Adele Schneider

3.5k total citations
67 papers, 2.2k citations indexed

About

Adele Schneider is a scholar working on Genetics, Genetics and Molecular Biology. According to data from OpenAlex, Adele Schneider has authored 67 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Genetics, 25 papers in Genetics and 20 papers in Molecular Biology. Recurrent topics in Adele Schneider's work include Ocular Disorders and Treatments (36 papers), Congenital Ear and Nasal Anomalies (24 papers) and Reconstructive Facial Surgery Techniques (14 papers). Adele Schneider is often cited by papers focused on Ocular Disorders and Treatments (36 papers), Congenital Ear and Nasal Anomalies (24 papers) and Reconstructive Facial Surgery Techniques (14 papers). Adele Schneider collaborates with scholars based in United States, United Kingdom and Canada. Adele Schneider's co-authors include Tanya Bardakjian, Anthony R. Gregg, Linda M. Reis, Elena V. Semina, Rebecca C. Tyler, David Fitzpatrick, Veronica van Heyningen, Kathleen A. Williamson, Janice G. Edwards and Mary E. Norton and has published in prestigious journals such as Cell, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Adele Schneider

63 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adele Schneider United States 23 1.2k 908 502 383 366 67 2.2k
Sylvie Odent France 36 1.5k 1.2× 2.7k 3.0× 350 0.7× 333 0.9× 562 1.5× 152 3.8k
Maria Hoeltzenbein Germany 23 794 0.6× 899 1.0× 137 0.3× 272 0.7× 237 0.6× 54 2.8k
Ruth Newbury‐Ecob United Kingdom 25 1.3k 1.0× 2.0k 2.2× 222 0.4× 310 0.8× 238 0.7× 64 3.2k
David J. Bunyan United Kingdom 23 979 0.8× 991 1.1× 216 0.4× 208 0.5× 113 0.3× 60 2.0k
Eamonn Sheridan United Kingdom 28 776 0.6× 1.2k 1.3× 170 0.3× 187 0.5× 623 1.7× 74 2.7k
Umadevi Tantravahi United States 29 946 0.8× 1.4k 1.6× 124 0.2× 306 0.8× 416 1.1× 67 2.7k
Shivanand R. Patil United States 24 1.2k 1.0× 1.2k 1.3× 117 0.2× 172 0.4× 418 1.1× 77 2.2k
Eul‐Ju Seo South Korea 24 417 0.3× 796 0.9× 224 0.4× 170 0.4× 156 0.4× 116 1.9k
Nicole Van Regemorter Belgium 24 532 0.4× 1.2k 1.3× 119 0.2× 297 0.8× 380 1.0× 57 2.0k
Rika Kosaki Japan 25 846 0.7× 1.3k 1.4× 204 0.4× 297 0.8× 255 0.7× 113 2.3k

Countries citing papers authored by Adele Schneider

Since Specialization
Citations

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

Fields of papers citing papers by Adele Schneider

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adele Schneider

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

All Works

20 of 20 papers shown
1.
Capasso, Jenina, et al.. (2023). Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis. American Journal of Medical Genetics Part A. 191(4). 1007–1012.
2.
Schneider, Adele, et al.. (2023). P272: Uniparental disomy of chromosome 19 in an individual with oculocutaneous albinism, neurodevelopmental disorder, and failure to thrive. SHILAP Revista de lepidopterología. 1(1). 100300–100300.
3.
Reis, Linda M., et al.. (2022). ARHGAP35 is a novel factor disrupted in human developmental eye phenotypes. European Journal of Human Genetics. 31(3). 363–367. 4 indexed citations
4.
Reis, Linda M., Deborah M. Costakos, Patricia G. Wheeler, et al.. (2020). Dominant variants in PRR12 result in unilateral or bilateral complex microphthalmia. Clinical Genetics. 99(3). 437–442. 9 indexed citations
5.
Plaisancié, Julie, Pierre Bitoun, Marta Cortón, et al.. (2020). Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis. Journal of Human Genetics. 65(5). 487–491. 5 indexed citations
6.
Pefkianaki, Maria, Adele Schneider, Jenina Capasso, et al.. (2018). Ocular manifestations of PACS1 mutation. Journal of American Association for Pediatric Ophthalmology and Strabismus. 22(4). 323–325. 10 indexed citations
7.
Herman, Elizabeth, et al.. (2014). Knowledge, attitudes, and barriers to carrier screening for the Ashkenazi Jewish panel: a Florida experience. Journal of Community Genetics. 5(3). 223–231. 8 indexed citations
8.
Grody, Wayne W., Barry H. Thompson, Anthony R. Gregg, et al.. (2013). ACMG Position Statement on Prenatal/Preconception Expanded Carrier Screening. Obstetrical & Gynecological Survey. 68(12). 785–787. 5 indexed citations
9.
Yavi, Mani, Hana Abouzeid, Ghada Gawdat, et al.. (2013). ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm. Human Molecular Genetics. 22(16). 3250–3258. 57 indexed citations
10.
Bardakjian, Tanya & Adele Schneider. (2011). The genetics of anophthalmia and microphthalmia. Current Opinion in Ophthalmology. 22(5). 309–313. 59 indexed citations
11.
Hollander, Anneke I. den, Tanya Bardakjian, Elias I. Traboulsi, et al.. (2010). Genetic defects of GDF6 in the zebrafish out of sight mutant and in human eye developmental anomalies. BMC Genetics. 11(1). 102–102. 40 indexed citations
12.
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
13.
Bardakjian, Tanya, Adele Schneider, David Ng, Jennifer J. Johnston, & Leslie G. Biesecker. (2009). Association of a de novo16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes. BMC Medical Genetics. 10(1). 137–137. 18 indexed citations
14.
Sisodiya, Sanjay M., Nicola Ragge, Gianpiero L. Cavalleri, et al.. (2006). Role ofSOX2Mutations in Human Hippocampal Malformations and Epilepsy. Epilepsia. 47(3). 534–542. 70 indexed citations
15.
Ragge, Nicola, Birgit Lorenz, Adele Schneider, et al.. (2005). SOX2 anophthalmia syndrome. American Journal of Medical Genetics Part A. 135A(1). 1–7. 160 indexed citations
16.
Horrow, Mindy M., John S. Schroeder, Adele Schneider, & Nayere Zaeri. (1995). Absent thoracolumbar spine: prenatal sonography of a new lethal skeletal anomaly.. Journal of Ultrasound in Medicine. 14(9). 711–713. 2 indexed citations
17.
Spinner, Nancy B., et al.. (1993). Duplication 9q34→qter identified by chromosome painting. American Journal of Medical Genetics. 45(5). 609–613. 24 indexed citations
18.
Schneider, Adele, et al.. (1991). Interstitial deletion of 4(q21q25) in a liveborn male. American Journal of Medical Genetics. 40(1). 77–79. 11 indexed citations
19.
Pidcock, Frank S., et al.. (1988). A Program for Improving the Psychosocial Outcome of Infants with Bronchopulmonary Dysplasia (BPD). 2(4). 251. 2 indexed citations
20.
Yudkoff, Marc, Itzhak Nissim, Adele Schneider, & Stanton Segal. (1981). Cysteamine inhibition of [15N]-glycine turnover in cystinosis and of the glycine cleavage system in vitro. Metabolism. 30(11). 1096–1103. 15 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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