Erin L. Youngs

440 total citations
10 papers, 312 citations indexed

About

Erin L. Youngs is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Erin L. Youngs has authored 10 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Erin L. Youngs's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Congenital heart defects research (2 papers). Erin L. Youngs is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Congenital heart defects research (2 papers). Erin L. Youngs collaborates with scholars based in United States and India. Erin L. Youngs's co-authors include Merlin G. Butler, Jessica A. Hellings, Vikram Jaswaney, Andrew J. Carroll, Janice Smith, James Tepperberg, Fady M. Mikhail, Peter Papenhausen, Inder Gadi and Hiba Risheg and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Erin L. Youngs

10 papers receiving 308 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erin L. Youngs United States	9	261	166	56	53	35	10	312
Laura Conway United States	13	178 0.7×	161 1.0×	33 0.6×	64 1.2×	86 2.5×	25	388
Verayuth Praphanphoj Thailand	12	138 0.5×	181 1.1×	13 0.2×	28 0.5×	35 1.0×	20	328
Lynette Lau Canada	8	189 0.7×	197 1.2×	78 1.4×	70 1.3×	8 0.2×	16	401
Paola Francesca Ajmone Italy	11	149 0.6×	149 0.9×	69 1.2×	27 0.5×	14 0.4×	38	331
She Min Zeng United States	7	229 0.9×	118 0.7×	56 1.0×	48 0.9×	21 0.6×	8	337
Katrin Männik Estonia	7	163 0.6×	124 0.7×	41 0.7×	25 0.5×	25 0.7×	9	222
Federica Zacchini Italy	14	91 0.3×	211 1.3×	15 0.3×	175 3.3×	17 0.5×	26	486
Stanley Walzer United States	8	270 1.0×	145 0.9×	42 0.8×	88 1.7×	27 0.8×	13	387
Barbara Wiśniowiecka‐Kowalnik Poland	8	306 1.2×	214 1.3×	155 2.8×	49 0.9×	71 2.0×	11	445
Stephen C. Collins United States	9	130 0.5×	160 1.0×	52 0.9×	72 1.4×	7 0.2×	12	333

Countries citing papers authored by Erin L. Youngs

Since Specialization

Citations

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

Fields of papers citing papers by Erin L. Youngs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erin L. Youngs. 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 Erin L. Youngs. The network helps show where Erin L. Youngs may publish in the future.

Co-authorship network of co-authors of Erin L. Youngs

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

All Works

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10 of 10 papers shown

Rauscher, Emily A., et al.. (2015). Privacy and Family Communication about Genetic Cancer Risk: Investigating Factors Promoting Women’s Disclosure Decisions. Journal of Family Communication. 15(4). 368–386. 22 indexed citations

Butler, Merlin G., Erin L. Youngs, Jennifer Roberts, & Jessica A. Hellings. (2012). Assessment and Treatment in Autism Spectrum Disorders: A Focus on Genetics and Psychiatry. SHILAP Revista de lepidopterología. 2012. 1–11. 14 indexed citations

Youngs, Erin L., Rebecca S. Henkhaus, Jessica A. Hellings, & Merlin G. Butler. (2011). IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features. European Journal of Medical Genetics. 55(1). 32–36. 24 indexed citations

Youngs, Erin L., Jessica A. Hellings, & Merlin G. Butler. (2011). A clinical report and further delineation of the 14q32 deletion syndrome. Clinical Dysmorphology. 20(3). 143–147. 10 indexed citations

Burnside, Rachel D., Romela Pasion, Inder Gadi, et al.. (2011). Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay Rachel D. BurnsideRomela PasionFady M. MikhailAndrew J. CarrollNathaniel H. Robin • Erin L. YoungsInder K. GadiElizabeth KeitgesVikram L. JaswaneyPeter R. Papenhausen • Venkateswara R. PotluriHiba RishegBrooke RushJanice L. SmithStuart Schwartz •. 3 indexed citations

Burnside, Rachel D., Romela Pasion, Fady M. Mikhail, et al.. (2011). Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Human Genetics. 130(4). 517–528. 182 indexed citations

Youngs, Erin L., Jessica A. Hellings, & Merlin G. Butler. (2011). ANKRD11 gene deletion in a 17-year-old male. Clinical Dysmorphology. 20(3). 170–171. 21 indexed citations

Youngs, Erin L., Rebecca S. Henkhaus, Jessica A. Hellings, & Merlin G. Butler. (2011). 12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes. Clinical Dysmorphology. 21(2). 93–96. 10 indexed citations

Dasouki, Majed, Erin L. Youngs, & Karine Hovanes. (2011). Structural Chromosome Abnormalities Associated with Obesity: Report of Four New Subjects and Review of Literature. Current Genomics. 12(3). 190–203. 16 indexed citations

10.

Youngs, Erin L., et al.. (2009). An 18‐year follow‐up report on an infant with a duplication of 9q34. American Journal of Medical Genetics Part A. 152A(1). 230–233. 10 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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