Joy Samanich

585 total citations
17 papers, 289 citations indexed

About

Joy Samanich is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Joy Samanich has authored 17 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Sensory Systems. Recurrent topics in Joy Samanich's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), Congenital heart defects research (4 papers) and Connexins and lens biology (3 papers). Joy Samanich is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), Congenital heart defects research (4 papers) and Connexins and lens biology (3 papers). Joy Samanich collaborates with scholars based in United States, United Kingdom and New Zealand. Joy Samanich's co-authors include Bernice E. Morrow, Alan Shanske, Melanie Babcock, Robert D. Burk, Christina Lowes, Sara Shanske, Deepa Manwani, Saima Riazuddin, Gregory I. Frolenkov and Payal Patel and has published in prestigious journals such as PLoS ONE, Gene and Clinical Genetics.

In The Last Decade

Joy Samanich

17 papers receiving 284 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joy Samanich United States 10 141 88 86 34 30 17 289
Nabil Driss Tunisia 8 123 0.9× 51 0.6× 142 1.7× 70 2.1× 25 0.8× 25 298
Angelien Heister Netherlands 10 227 1.6× 69 0.8× 84 1.0× 61 1.8× 10 0.3× 10 437
Joon Suk Lee South Korea 10 123 0.9× 67 0.8× 80 0.9× 32 0.9× 17 0.6× 14 284
Mariem Ben Saïd Tunisia 11 174 1.2× 95 1.1× 214 2.5× 101 3.0× 21 0.7× 26 369
Alisha Wilkens United States 13 239 1.7× 255 2.9× 61 0.7× 25 0.7× 34 1.1× 20 438
Jiale Xiang China 9 172 1.2× 88 1.0× 85 1.0× 23 0.7× 10 0.3× 24 345
Ανδρέας Παμπάνος Greece 12 233 1.7× 140 1.6× 186 2.2× 76 2.2× 16 0.5× 28 459
Catherine Bromhead Australia 8 169 1.2× 150 1.7× 37 0.4× 29 0.9× 36 1.2× 8 287
Chufeng He China 14 286 2.0× 73 0.8× 172 2.0× 59 1.7× 40 1.3× 52 447
Isabella Rau Germany 6 138 1.0× 97 1.1× 43 0.5× 18 0.5× 12 0.4× 9 236

Countries citing papers authored by Joy Samanich

Since Specialization
Citations

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

Fields of papers citing papers by Joy Samanich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joy Samanich

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

All Works

17 of 17 papers shown
1.
Giese, Arnaud P. J., Joy Samanich, Saima Riazuddin, et al.. (2015). A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family. PLoS ONE. 10(10). e0133082–e0133082. 60 indexed citations
2.
Samanich, Joy, Cristina Montagna, Melanie Babcock, & Bernice E. Morrow. (2015). Interstitial duplication of 22q13.2 in a girl with short stature, impaired speech and language, and dysmorphism. Journal of Pediatric Genetics. 1(1). 47–53. 5 indexed citations
3.
Ma, Deqiong, Robert Marion, Elaine M. Pereira, et al.. (2014). A de novo 10.79 Mb interstitial deletion at 2q13q14.2 involving PAX8 causing hypothyroidism and mullerian agenesis: a novel case report and literature review. Molecular Cytogenetics. 7(1). 85–85. 21 indexed citations
4.
Wang, Tao, Joy Samanich, Chad Haldeman‐Englert, et al.. (2013). Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams–Beuren syndrome. American Journal of Medical Genetics Part A. 161(3). 527–533. 19 indexed citations
5.
Robertson, Stephen P., et al.. (2013). Severe osteopathia striata with cranial sclerosis in a female case with whole WTX gene deletion. American Journal of Medical Genetics Part A. 161(3). 594–599. 10 indexed citations
6.
7.
Samanich, Joy, et al.. (2012). 17q12 Deletion in a patient with Williams syndrome: Case report and review of the literature.. PubMed. 1(2). 135–41. 2 indexed citations
8.
Morgan, Tim, Geneviève Baujat, Valérie Cormier‐Daire, et al.. (2012). Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locus. Clinical Genetics. 83(3). 251–256. 20 indexed citations
9.
Samanich, Joy, Qiulu Pan, Chih-Kang Huang, et al.. (2011). Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature. American Journal of Medical Genetics Part A. 155(4). 825–832. 8 indexed citations
10.
Patel, Payal, Joy Samanich, W. Beau Mitchell, & Deepa Manwani. (2011). A unique presentation of Wiskott–Aldrich syndrome in relation to platelet size. Pediatric Blood & Cancer. 56(7). 1127–1129. 18 indexed citations
11.
Morrow, Bernice E., et al.. (2011). Agnathia–otocephaly complex: A case report and examination of the OTX2 and PRRX1 genes. Gene. 494(1). 124–129. 18 indexed citations
12.
Jahangir, Arthee, et al.. (2010). Mutational analysis of HOXA2 and SIX2 in a Bronx population with isolated microtia. International Journal of Pediatric Otorhinolaryngology. 74(8). 878–882. 22 indexed citations
13.
Shan, Jidong, Raquel Castellanos, Melanie Babcock, et al.. (2010). GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent. International Journal of Pediatric Otorhinolaryngology. 74(6). 611–618. 19 indexed citations
14.
Samanich, Joy, et al.. (2009). Cleft Palate. Pediatrics in Review. 30(6). 230–232. 5 indexed citations
15.
Samanich, Joy. (2009). Cleft Palate. Pediatrics in Review. 30(6). 230–232. 2 indexed citations
16.
Samanich, Joy, et al.. (2008). Genetic evaluation of American minority pediatric cochlear implant recipients. International Journal of Pediatric Otorhinolaryngology. 73(2). 195–203. 6 indexed citations
17.
Samanich, Joy, Christina Lowes, Robert D. Burk, et al.. (2007). Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment. American Journal of Medical Genetics Part A. 143A(8). 830–838. 47 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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