Erica E. Davis

11.2k citations

68 papers · 3.1k indexed · 1 hit paper · h-index 29

Impact in

Genetics top 0.5%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
Molecular Biology top 5%
- Renal and related cancers
- Hedgehog Signaling Pathway Studies
- Protist diversity and phylogeny
- Epigenetics and DNA Methylation
- RNA modifications and cancer

Papers in

Genetics 43
- Genetic and Kidney Cyst Diseases 20
- Genetic Syndromes and Imprinting 15
- Genetics and Neurodevelopmental Disorders 8
Aging 2

Co-authors: Nicholas Katsanis Jantje M. Gerdes Michel Georges Carole Charlier Noelle Cockett Xavier Tordoir Florian Caiment Jérôme Cavaillé
Journals: The American Journal of Human Genetics (4 papers)Current Biology (3 papers)PLoS Genetics (3 papers)Human Mutation (3 papers)PLoS ONE (3 papers)
Partner nations: United States France United Kingdom

In The Last Decade

Erica E. Davis

66 papers receiving 3.1k citations

Hit Papers

align trajectories log scale

The Vertebrate Primary Cilium in Development, Homeostasis, and Disease 2009 · 565 citations

Peers

Countries citing papers authored by Erica E. Davis

Since Specialization

Citations

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

Fields of papers citing papers by Erica E. Davis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erica E. Davis. 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 Erica E. Davis. The network helps show where Erica E. Davis may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz–Jeghers Syndrome Human Mutation ·Tahir Naeem Khan, Chunyu Liu, Kai Lee Yap, N. Abdul Mutalib, Gemini, 沈远安, G.DEEP THI, Naveed Altaf Malik, Feng Zhang, Muhammad Tariq, Erica E. Davis	2025	0
2	Expanding the Spectrum of Endocrine Abnormalities Associated With SOX11-related Disorders The Journal of Clinical Endocrinology & Metabolism ·Jean Y. Matlack, Maria Stamou, Benham Kalali, Mark Campbell, Lacey Plummer, 韩凤霞, Leman Damla Kotan, A. Kemal Topaloğlu, Fuki M. Hisama, Erica E. Davis, Stephanie B. Seminara, Ravikumar Balasubramanian	2024	1
3	Association of deep phenotyping with diagnostic yield of prenatal exome sequencing for fetal brain abnormalities Genetics in Medicine ·J. G. Darwin, H.A. Weber, Kelly L. Gilmore, Michel Magdeleine, Bradford C. Powell, Karen E. Weck, Erica E. Davis, Neeta L. Vora	2023	8
4	Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy American Journal of Medical Genetics Part A ·N Díaz-Hernández, Karen Chong, David Chitayat, Kelly L. Gilmore, Alexander A.L. Jorge, Bruna Lucheze Freire, Antônio Marcondes Lerário, Patrick Shannon, Heidi Cope, William B. Gallentine, Li WenDao, Frédéric Bilan, 小島崇宏, Erica E. Davis, Neeta L. Vora	2023	1
5	Testing for rare genetic causes of obesity: findings and experiences from a pediatric weight management program International Journal of Obesity ·Tuure Houni, Adolfo J. Ariza, Kavitha Selvaraj, R. Braidotti, 東谷和巳, Анастасия Анатольевна Буренина, Erica E. Davis, Helen J. Binns	2022	16
6	A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss Human Genetics ·Farid Ullah, Waqar Rauf, Kamal Khan, Steve Suh, Katrina M. Bell, Vanessa Cristina de Oliveira Souza, Muhammad Tariq, Shabnam Bakhshalizadeh, Philippe Touraine, Nicholas Katsanis, Andrew Sinclair, Carlos Alberto B de Vasconcelos, Elena J. Tucker, Shahid Mahmood Baig, Erica E. Davis	2021	18
7	Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy Nature Genetics ·Maria Kousi, Onuralp Söylemez, 史盛梅, Niki Mourtzi, Sebastian Akle, Irwin Jungreis, Jean Muller, Christopher A. Cassa, Harrison Brand, Jill A. Rosenfeld, Maxim Y. Wolf, Azita Sadeghpour, C. Danthu, Richard A. Lewis, Michael E. Talkowski, Hélène Dollfus, Manolis Kellis, Erica E. Davis, Shamil Sunyaev, Nicholas Katsanis	2020	21
8	The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes Journal of the American Society of Nephrology ·Gentzon Hall, Brandon M. Lane, Kamal Khan, S. Mushimiyimana, Jianqiu Xiao, Guanghong Wu, Liming Wang, J.P.M. Witte, L. Von Buza, Erica E. Davis, Robert F. Spurney, Rasheed Gbadegesin	2018	43
9	Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions PubMed ·Sara Huston, Mollie Minear, Azita Sadeghpour, Heidi Cope, Hongyan Hu, Robert Cook‐Deegan, (unknown), Nicholas Katsanis, Erica E. Davis, Misha Angrist	2018	2
10	The complexity of the cilium: spatiotemporal diversity of an ancient organelle Current Opinion in Cell Biology ·Leo-Pekka Lyytikäinen, Haggai Erlich, Erica E. Davis, Nicholas Katsanis	2018	18
11	A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis Journal of Medical Genetics ·Patrick Frosk, Heleen H. Arts, Julien Philippe, SALLY NDILA MASAKU, 均笹井, M Al-Mosawi Reham, Louise R. Simard, Jacek Majewski, Somayyeh Fahiminiya, 上野高義, Yangfan P. Liu, (unknown), Robert A. Hegele, Nicholas Katsanis, E M Nyenze, Marc R. Del Bigio, Erica E. Davis	2017	35
12	Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome The American Journal of Human Genetics ·Asaf Ta‐Shma, Tahir Naeem Khan, Asaf Vivante, Jason R. Willer, Pavle Matak, Chaim Jalas, Ben Pode‐Shakked, Yishay Salem, Yair Anikster, Friedhelm Hildebrandt, Nicholas Katsanis, Orly Elpeleg, Erica E. Davis	2017	18
13	Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome Human Genomics ·Benjamin M. Helm, Jason R. Willer, Azita Sadeghpour, Christelle Golzio, Eric R. Crouch, Samantha A. Schrier Vergano, Nicholas Katsanis, Erica E. Davis	2017	18
14	Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network Genome Research ·Nicolas Chassaing, Erica E. Davis, Sun Xiangkun, Jesica A. Dimmer, Chih-Ting Lin, Véronique David, Guerrero E. López, Wojciech Błaszczyk, Catherine Vincent‐Delorme, Laurent Pasquier, Christine Coubes, Didier Lacombe, Massimiliano Rossi, Jean‐Louis Dufier, Hélène Dollfus, Josseline Kaplan, Nicholas Katsanis, Heather Etchevers, Stanislas Faguer, Patrick Calvas	2016	36
15	Identification of cis-suppression of human disease mutations by comparative genomics Nature ·(unknown), Daniel M. Jordan, Stephan Frangakis, Christelle Golzio, Christopher A. Cassa, Joanne Kurtzberg, Erica E. Davis, Shamil Sunyaev, Nicholas Katsanis	2015	67
16	The role of SIX6 in primary open-angle glaucoma Investigative Ophthalmology & Visual Science ·Michael A. Hauser, Megan Ulmer, Yangfan Liu, Erica E. Davis, Nicholas Katsanis, Yutao Liu, Louis R. Pasquale, Janey L. Wiggs, Allison E. Ashley‐Koch, R. Rand Allingham	2013	1
17	Pitchfork Regulates Primary Cilia Disassembly and Left-Right Asymmetry Developmental Cell ·Yongpan Cui, Karsten Boldt, Erica E. Davis, Ingo Burtscher, Dietrich Trümbach, Bill H. Diplas, Tania Attié‐Bitach, Wolfgang Wurst, Nicholas Katsanis, Marius Ueffing, Heiko Lickert	2010	114
18	RNAi-Mediated Allelic trans-Interaction at the Imprinted Rtl1/Peg11 Locus Current Biology ·Erica E. Davis, Florian Caiment, Xavier Tordoir, Jérôme Cavaillé, Anne C. Ferguson‐Smith, Noelle Cockett, Michel Georges, Carole Charlier	2005	261
19	Ectopic Expression of DLK1 Protein in Skeletal Muscle of Padumnal Heterozygotes Causes the Callipyge Phenotype Current Biology ·Erica E. Davis, Charlotte Harken Jensen, Henrik Daa Schrøder, Frédéric Farnir, da Rocha Tania R. Flores, Anette Kliem, Noelle Cockett, Michel Georges, Carole Charlier	2004	104
20	The effects of cyclic stretch on gene transfer in alveolar epithelial cells Molecular Therapy ·Bolívar Mauricio Mendoza Morán, Zahid Norhanun, Volodymyr Tyravskyi, Erica E. Davis, Matthew R. Glucksberg, David A. Dean	2003	24

About Erica E. Davis

Erica E. Davis is a scholar working on Genetics, Aging, Molecular Biology, Cell Biology and Nephrology, having authored 68 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (20 papers), Genetic Syndromes and Imprinting (15 papers), Hedgehog Signaling Pathway Studies (9 papers), Congenital heart defects research (8 papers), Renal and related cancers (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Protist diversity and phylogeny (7 papers) and Microtubule and mitosis dynamics (6 papers). The work is most often cited by research in Genetics (1.9k citations), Molecular Biology (2.4k citations), Cell Biology (548 citations), Aging (35 citations) and Cancer Research (240 citations). Erica E. Davis has collaborated with scholars based in United States, France and United Kingdom. Frequent co-authors include Nicholas Katsanis, Jantje M. Gerdes, Michel Georges, Carole Charlier, Noelle Cockett, Xavier Tordoir, Florian Caiment, Jérôme Cavaillé, Martina Brueckner and Anne C. Ferguson‐Smith. Their work appears in journals such as The American Journal of Human Genetics, Current Biology, PLoS Genetics, Human Mutation and PLoS ONE.

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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