Adele Schneider

3.5k citations

67 papers · 2.2k indexed · h-index 23

Genetics top 2%
- Ocular Disorders and Treatments 36
- Congenital Ear and Nasal Anomalies 24
- Genomic variations and chromosomal abnormalities 6
- Craniofacial Disorders and Treatments 5
Genetics top 1%
- Ocular Disorders and Treatments 36
- Congenital Ear and Nasal Anomalies 24
- Genomic variations and chromosomal abnormalities 6
- Craniofacial Disorders and Treatments 5
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 6
Ophthalmology top 5%
Molecular Biology top 10%
- Retinal Development and Disorders 8
- Hedgehog Signaling Pathway Studies 5
Surgery
- Reconstructive Facial Surgery Techniques 14

Co-authors: Tanya Bardakjian Anthony R. Gregg Linda M. Reis Elena V. Semina Rebecca C. Tyler David Fitzpatrick Veronica van Heyningen Kathleen A. Williamson
Cited by: Genetics Pediatrics, Perinatology and Child Health
Journals: Human Molecular Genetics (4 papers)Clinical Genetics (4 papers)European Journal of Human Genetics (2 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Adele Schneider

63 papers receiving 2.1k citations

Peers

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

The 25 scholars most cited alongside Adele 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 Schneider Line = papers co-authored together Adele Schneider links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Dominant variants in PRR12 result in unilateral or bilateral complex microphthalmia Clinical Genetics ·Linda M. Reis,Deborah M. Costakos,Patricia G. Wheeler,Tanya Bardakjian,Adele Schneider,S. Fung,Elena V. Semina	2020	9
2	Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis Journal of Human Genetics ·K. V. Mardia,Julie Plaisancié,Pierre Bitoun,Marta Cortón,Ana Arteche‐López,Carmen Ayuso,Adele Schneider,Crystal Champion,Christian Gilissen,Olivier Roche,Maurice Linnane,Patrick Calvas,Anne Slavotinek,Nicola Ragge,Nicolas Chassaing	2020	5
3	Ocular manifestations of PACS1 mutation Journal of American Association for Pediatric Ophthalmology and Strabismus ·Maria Pefkianaki,Adele Schneider,Jenina Capasso,Barry N. Wasserman,Tanya Bardakjian,Alex V. Levin	2018	10
4	Expanded Carrier Screening in Reproductive Medicine—Points to Consider Obstetrics and Gynecology ·Janice G. Edwards,Gerald L. Feldman,Judith D. Goldberg,Anthony R. Gregg,Mary E. Norton,Nancy C. Rose,Adele Schneider,Katie Stoll,Ronald J. Wapner,Michael S. Watson	2015	247
5	Knowledge, attitudes, and barriers to carrier screening for the Ashkenazi Jewish panel: a Florida experience Journal of Community Genetics ·S. MacLaren,G W Ettle,Elizabeth Herman,Yoon-Joong Park,Adele Schneider,Jodi D. Hoffman,So-yeon Lee,Deborah Barbouth	2014	8
6	ACMG Position Statement on Prenatal/Preconception Expanded Carrier Screening Obstetrical & Gynecological Survey ·Wayne W. Grody,Barry H. Thompson,Anthony R. Gregg,Lora Bean,Kristin G. Monaghan,Adele Schneider,Roger V. Lebo	2013	5
7	ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm Human Molecular Genetics ·Mani Yavi,Hana Abouzeid,Ghada Gawdat,Andi Muh Israq Burhanuddin,Tong Xiao,Tanya Bardakjian,Adele Schneider,Alex Choi,Eric Jorgenson,Herwig Baier,Olivier Collinet,Daniel F. Schorderet,Anne Slavotinek	2013	57
8	A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family Clinical Genetics ·Wy Ching Ng,Francesca Pasutto,Georgina Timson,Meiyun Chen,Geoffrey Watson,Adele Schneider,Ganna TVERDOVA,John Grigg,Martin Zenker,Robyn V. Jamieson	2012	13
9	The genetics of anophthalmia and microphthalmia Current Opinion in Ophthalmology ·Tanya Bardakjian,Adele Schneider	2011	59
10	VAX1mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of aVAX1phenotype in humans Human Mutation ·Anne Slavotinek,Ryan Chao,Tomáš Vacı́k,Mani Yavi,Hana Abouzeid,Tanya Bardakjian,Adele Schneider,Gary M. Shaw,Elliott H. Sherr,Greg Lemke,Iza Veliscek,Daniel F. Schorderet	2011	56
11	Clinical report of microphthalmia and optic nerve coloboma associated with a de novo microdeletion of chromosome 16p11.2 American Journal of Medical Genetics Part A ·Tanya Bardakjian,Simon C.M. Kwok,Anne Slavotinek,Adele Schneider	2010	19
12	FOXE3 plays a significant role in autosomal recessive microphthalmia American Journal of Medical Genetics Part A ·Linda M. Reis,Rebecca C. Tyler,Adele Schneider,Tanya Bardakjian,Joan M. Stoler,Serge B. Melançon,Elena V. Semina	2010	44
13	Association of a de novo16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes BMC Medical Genetics ·Tanya Bardakjian,Adele Schneider,David Ng,Jennifer J. Johnston,Leslie G. Biesecker	2009	18
14	Population‐based Tay‐Sachs screening among Ashkenazi Jewish young adults in the 21st century: Hexosaminidase a enzyme assay is essential for accurate testing American Journal of Medical Genetics Part A ·Adele Schneider,Sachiko Nakagawa,RH Vanderlinde,Aerlangga Aerlangga,Joel Charrow,Kirk Aleck,Jodi D. Hoffman,Megan Altman,David N. Finegold,Wei Sun,Andrew Spencer,Gebiana Hgairtety,Seong-Soo,Stephen Apfelroth,Nicole Schreiber‐Agus,Susan J. Gross	2009	18
15	Role ofSOX2Mutations in Human Hippocampal Malformations and Epilepsy Epilepsia ·Sanjay M. Sisodiya,Nicola Ragge,Gianpiero L. Cavalleri,Ann Hever,Birgit Lorenz,Adele Schneider,Kathleen A. Williamson,John Stevens,S. L. Free,Pamela J. Thompson,Veronica van Heyningen,David Fitzpatrick	2006	70
16	SOX2 anophthalmia syndrome American Journal of Medical Genetics Part A ·Nicola Ragge,Birgit Lorenz,Adele Schneider,Kate Bushby,Luisa De Sanctis,Ugo de Sanctis,Alison Salt,J. R. O. Collin,Anthony J. Vivian,S. L. Free,Pamela J. Thompson,Kathleen A. Williamson,Sanjay M. Sisodiya,Veronica van Heyningen,David Fitzpatrick	2005	160
17	Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR Nature Genetics ·David Ng,Nalin Thakker,Connie M. Corcoran,Dian Donnai,Rahat Perveen,Adele Schneider,Donald W. Hadley,Cynthia J. Tifft,Liqun Zhang,Andrew O.M. Wilkie,Jasper J. van der Smagt,Robert J. Gorlin,Shawn M. Burgess,Vivian J. Bardwell,Graeme C. Black,Leslie G. Biesecker	2004	237
18	Absent thoracolumbar spine: prenatal sonography of a new lethal skeletal anomaly. Journal of Ultrasound in Medicine ·Mindy M. Horrow,John S. Schroeder,Adele Schneider,Nayere Zaeri	1995	2
19	Duplication 9q34→qter identified by chromosome painting American Journal of Medical Genetics ·Nancy B. Spinner,J. N. Lucas,M. Poggensee,A. MacEwen Peach,Adele Schneider	1993	24
20	A Program for Improving the Psychosocial Outcome of Infants with Bronchopulmonary Dysplasia (BPD) Frank S. Pidcock,池田大輔,Yin Ruoji,Elias Jabbour,Steven Bachrach,Adele Schneider,Masakatsu Kurogi	1988	2

About Adele Schneider

Adele Schneider is a scholar working on Genetics, Genetics and Immunology and Allergy, having authored 67 papers that have together received 2.2k indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (36 papers), Congenital Ear and Nasal Anomalies (24 papers), Reconstructive Facial Surgery Techniques (14 papers), Retinal Development and Disorders (8 papers), Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Hedgehog Signaling Pathway Studies (5 papers) and Craniofacial Disorders and Treatments (5 papers). The work is most often cited by research in Genetics (502 citations), Genetics (1.2k citations) and Pediatrics, Perinatology and Child Health (366 citations). Adele Schneider has collaborated with scholars based in United States, United Kingdom and Canada. Frequent 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, Roger V. Lebo and Mary E. Norton. Their work appears in journals such as Human Molecular Genetics, Clinical Genetics, European Journal of Human Genetics, Genetics in Medicine 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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