Cynthia C. Morton

Also affiliated with Brigham and Women's Hospital, Harvard University

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 3%percentile

1.5Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Maternal and Newborn Hospital Outcomes of Perinatal SARS-CoV-2 Infection: A National Registry

PEDIATRICS(2023)10.1542/peds.2022-059595

Top 13%

1.5DataRank

Top 13%43 citations

Dustin D. Flannery, Kimberly Barnette, Trace Getzlaff, Shiva Gautam, Miren B. Dhudasia +88 more

Papers

Driven by 23 papers — median percentile 87. Top paper: “Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss”.

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.010

N/A

1.6DataRank · unranked

76 citations

Maxim B. Freidin, Linda Broer, Berthe C. Oosterloo, Shuyang Yao, Yitian Zhou +65 more

Maternal and Newborn Hospital Outcomes of Perinatal SARS-CoV-2 Infection: A National Registry

PEDIATRICS(2023)10.1542/peds.2022-059595

Top 13%

1.5DataRank

Top 13%43 citations

Dustin D. Flannery, Kimberly Barnette, Trace Getzlaff, Shiva Gautam, Miren B. Dhudasia +88 more

Loss of LDAH associated with prostate cancer and hearing loss

Human Molecular Genetics(2018)10.1093/hmg/ddy310

N/A

1.0DataRank · unranked

19 citations

Ming Chen, Richard C Sallari, Maura Cotter, Kristen E. Wong, Nahid G. Robertson +32 more

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

Human Reproduction(2023)10.1093/humrep/dead247

N/A

0.505DataRank · unranked

28 citations

Scott D. Gordon, David L Duffy, Nikki Hubers, Sally Mortlock, Jeffrey J. Beck +52 more

Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development

Journal of Clinical Investigation(2020)10.1172/jci136951

N/A

0.442DataRank · unranked

18 citations

Clemer Abad, Filiz Başak Cengiz, Serhat Seyhan, Armağan İncesulu, Shengru Guo +14 more

A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Scientific Reports(2023)10.1038/s41598-023-40037-4

N/A

0.269DataRank · unranked

5 citations

Shotaro Kishikawa, Vijay Gupta, Natalia T. Leach, Yiping Shen, Oana Moldovan +14 more

Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics

Genetics in Medicine(2017)10.1038/gim.2016.171

N/A

0.208DataRank · unranked

3 citations

Athena M. Cherry, Beverly S. Emanuel, Uta Francke, H. Eugene Hoyme, Laird G. Jackson +9 more

Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

Nature Communications(2022)10.1038/s41467-022-33222-y

N/A

0.170DataRank · unranked

2 citations

Netta Mäkinen, Holly R. Harris, Nilüfer Rahmioğlu, Outi Uimari, James P. Cook +54 more

AnFiSA: An open-source computational platform for the analysis of sequencing data for rare genetic disease

Journal of Biomedical Informatics(2022)10.1016/j.jbi.2022.104174

N/A

0.165DataRank · unranked

2 citations

D. Etin, S I Trifonov, Viktoria Evdokimova, V. Ulitin, Jun Shen +15 more

Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals

Diagnostics(2022)10.3390/diagnostics12051098

N/A

0DataRank · unranked

10 citations

Baosheng Zhu, Jichun Tan, Yichun Guan, Cynthia C. Morton, Guangxiu Lu +1 more

Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases

Frontiers in Genetics(2022)10.3389/fgene.2022.1022918

N/A

0DataRank · unranked

0 citations

D. David, Claudia Gonzaga‐Jauregui, Cynthia C. Morton, Cinthya Zepeda‐Mendoza, Zirui Dong

Cochlin Deficiency Protects Against Noise-Induced Hearing Loss

Frontiers in Molecular Neuroscience(2021)10.3389/fnmol.2021.670013

N/A

0DataRank · unranked

15 citations

Lukas D. Landegger, Nahid G. Robertson, Saša Vasilijić, Cynthia C. Morton, Konstantina M. Stanković +1 more

Genetics of Childhood Hearing Loss

Otolaryngologic Clinics of North America(2021)10.1016/j.otc.2021.08.008

N/A

0DataRank · unranked

19 citations

Cynthia C. Morton, Calli O. Mitchell

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

UNC Libraries(2020)10.17615/tdb3-bx52

N/A

0DataRank · unranked

0 citations

Hemant Bengani, Joseph A. Marsh, Angela M. Kaindl, Koh-ichiro Yoshiura, Katharina Steindl +73 more

A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Research Square(2023)10.21203/rs.3.rs-2572736/v1

N/A

0DataRank · unranked

1 citations

Shotaro Kishikawa, Vijay Gupta, Natalia T. Leach, Yiping Shen, Oana Moldovan +14 more

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.07.555775

N/A

0DataRank · unranked

0 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +13 more

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.006

N/A

0DataRank · unranked

23 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +17 more

Genetic contribution of reproductive traits to risk of uterine leiomyomata: a large-scale, genome-wide, cross-trait analysis

American Journal of Obstetrics and Gynecology(2024)10.1016/j.ajog.2023.12.040

N/A

0DataRank · unranked

3 citations

Xueyao Wu, C. Scott Gallagher, Danielle Rasooly, Xia Jiang, Cynthia C. Morton +1 more

A comprehensive genome-wide cross-trait analysis of sexual factors and uterine leiomyoma

PLoS Genetics(2024)10.1371/journal.pgen.1011268

N/A

0DataRank · unranked

1 citations

Changfeng Xiao, Danielle Rasooly, Xunying Zhao, Cynthia C. Morton, Xia Jiang +2 more

Genetic counselors’ perspectives and experiences with workplace genetic testing: Results of a national survey

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103483

N/A

0DataRank · unranked

0 citations

Elizabeth Charnysh, Subhamoy Pal, Jonathan M. Reader, Katherine Hendy, W. Gregory Feero +32 more

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w

N/A

0DataRank · unranked

17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more

Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape

Human Genetics(2020)10.1007/s00439-020-02121-x

N/A

0DataRank · unranked

11 citations

João Parente Freixo, Joana Fino, Inês Carvalho, Mariana Marques, Manuela Pinto Cardoso +3 more

Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.05.015

N/A

0DataRank · unranked

20 citations

Chenghan Xiao, Zhitong Han, Li Zhang, Xunying Zhao, Yu Hao +7 more

Cynthia C. Morton

Indexed papers

Top data-sharing exemplar

Papers