Ryan N. Traylor

1.1k total citations
7 papers, 494 citations indexed

About

Ryan N. Traylor is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ryan N. Traylor has authored 7 papers receiving a total of 494 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Ryan N. Traylor's work include Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Ryan N. Traylor is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Ryan N. Traylor collaborates with scholars based in United States, Australia and Germany. Ryan N. Traylor's co-authors include Jill A. Rosenfeld, Lisa G. Shaffer, Blake C. Ballif, Erawati V. Bawle, Sarah Alliman, Allen N. Lamb, Bassem A. Bejjani, Sangeetha Mahadevan, Richard Person and Trilochan Sahoo and has published in prestigious journals such as PLoS ONE, PEDIATRICS and European Journal of Human Genetics.

In The Last Decade

Ryan N. Traylor

7 papers receiving 473 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ryan N. Traylor United States	7	376	279	115	55	40	7	494
Hiba Risheg United States	10	403 1.1×	374 1.3×	164 1.4×	21 0.4×	53 1.3×	13	640
Marta Smyk Poland	11	373 1.0×	312 1.1×	76 0.7×	29 0.5×	83 2.1×	25	486
Patricia Heard United States	13	391 1.0×	210 0.8×	111 1.0×	25 0.5×	98 2.5×	22	499
Rachel D. Burnside United States	11	460 1.2×	229 0.8×	173 1.5×	23 0.4×	79 2.0×	26	576
Bridgette Soileau United States	11	345 0.9×	165 0.6×	102 0.9×	18 0.3×	71 1.8×	16	408
Carrie Hanscom United States	10	357 0.9×	207 0.7×	132 1.1×	53 1.0×	93 2.3×	10	487
Nicole Maas Belgium	7	351 0.9×	191 0.7×	101 0.9×	21 0.4×	120 3.0×	13	455
Marina Murdolo Italy	13	491 1.3×	383 1.4×	146 1.3×	61 1.1×	171 4.3×	20	663
Anna Maria Nardone Italy	13	213 0.6×	380 1.4×	35 0.3×	33 0.6×	55 1.4×	38	552
Olaya Villa Spain	9	237 0.6×	150 0.5×	126 1.1×	28 0.5×	36 0.9×	17	336

Countries citing papers authored by Ryan N. Traylor

Since Specialization

Citations

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

Fields of papers citing papers by Ryan N. Traylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryan N. Traylor. 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 Ryan N. Traylor. The network helps show where Ryan N. Traylor may publish in the future.

Co-authorship network of co-authors of Ryan N. Traylor

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

All Works

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7 of 7 papers shown

1.

Rosenfeld, Jill A., Ryan N. Traylor, G. Bradley Schaefer, et al.. (2012). Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes. European Journal of Human Genetics. 20(7). 754–761. 82 indexed citations

2.

Traylor, Ryan N., William B. Dobyns, Jill A. Rosenfeld, et al.. (2012). Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions. Molecular Syndromology. 3(3). 102–112. 31 indexed citations

3.

Ellison, Jay W., J. Britt Ravnan, Jill A. Rosenfeld, et al.. (2012). Clinical Utility of Chromosomal Microarray Analysis. PEDIATRICS. 130(5). e1085–e1095. 37 indexed citations

4.

Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2011). The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes. Prenatal Diagnosis. 31(8). 778–787. 33 indexed citations

5.

Duker, Angela L., Blake C. Ballif, Erawati V. Bawle, et al.. (2010). Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome. European Journal of Human Genetics. 18(11). 1196–1201. 236 indexed citations

6.

Traylor, Ryan N., Damien L. Bruno, Trent Burgess, et al.. (2010). A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33. PLoS ONE. 5(8). e12462–e12462. 21 indexed citations

7.

Traylor, Ryan N., Zheng Fan, Jill A. Rosenfeld, et al.. (2009). Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report. Molecular Cytogenetics. 2(1). 17–17. 54 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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