Zöe Powis

3.4k total citations
34 papers, 873 citations indexed

About

Zöe Powis is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Zöe Powis has authored 34 papers receiving a total of 873 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 14 papers in Molecular Biology and 8 papers in Pathology and Forensic Medicine. Recurrent topics in Zöe Powis's work include Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic factors in colorectal cancer (7 papers). Zöe Powis is often cited by papers focused on Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic factors in colorectal cancer (7 papers). Zöe Powis collaborates with scholars based in United States, Philippines and United Kingdom. Zöe Powis's co-authors include Sha Tang, Kelly D. Farwell Hagman, Deepali N. Shinde, Katherine L. Helbig, Cameron Mroske, Shuwei Li, Ingo Helbig, Mari Rossi, Dima El‐Khechen and Mary Helen Black and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the American College of Cardiology and Neurology.

In The Last Decade

Zöe Powis

32 papers receiving 862 citations

Peers

Countries citing papers authored by Zöe Powis

Since Specialization

Citations

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

Fields of papers citing papers by Zöe Powis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zöe Powis

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Expanding the Phenotype of Extremely Early Onset Juvenile Huntington's Disease: A Case Report and Review of Previously Published Cases 2024 ·American Journal of Medical Genetics Part A ·Zöe Powis, (unknown), (unknown), (unknown), Sat Dev Batish	1
2	MAGEL2 ‐related disorders: A study and case series 2019 ·Clinical Genetics ·(unknown), (unknown), (unknown), (unknown), Isabelle Thiffault, Laura Cross, Shivarajan Amudhavalli, (unknown), María Palomares‐Bralo, Sixto García‐Miñáur, Fernando Santos‐Simarro, Zöe Powis, Wendy Alcaraz, Sha Tang, Julie A. Jurgens, Brenda J. Barry, Eleina England, Elizabeth C. Engle, (unknown), Robert Roger Lebel	27
3	Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions 2019 ·Clinical Genetics ·Zöe Powis, Meghan C. Towne, Kelly D. Farwell Hagman, Kirsten Blanco, Erika Palmaer, (unknown), Samin A. Sajan, Kelly Radtke, Timothy Feyma, (unknown), Sha Tang, Christos Sidiropoulos	21
4	When moments matter: Finding answers with rapid exome sequencing 2019 ·Molecular Genetics & Genomic Medicine ·Zöe Powis, Kelly D. Farwell Hagman, Kirsten Blanco, Margaret Au, John M. Graham, Kathryn Singh, Natalie M. Gallant, Linda M. Randolph, Meghan C. Towne, Jesse M. Hunter, Deepali N. Shinde, Erika Palmaer, (unknown), Sha Tang	9
5	Mouse screen reveals multiple new genes underlying mouse and human hearing loss 2019 ·PLoS Biology ·Neil J. Ingham, Selina Pearson, Valerie E. Vancollie, (unknown), Morag A. Lewis, Jing Chen, Annalisa Buniello, (unknown), (unknown), Chi Chung Lam, Felix D. Weiss, Zöe Powis, Pim Suwannarat, Christopher J. Lelliott, Sally J. Dawson, Jacqueline K. White, Karen P. Steel	75
6	Clinical whole‐exome sequencing results impact medical management 2018 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), (unknown), Zöe Powis, Julie S. Cohen, Kelly D. Farwell Hagman	30
7	Clinical germline diagnostic exome sequencing for hereditary cancer: Findings within novel candidate genes are prevalent 2018 ·Cancer Genetics ·Zöe Powis, Carin R. Espenschied, Holly LaDuca, Kelly D. Farwell Hagman, (unknown), Shuwei Li, Hiroto Inaba, Ann M. Mauer, Katherine L. Nathanson, James A. Knost, Elizabeth Chao, Sha Tang	3
8	Exome sequencing in neonates: diagnostic rates, characteristics, and time to diagnosis 2018 ·Genetics in Medicine ·Zöe Powis, Kelly D. Farwell Hagman, Virginia Speare, (unknown), Kirsten Blanco, (unknown), (unknown), David Tilstra, (unknown), Jesse M. Hunter, (unknown), Lina Ghaloul‐Gonzalez, Jerry Vockley, Sha Tang	24
9	Diagnostic exome sequencing identifies GLI 2 haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomalies 2018 ·Clinical Case Reports ·Samin A. Sajan, Zöe Powis, Katherine L. Helbig, (unknown), LaDonna Immken, Sha Tang, Wendy Alcaraz	3
10	Biallelic Mutations in FUT8 Cause a Congenital Disorder of Glycosylation with Defective Fucosylation 2018 ·The American Journal of Human Genetics ·Bobby G. Ng, Gege Xu, (unknown), (unknown), Deepali N. Shinde, Kelly Radtke, Kimiyo Raymond, Carlito B. Lebrilla, Ali Alasmari, Sharon F. Suchy, Zöe Powis, Eissa Faqeih, Susan A. Berry, David F. Kronn, Hudson H. Freeze	53
11	Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders 2017 ·Pediatric Neurology ·Mari Rossi, Dima El‐Khechen, Mary Helen Black, Kelly D. Farwell Hagman, Sha Tang, Zöe Powis	64
12	Clinical diagnostic exome evaluation for an infant with a lethal disorder: genetic diagnosis of TARP syndrome and expansion of the phenotype in a patient with a newly reported RBM10 alteration 2017 ·BMC Medical Genetics ·Zöe Powis, (unknown), Sara Cherny, Igor D. Petrik, Erika Palmaer, Sha Tang, Carolyn Jones	18
13	Identification of a syndrome comprising microcephaly and intellectual disability but not white matter disease associated with a homozygous c.676C>T p.R226W DEAF1 mutation 2016 ·American Journal of Medical Genetics Part A ·(unknown), Zöe Powis, Wendy Alcaraz, Sonal Desai, Kristin Barañano	7
14	Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy 2016 ·Genetics in Medicine ·Katherine L. Helbig, Kelly D. Farwell Hagman, Deepali N. Shinde, Cameron Mroske, Zöe Powis, Shuwei Li, Sha Tang, Ingo Helbig	217
15	Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases 2016 ·Genetics in Medicine ·Kelly D. Farwell Hagman, Deepali N. Shinde, Cameron Mroske, Erica D. Smith, Kelly Radtke, Layla Shahmirzadi, Dima El‐Khechen, Zöe Powis, Elizabeth Chao, Wendy Alcaraz, Katherine L. Helbig, Samin A. Sajan, Mari Rossi, Hsiao‐Mei Lu, Robert Huether, Shuwei Li, Sitao Wu, Mark E. Nuñes, Sha Tang	34
16	Diagnostic Exome Sequencing Is Successful in Providing Diagnoses Among Patients with Intellectual Disability and Developmental Delay: Strong Family History Correlates with an Increased Novel Genetic Etiology Detection Rate (S20.008) 2016 ·Neurology ·(unknown), (unknown), Zöe Powis, (unknown), Sha Tang	0
17	DIAGNOSTIC EXOME SEQUENCING IN PEDIATRIC PATIENTS WITH CONGENITAL HEART DISEASE 2016 ·Journal of the American College of Cardiology ·Zöe Powis, Devon Lamb Thrush, Brigette Tippin Davis, Jill S. Dolinsky	3
18	Diagnostic exome sequencing for patients with a family history of consanguinity: over 38% of positive results are not autosomal recessive pattern 2015 ·Journal of Human Genetics ·Zöe Powis, Kelly D. Farwell, (unknown), Sha Tang	7
19	A Second Family With Dominantly Inherited Isolated Cleft Palate 2010 ·Journal of Craniofacial Surgery ·Zöe Powis, Robert P. Erickson	0
20	Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature 2009 ·Journal of Applied Genetics ·Zöe Powis, Robert P. Erickson	8

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.

Explore authors with similar magnitude of impact