Cynthia C. Morton

32.7k citations

281 papers · 18.9k indexed · 3 hit papers · h-index 73

Molecular Biology top 0.5%
Sensory Systems top 0.05%
Genetics top 0.5%
Immunology top 1%
Oncology top 1%

Co-authors: Walter E. Nance Stanislawa Weremowicz Philip Leder Ilan R. Kirsch Bradley J. Quade Rebecca Taub Nahid G. Robertson Daniel Swan
Topics: Hearing, Cochlea, Tinnitus, Genetics (47 papers)Uterine Myomas and Treatments (46 papers)Genomic variations and chromosomal abnormalities (43 papers)
Cited by: Sensory Systems Obstetrics and Gynecology Otorhinolaryngology
Journals: Nature Science New England Journal of Medicine
Partner nations: United States United Kingdom China

In The Last Decade

Cynthia C. Morton

272 papers receiving 18.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Newborn Hearing Screening — A Silent Revolution

2006 1.2k citations Cynthia C. Morton et al. New England Journal of Medicine profile →
Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells.

1982 1.1k citations Cynthia C. Morton, Philip Leder et al. profile →
Derivation of Embryonic Stem-Cell Lines from Human Blastocysts

2004 733 citations Chad A. Cowan, Irina Klimanskaya et al. New England Journal of Medicine profile →

Peers

Countries citing papers authored by Cynthia C. Morton

Since Specialization

Citations

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

Fields of papers citing papers by Cynthia C. Morton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cynthia C. Morton. 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 Cynthia C. Morton. The network helps show where Cynthia C. Morton may publish in the future.

Co-authorship network of co-authors of Cynthia C. Morton

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genetic contribution of reproductive traits to risk of uterine leiomyomata: a large-scale, genome-wide, cross-trait analysis 2024 ·American Journal of Obstetrics and Gynecology ·(unknown),Xueyao Wu,C. Scott Gallagher,Danielle Rasooly,Xia Jiang,Cynthia C. Morton	3
2	Chromosomal structural rearrangements implicate long non-coding RNAs in rare germline disorders 2024 ·Human Genetics ·Rebecca Andersen,(unknown),(unknown),T. Sakamoto,Elijah L. Mena,Sami S. Amr,(unknown),Margaret A. Kenna,Caroline D. Robson,Ellen Wilch,(unknown),Raúl E. Piña-Aguilar,Christopher A. Walsh,Cynthia C. Morton	4
3	Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage 2023 ·Gene ·D. David,(unknown),Renata Maria Souza Oliveira,Sofia Dória,Cynthia C. Morton	0
4	Mate-pair genome sequencing reveals structural variants for idiopathic male infertility 2022 ·Human Genetics ·Zirui Dong,(unknown),(unknown),Matthew Hoi Kin Chau,Ye Cao,(unknown),Steven Y. C. Tong,(unknown),Yvonne K. Kwok,(unknown),David Yiu Leung Chan,(unknown),Chi‐Fai Ng,(unknown),Jennifer Sze Man Mak,Tak Yeung Leung,Jacqueline Pui Wah Chung,Cynthia C. Morton,Kwong Wai Choy	3
5	Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape 2020 ·Human Genetics ·D. David,(unknown),(unknown),(unknown),(unknown),(unknown),Raúl E. Piña-Aguilar,Cynthia C. Morton	10
6	First Report of Bilateral External Auditory Canal Cochlin Aggregates (“Cochlinomas”) with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss and a Novel Genetic Variant in COCH Encoding Cochlin 2019 ·Head and Neck Pathology ·(unknown),Nicole J. Boczek,Nahid G. Robertson,Samih H. Nasr,Daniel Jethanamest,Ellen D. McPhail,Paul J. Kurtin,Surendra Dasari,Malinda L. Butz,Cynthia C. Morton,W. Edward Highsmith,Fang Zhou	2
7	Target-enriched massively parallel sequencing for genetic diagnosis of hereditary hearing loss in patients with normal array CGH result. 2018 ·PubMed ·Kwong Wai Choy,Ye Cao,(unknown),Ivan F. M. Lo,Cynthia C. Morton,Tak Yeung Leung	3
8	Identification and function of long non-coding RNA 2013 ·Frontiers in Cellular Neuroscience ·Carl Ernst,Cynthia C. Morton	149
9	Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profiling of the t(12;14) and evidence in support of predisposing genetic heterogeneity 2012 ·Human Molecular Genetics ·Jennelle C. Hodge,Tae‐Min Kim,Jonathan M. Dreyfuss,(unknown),(unknown),(unknown),Bradley J. Quade,Peter J. Park,Elizabeth A. Stewart,Cynthia C. Morton	36
10	Cochlin in the eye: Functional implications 2007 ·Progress in Retinal and Eye Research ·(unknown),Kavita Desai,Jasenka Guduric‐Fuchs,Tiziana Cogliati,Cynthia C. Morton,Sanjoy K. Bhattacharya	27
11	SUMO1 Haploinsufficiency Leads to Cleft Lip and Palate 2006 ·Science ·Fowzan S. Alkuraya,Irfan Saadi,(unknown),Annick Turbé-Doan,Cynthia C. Morton,Richard L. Maas	146
12	Increased Frequencies of Cochlin-Specific T Cells in Patients with Autoimmune Sensorineural Hearing Loss 2006 ·The Journal of Immunology ·(unknown),Hyun-Min Park,Justin M. Johnson,Cengiz Z. Altuntas,Dan Jane‐wit,Ritika Jaini,C. Arturo Solares,Dawn Thomas,Edward J. Ball,Nahid G. Robertson,Cynthia C. Morton,Gordon B. Hughes,Vincent K. Tuohy	80
13	Coffee, Cirrhosis, and Transaminase Enzymes 2006 ·Archives of Internal Medicine ·Arthur L. Klatsky,Cynthia C. Morton,Natalia Udaltsova,Gary Friedman	143
14	Tumor-Associated Endothelial Cells with Cytogenetic Abnormalities 2004 ·Cancer Research ·Kyoko Hida,Yasuhiro Hida,Dhara N. Amin,Alan F. Flint,Dipak Panigrahy,Cynthia C. Morton,Michael Klagsbrun	366
15	Derivation of Embryonic Stem-Cell Lines from Human Blastocystsbreakdown → 2004 ·New England Journal of Medicine ·Chad A. Cowan,Irina Klimanskaya,Jill A. McMahon,(unknown),J. Witmyer,Jacob Zucker,Shunping Wang,Cynthia C. Morton,Andrew P. McMahon,Doug Powers,Douglas A. Melton	733
16	A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis 2000 ·Genes Chromosomes and Cancer ·Carl J. Vaughan,Stanislawa Weremowicz,Marsha M. Goldstein,Mairead Casey,Matthew J. Hart,Rebecca T. Hahn,Richard B. Devereux,Leonard N. Girardi,Frederick J. Schoen,Jonathan A. Fletcher,Cynthia C. Morton,Craig T. Basson	18
17	Disruption of the architectural factor HMGI-C: DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains 1995 ·Cell ·(unknown),Marlena S. Fejzo,(unknown),Xianjin Zhou,Jonathan A. Fletcher,Stanislawa Weremowicz,Cynthia C. Morton,Kiran Chada	363
18	RSK3 Encodes a Novel pp90 ^rsk Isoform with a Unique N-Terminal Sequence: Growth Factor-Stimulated Kinase Function and Nuclear Translocation 1995 ·Molecular and Cellular Biology ·Yi Zhao,Christian Bjørbæk,Stanislawa Weremowicz,Cynthia C. Morton,David E. Moller	120
19	Purification of the Human NF-E2 Complex: cDNA Cloning of the Hematopoietic Cell-Specific Subunit and Evidence for an Associated Partner 1993 ·Molecular and Cellular Biology ·Paul A. Ney,Nancy C. Andrews,Stephen M. Jane,Brian Safer,Mary Purucker,Stanislawa Weremowicz,Cynthia C. Morton,Sabra C. Goff,Stuart H. Orkin,Arthur W. Nienhuis	42
20	Perinatal lethality (ple): A mutation caused by integration of a transgene into distal mouse chromosome 15 1989 ·Genomics ·David R. Beier,Cynthia C. Morton,Aya Leder,(unknown),Philip Leder	18

About Cynthia C. Morton

Cynthia C. Morton is a scholar working on Sensory Systems, Obstetrics and Gynecology and Reproductive Medicine, having authored 281 papers that have together received 18.9k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (47 papers), Uterine Myomas and Treatments (46 papers) and Genomic variations and chromosomal abnormalities (43 papers). The work is most often cited by research in Sensory Systems (3.1k citations), Obstetrics and Gynecology (1.7k citations) and Otorhinolaryngology (767 citations). Cynthia C. Morton has collaborated with scholars based in United States, United Kingdom and China. Frequent co-authors include Walter E. Nance, Stanislawa Weremowicz, Philip Leder, Ilan R. Kirsch, Bradley J. Quade, Rebecca Taub, Nahid G. Robertson, Daniel Swan, Stuart A. Aaronson and Steven R. Tronick. Their work appears in journals such as Nature, Science and New England Journal of Medicine.

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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