Alisha Wilkens

1.3k total citations
20 papers, 438 citations indexed

About

Alisha Wilkens is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Alisha Wilkens has authored 20 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Alisha Wilkens's work include Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (5 papers) and Congenital heart defects research (4 papers). Alisha Wilkens is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (5 papers) and Congenital heart defects research (4 papers). Alisha Wilkens collaborates with scholars based in United States, Japan and Germany. Alisha Wilkens's co-authors include Ian D. Krantz, Kosuke Izumi, Nancy B. Spinner, Laura K. Conlin, Elaine H. Zackai, Matthew A. Deardorff, Lindsey Campbell, Sarah E. Noon, Hongbin Liu and Sulagna C. Saitta and has published in prestigious journals such as PLoS ONE, BMC Bioinformatics and Genetics in Medicine.

In The Last Decade

Alisha Wilkens

18 papers receiving 425 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alisha Wilkens United States	13	255	239	104	67	61	20	438
Dinah Clark United States	15	250 1.0×	495 2.1×	57 0.5×	73 1.1×	97 1.6×	21	711
Barbara Utermann Austria	13	177 0.7×	128 0.5×	100 1.0×	62 0.9×	64 1.0×	18	336
Janice C. Palumbos United States	8	161 0.6×	245 1.0×	56 0.5×	28 0.4×	32 0.5×	13	391
L Korniszewski Poland	12	249 1.0×	274 1.1×	28 0.3×	51 0.8×	85 1.4×	26	498
Jennifer McCallum United States	5	112 0.4×	280 1.2×	23 0.2×	36 0.5×	41 0.7×	5	355
Teresa Palladino Italy	9	141 0.6×	123 0.5×	30 0.3×	25 0.4×	52 0.9×	15	246
Jiale Xiang China	9	88 0.3×	172 0.7×	20 0.2×	82 1.2×	85 1.4×	24	345
Sarah Rickard United Kingdom	5	267 1.0×	291 1.2×	110 1.1×	6 0.1×	68 1.1×	7	385
Ahmet Karagüzel Türkiye	11	95 0.4×	236 1.0×	62 0.6×	14 0.2×	222 3.6×	24	458
Polona Le Quesne Stabej United Kingdom	14	167 0.7×	348 1.5×	25 0.2×	10 0.1×	123 2.0×	18	535

Countries citing papers authored by Alisha Wilkens

Since Specialization

Citations

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

Fields of papers citing papers by Alisha Wilkens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alisha Wilkens

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

All Works

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20 of 20 papers shown

Matalon, Dena R., Elizabeth Bhoj, Dong Li, et al.. (2023). Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome. American Journal of Medical Genetics Part A. 191(4). 977–982.

Izumi, Kosuke, Rebecca Ganetzky, Gerald Wertheim, et al.. (2023). Co-Occurrence of Pallister-Killian Syndrome and Burkitt Lymphoma in a Patient with Near-Normal Neurocognitive Development. Molecular Syndromology. 14(4). 303–309.

Guan, Qiaoning, Jorune Balciuniene, Kajia Cao, et al.. (2018). AUDIOME: a tiered exome sequencing–based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss. Genetics in Medicine. 20(12). 1600–1608. 27 indexed citations

Ahrens‐Nicklas, Rebecca C., George K. E. Umanah, Neal Sondheimer, et al.. (2017). Precision therapy for a new disorder of AMPA receptor recycling due to mutations in ATAD1. Neurology Genetics. 3(1). e130–e130. 30 indexed citations

Noon, Sarah E., E Schwartz, Alisha Wilkens, et al.. (2016). Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic. American Journal of Medical Genetics Part A. 170(10). 2523–2530. 36 indexed citations

Santos, Maria Emília, Alisha Wilkens, Ian D. Krantz, & Yaning Wu. (2016). Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 172(2). 109–116. 6 indexed citations

Izumi, Kosuke, Katsunori Fujiki, Maninder Kaur, et al.. (2015). Elevation of insulin‐like growth factor binding protein‐2 level in Pallister–Killian syndrome: Implications for the postnatal growth retardation phenotype. American Journal of Medical Genetics Part A. 167(6). 1268–1274. 3 indexed citations

Izumi, Kosuke, Sarah E. Noon, Alisha Wilkens, & Ian D. Krantz. (2014). NKX2.5 mutation identification on exome sequencing in a patient with heterotaxy. European Journal of Medical Genetics. 57(10). 558–561. 12 indexed citations

Kaur, Maninder, Kosuke Izumi, Alisha Wilkens, et al.. (2014). Genome-Wide Expression Analysis in Fibroblast Cell Lines from Probands with Pallister Killian Syndrome. PLoS ONE. 9(10). e108853–e108853. 11 indexed citations

10.

Masino, Aaron J., Elizabeth T. DeChene, Matthew C. Dulik, et al.. (2014). Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology. BMC Bioinformatics. 15(1). 248–248. 43 indexed citations

11.

Wilkens, Alisha, et al.. (2014). Cardiac manifestations of Pallister–Killian syndrome. American Journal of Medical Genetics Part A. 164(5). 1130–1135. 15 indexed citations

12.

Francey, Lauren J., Ellen Tsai, Yaru Zhao, et al.. (2013). Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations. American Journal of Medical Genetics Part A. 161(9). 2148–2157. 16 indexed citations

13.

Kalish, Jennifer M., Laura K. Conlin, Sogol Mostoufi‐Moab, et al.. (2013). Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low‐Level Uniparental Disomy. American Journal of Medical Genetics Part A. 161(5). 993–1001. 15 indexed citations

14.

Murray, Brittney, Nuria Amat‐Alarcon, Alisha Wilkens, et al.. (2013). A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio‐oculo‐facial syndrome. American Journal of Medical Genetics Part A. 161(2). 371–376. 6 indexed citations

15.

Kalish, Jennifer M., Laura K. Conlin, Tricia Bhatti, et al.. (2013). Clinical features of three girls with mosaic genome‐wide paternal uniparental isodisomy. American Journal of Medical Genetics Part A. 161(8). 1929–1939. 57 indexed citations

16.

Izumi, Kosuke, Alisha Wilkens, James R. Treat, Howard B. Pride, & Ian D. Krantz. (2013). Novel MBTPS2 Missense Mutation in the N‐Terminus Transmembrane Domain in a Patient with Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome. Pediatric Dermatology. 30(6). e263–4. 5 indexed citations

17.

Izumi, Kosuke, Andrew M. Lippa, Alisha Wilkens, et al.. (2013). Congenital heart defects in oculodentodigital dysplasia: Report of two cases. American Journal of Medical Genetics Part A. 161(12). 3150–3154. 17 indexed citations

18.

Wilkens, Alisha, Hongbin Liu, Kristen Park, et al.. (2012). Novel clinical manifestations in Pallister–Killian syndrome: Comprehensive evaluation of 59 affected individuals and review of previously reported cases. American Journal of Medical Genetics Part A. 158A(12). 3002–3017. 68 indexed citations

19.

Izumi, Kosuke, Laura K. Conlin, Christopher T. Fincher, et al.. (2012). Duplication 12p and Pallister–Killian syndrome: A case report and review of the literature toward defining a Pallister–Killian syndrome minimal critical region. American Journal of Medical Genetics Part A. 158A(12). 3033–3045. 35 indexed citations

20.

Conlin, Laura K., Maninder Kaur, Kosuke Izumi, et al.. (2012). Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister–Killian syndrome. American Journal of Medical Genetics Part A. 158A(12). 3046–3053. 36 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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