Adele S. Schneider

3.5k citations
81 papers · 2.8k · h-index 27

Impact in

  • Genetics top 2%
    • Ocular Disorders and Treatments
    • Congenital Ear and Nasal Anomalies
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Ocular Disorders and Treatments 41
    • Congenital Ear and Nasal Anomalies 22
    • Genomic variations and chromosomal abnormalities 6
    • Craniofacial Disorders and Treatments 5
    • Reconstructive Facial Surgery Techniques 11

Adele S. Schneider

75 papers receiving 2.7k citations

Peers

Adele S. Schneider
Comparison fields: 5 of 107
  • Genetics 1.4k
  • Genetics 484
  • Ophthalmology 169
  • Pediatrics, Perinatology and Child Health 317
  • Molecular Biology 1.0k
Replace David John Bunyan with:
David John Bunyan United Kingdom
Sabine Sigaudy France
Maria Hoeltzenbein Germany
L. Leigh Field Canada
Soo‐Mi Park United Kingdom
Yves Sznajer Belgium
Neeti Ghali United Kingdom
Julie Désir Belgium
Luitgard M. Neumann Germany
Guillermo Antiñolo Spain
Adele S. Schneider relative to David John Bunyan United Kingdom David John Bunyan's profile →
Citations per field
00.5×1.5×2.2×
David John Bunyan · 1×
Citations per year

Countries citing papers authored by Adele S. Schneider

Since Specialization
Citations

This map shows the geographic impact of Adele S. 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 S. 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 S. Schneider more than expected).

Fields of papers citing papers by Adele S. Schneider

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Adele S. Schneider, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Adele S. Schneider Line = papers co-authored together Adele S. Schneider links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 81 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2015286
2 2004268
3 2013198
4 2005193
5 2006185
6 200994
7 201192
8 200678
9 201175
10 201168
11 201365
12 201562
13 201261
14 201460
15 201159
16 200450
17 201049
18 201447
19 201044
20 201343

About Adele S. Schneider

Adele S. Schneider is a scholar working on Genetics, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Ophthalmology, having authored 81 papers that have together received 2.8k indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (41 papers), Congenital Ear and Nasal Anomalies (22 papers), Reconstructive Facial Surgery Techniques (11 papers), Retinal Development and Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers), Hedgehog Signaling Pathway Studies (5 papers) and Craniofacial Disorders and Treatments (5 papers). The work is most often cited by research in Genetics (1.4k citations), Genetics (484 citations), Ophthalmology (169 citations), Pediatrics, Perinatology and Child Health (317 citations) and Molecular Biology (1.0k citations). Adele S. Schneider has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Tanya Bardakjian, Anthony R. Gregg, Linda M. Reis, Elena V. Semina, David R FitzPatrick, Rebecca C. Tyler, Kathleen A. Williamson, Nancy C. Rose, Veronica van Heyningen and Mary E. Norton. Their work appears in journals such as Clinical Genetics, Human Molecular Genetics, European Journal of Human Genetics, The Journal of Pediatrics and American Journal of Obstetrics and Gynecology.

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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