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Emily A. Rorem has authored 9 papers receiving a total of 774 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Plant Science. Recurrent topics in Emily A. Rorem's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (6 papers). Emily A. Rorem is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (6 papers). Emily A. Rorem collaborates with scholars based in United States and Canada. Emily A. Rorem's co-authors include Lisa G. Shaffer, Bassem A. Bejjani, Blake C. Ballif, Kyle Sundin, Catherine D. Kashork, Reza Saleki, Aaron Theisen, Justine Coppinger, Sabrina Craigo and Louise Wilkins‐Haug and has published in prestigious journals such as The Journal of Pediatrics, Genetics in Medicine and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

Emily A. Rorem

9 papers receiving 740 citations

Peers

Emily A. Rorem

GENET

PPCH

MB

PS

SURGE

Angelo Selicorni Italy

Roberta Santos Guilherme Brazil

Morag N. Collinson United Kingdom

Roberto Coco Argentina

N. M. Lawrie United Kingdom

Rachel D. Burnside United States

Sigrid Sahlén Sweden

Viv Maloney United Kingdom

Beth A. Torchia United States

D R Romain New Zealand

Angelo Selicorni Italy

Emily A. Rorem

474 ×0.7

GENET

161 ×0.4

PPCH

322 ×1.2

MB

221 ×1.0

PS

28 ×1.0

SURGE

Citations per year, relative to Emily A. Rorem Emily A. Rorem (= 1×) peers Angelo Selicorni

Countries citing papers authored by Emily A. Rorem

Since Specialization

Citations

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

Fields of papers citing papers by Emily A. Rorem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emily A. Rorem. 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 Emily A. Rorem. The network helps show where Emily A. Rorem may publish in the future.

Co-authorship network of co-authors of Emily A. Rorem

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

All Works

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9 of 9 papers shown

1.

Bianchi, Diana W., Lisa G. Shaffer, Emily A. Rorem, et al.. (2009). Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype. Prenatal Diagnosis. 29(13). 1213–1217. 84 indexed citations

2.

Shevell, Michael, Bassem A. Bejjani, Myriam Srour, et al.. (2008). Array comparative genomic hybridization in global developmental delay. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1101–1108. 36 indexed citations

3.

Shaffer, Lisa G., Blake C. Ballif, Aaron Theisen, et al.. (2008). In the middle of it all: a centered approach to chromosome analysis. Expert Opinion on Medical Diagnostics. 2(2). 221–229. 2 indexed citations

4.

Srour, Myriam, et al.. (2008). An Instructive Case of an 8-Year-Old Boy With Intellectual Disability. Seminars in Pediatric Neurology. 15(4). 154–155. 10 indexed citations

5.

Ballif, Blake C., et al.. (2007). Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH. Genetics in Medicine. 9(3). 150–162. 46 indexed citations

6.

Shaffer, Lisa G., Catherine D. Kashork, Reza Saleki, et al.. (2006). Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases. The Journal of Pediatrics. 149(1). 98–102.e5. 165 indexed citations

7.

Ballif, Blake C., Catherine D. Kashork, Reza Saleki, et al.. (2006). Detecting sex chromosome anomalies and common triploidies in products of conception by array‐based comparative genomic hybridization. Prenatal Diagnosis. 26(4). 333–339. 48 indexed citations

8.

Ballif, Blake C., Emily A. Rorem, Kyle Sundin, et al.. (2006). Detection of low‐level mosaicism by array CGH in routine diagnostic specimens. American Journal of Medical Genetics Part A. 140A(24). 2757–2767. 228 indexed citations

9.

Bejjani, Bassem A., Reza Saleki, Blake C. Ballif, et al.. (2005). Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?. American Journal of Medical Genetics Part A. 134A(3). 259–267. 155 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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