Erin E. Baldwin

657 total citations
15 papers, 383 citations indexed

About

Erin E. Baldwin is a scholar working on Molecular Biology, Developmental and Educational Psychology and Genetics. According to data from OpenAlex, Erin E. Baldwin has authored 15 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Developmental and Educational Psychology and 3 papers in Genetics. Recurrent topics in Erin E. Baldwin's work include Hearing Impairment and Communication (4 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Neurological diseases and metabolism (2 papers). Erin E. Baldwin is often cited by papers focused on Hearing Impairment and Communication (4 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Neurological diseases and metabolism (2 papers). Erin E. Baldwin collaborates with scholars based in United States and Japan. Erin E. Baldwin's co-authors include Richard G. Boles, Patti Krautscheid, Christine E. Miller, Danielle LaGrave, Kim Hart, Tatiana Tvrdik, Christina G.S. Palmer, Patrick Boudreault, Janet S. Sinsheimer and Tomoyasu Higashimoto and has published in prestigious journals such as PLoS ONE, Hepatology and Archives of Disease in Childhood.

In The Last Decade

Erin E. Baldwin

14 papers receiving 373 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erin E. Baldwin United States	10	135	127	74	57	44	15	383
Yong‐Hui Jiang United States	11	155 1.1×	194 1.5×	22 0.3×	43 0.8×	48 1.1×	12	444
Ricardo Godinho Brazil	7	153 1.1×	41 0.3×	67 0.9×	6 0.1×	47 1.1×	21	375
Jao‐Shwann Liang Taiwan	13	159 1.2×	177 1.4×	36 0.5×	72 1.3×	31 0.7×	44	458
Katherine Christensen United States	10	61 0.5×	98 0.8×	18 0.2×	62 1.1×	122 2.8×	21	339
Heidi Mateus Colombia	11	165 1.2×	119 0.9×	10 0.1×	31 0.5×	30 0.7×	32	362
Joseph D. Symonds United Kingdom	12	206 1.5×	282 2.2×	51 0.7×	144 2.5×	36 0.8×	30	711
Nadia Ali United States	11	50 0.4×	60 0.5×	31 0.4×	47 0.8×	169 3.8×	73	433
R. Kálmánchey Hungary	10	206 1.5×	80 0.6×	105 1.4×	85 1.5×	25 0.6×	27	422
Sandra Sabbagh Lebanon	11	118 0.9×	68 0.5×	84 1.1×	153 2.7×	39 0.9×	30	369
K Stephens United States	7	79 0.6×	52 0.4×	15 0.2×	27 0.5×	37 0.8×	133	296

Countries citing papers authored by Erin E. Baldwin

Since Specialization

Citations

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

Fields of papers citing papers by Erin E. Baldwin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erin E. Baldwin

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

All Works

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15 of 15 papers shown

Wen, Ting, Steven E. Boyden, Robert G. Lewis, et al.. (2025). Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing. Blood Advances. 9(10). 2443–2452.

Herriges, John, et al.. (2018). Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature. Journal of Child Neurology. 34(2). 86–93. 1 indexed citations

Miller, Christine E., Patti Krautscheid, Erin E. Baldwin, et al.. (2014). Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing. American Journal of Medical Genetics Part A. 164(5). 1094–1101. 98 indexed citations

Andersen, Erica, Erin E. Baldwin, Sara Ellingwood, Rosemarie Smith, & Allen N. Lamb. (2014). Xq28 duplication overlapping the int22h‐1/int22h‐2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability. American Journal of Medical Genetics Part A. 164(7). 1795–1801. 31 indexed citations

Palmer, Christina G.S., Patrick Boudreault, Erin E. Baldwin, & Janet S. Sinsheimer. (2014). Impact of Genetic Counseling and Connexin-26 and Connexin-30 Testing on Deaf Identity and Comprehension of Genetic Test Results in a Sample of Deaf Adults: A Prospective, Longitudinal Study. PLoS ONE. 9(11). e111512–e111512. 9 indexed citations

Vanzo, Rena, Megan Martin, Erin E. Baldwin, et al.. (2014). Clinical Utility of Chromosomal Microarray Analysis of DNA from Buccal Cells: Detection of Mosaicism in Three Patients. Journal of Genetic Counseling. 23(6). 922–927. 13 indexed citations

Baldwin, Erin E., et al.. (2014). L1CAM whole gene deletion in a child with L1 syndrome. American Journal of Medical Genetics Part A. 164(6). 1555–1558. 8 indexed citations

Palmer, Christina G.S., Patrick Boudreault, Erin E. Baldwin, et al.. (2013). Deaf Genetic Testing and Psychological Well‐Being in Deaf Adults. Journal of Genetic Counseling. 22(4). 492–507. 14 indexed citations

Baldwin, Erin E., Patrick Boudreault, Michelle Fox, Janet S. Sinsheimer, & Christina G.S. Palmer. (2011). Effect of Pre‐test Genetic Counseling for Deaf Adults on Knowledge of Genetic Testing. Journal of Genetic Counseling. 21(2). 256–272. 18 indexed citations

10.

Chang, Vivian Y., Fabiola Quintero‐Rivera, Erin E. Baldwin, et al.. (2010). B‐Acute lymphoblastic leukemia and cystinuria in a patient with duplication 22q11.21 detected by chromosomal microarray analysis. Pediatric Blood & Cancer. 56(3). 470–473. 7 indexed citations

11.

Boudreault, Patrick, Erin E. Baldwin, Michelle Fox, et al.. (2010). Deaf Adults' Reasons for Genetic Testing Depend on Cultural Affiliation: Results From a Prospective, Longitudinal Genetic Counseling and Testing Study. The Journal of Deaf Studies and Deaf Education. 15(3). 209–227. 30 indexed citations

12.

Rosser, Tena, et al.. (2010). Transient Leukoencephalopathy Associated With X-Linked Charcot-Marie-Tooth Disease. Journal of Child Neurology. 25(8). 1013–1016. 16 indexed citations

13.

Higashimoto, Tomoyasu, Erin E. Baldwin, Jeffrey I. Gold, & Richard G. Boles. (2008). Reflex sympathetic dystrophy: complex regional pain syndrome type I in children with mitochondrial disease and maternal inheritance. Archives of Disease in Childhood. 93(5). 390–397. 33 indexed citations

14.

Wong, Lee-Jun, Nicola Brunetti‐Pierri, Qing Zhang, et al.. (2007). Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy. Hepatology. 46(4). 1218–1227. 94 indexed citations

15.

Boles, Richard G., Erin E. Baldwin, & Toni R. Prezant. (2007). Combined Cyclic Vomiting and Kearns-Sayre Syndromes. Pediatric Neurology. 36(2). 135–136. 11 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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