Megan T. Cho

7.5k citations

27 papers · 838 indexed · h-index 20

Genetics top 5%
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 12
- Genomic variations and chromosomal abnormalities 7
- BRCA gene mutations in cancer 5
Molecular Biology
- RNA modifications and cancer 3
- RNA regulation and disease 2
- Epigenetics and DNA Methylation 2
Cognitive Neuroscience
Clinical Biochemistry
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 3

Co-authors: Kyle Retterer Wendy K. Chung Berivan Baskin Marwan Shinawi Ganka Douglas Jane Juusola Kristin G. Monaghan Daniel J. Parente
Cited by: Genetics Molecular Biology Cognitive Neuroscience
Journals: The American Journal of Human Genetics (2 papers)Journal of Medical Genetics (4 papers)Cold Spring Harbor Perspectives in Medicine (1 paper)
Partner nations: United States Canada Netherlands

In The Last Decade

Megan T. Cho

27 papers receiving 805 citations

Peers

Countries citing papers authored by Megan T. Cho

Since Specialization

Citations

This map shows the geographic impact of Megan T. Cho'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 Megan T. Cho with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Megan T. Cho more than expected).

Fields of papers citing papers by Megan T. Cho

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Megan T. Cho. 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 Megan T. Cho. The network helps show where Megan T. Cho may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Evolving Roles of Genetic Counselors in the Clinical Laboratory Cold Spring Harbor Perspectives in Medicine ·Megan T. Cho,Carrie Guy	2019	6
2	De novo pathogenic variants in neuronal differentiation factor 2 (NEUROD2) cause a form of early infantile epileptic encephalopathy Journal of Medical Genetics ·Annalisa G. Sega,Emily K. Mis,Kristin Lindstrom,Saadet Mercimek‐Andrews,Weizhen Ji,Megan T. Cho,Jane Juusola,Monica Konstantino,Lauren Jeffries,Mustafa K. Khokha,Saquib A. Lakhani	2018	25
3	Congenital methemoglobinemia type II in a 5‐year‐old boy Clinical Case Reports ·Elizabeth A. Mannino,Thomas Pluim,Jacob M. Wessler,Megan T. Cho,Jane Juusola,Samantha A. Schrier Vergano	2017	6
4	De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism Molecular Case Studies ·Akemi Tanaka,Megan T. Cho,Rebecca Willaert,Kyle Retterer,Yuri A. Zárate,Katie Bosanko,Vikki Stefans,Kimihiko Oishi,Amy Williamson,Golder N. Wilson,Alice Basinger,Tina Barbaro‐Dieber,Lucia Ortega,Susanna Sorrentino,Melissa K. Gabriel,Ilse J. Anderson,María J. Guillen Sacoto,Rhonda E. Schnur,Wendy K. Chung	2017	23
5	Missense variants in the chromatin remodeler CHD1 are associated with neurodevelopmental disability Journal of Medical Genetics ·Genay Pilarowski,Hilary J. Vernon,Carolyn Applegate,Leandros Boukas,Megan T. Cho,Christina A. Gurnett,Paul J. Benke,Erin Beaver,Jennifer Heeley,Līvija Medne,Ian D. Krantz,Meron Azage,Dmitriy Niyazov,Lindsay B. Henderson,Ingrid M. Wentzensen,Berivan Baskin,María J. Guillen Sacoto,Gregory D. Bowman,Hans T. Björnsson	2017	38
6	A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects Neurogenetics ·David B. Beck,Megan T. Cho,Francisca Millan,Carin Yates,Mark Hannibal,Bridget O’Connor,Marwan Shinawi,Anne M. Connolly,Darrel Waggoner,Sara Halbach,Brad Angle,Victoria R. Sanders,Yufeng Shen,Kyle Retterer,Amber Begtrup,Renkui Bai,Wendy K. Chung	2016	25
7	De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features Human Genetics ·Volkan Okur,Megan T. Cho,Lindsay B. Henderson,Kyle Retterer,Michael Schneider,Shannon G. Sattler,Dmitriy Niyazov,Meron Azage,Sharon E. Smith,Jonathan Picker,Sharyn A. Lincoln,Mark A. Tarnopolsky,Lauren Brady,Hans T. Björnsson,Carolyn Applegate,Amy Dameron,Rebecca Willaert,Berivan Baskin,Jane Juusola,Wendy K. Chung	2016	53
8	Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects The American Journal of Human Genetics ·Lia Boyle,Mirjam M. C. Wamelink,Gajja S. Salomons,Birthe Roos,Ana Pop,Andrew Dauber,Vivian Hwa,Melissa Andrew,Jessica Douglas,Murray Feingold,Nancy Kramer,Sulagna C. Saitta,Kyle Retterer,Megan T. Cho,Amber Begtrup,Kristin G. Monaghan,Julia Wynn,Wendy K. Chung	2016	33
9	Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder American Journal of Medical Genetics Part A ·Francisca Millan,Megan T. Cho,Kyle Retterer,Kristin G. Monaghan,Renkui Bai,Patrik Vitazka,David B. Everman,Brooke Smith,Brad Angle,Victoria H. J. Roberts,LaDonna Immken,Honey Nagakura,Marc DiFazio,Elliott H. Sherr,Eden Haverfield,Bethany Friedman,Aida Telegrafi,Jane Juusola,Wendy K. Chung,Sherri J. Bale	2016	42
10	Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity American Journal of Medical Genetics Part A ·Daniel J. Parente,Caryn Garriga,Berivan Baskin,Ganka Douglas,Megan T. Cho,Gabriel C. Araujo,Marwan Shinawi	2016	79
11	Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females The American Journal of Human Genetics ·Jennifer Bain,Megan T. Cho,Aida Telegrafi,Ashley Wilson,Susan Sklower Brooks,Christina Botti,Gordon C. Gowans,Leigh Anne Autullo,Vidya Krishnamurthy,Marcia Willing,Tomi L. Toler,Bruria Ben-Zev,Orly Elpeleg,Yufeng Shen,Kyle Retterer,Kristin G. Monaghan,Wendy K. Chung	2016	43
12	De novo PHIP-predicted deleterious variants are associated with developmental delay, intellectual disability, obesity, and dysmorphic features Molecular Case Studies ·Emily Webster,Megan T. Cho,Nora Alexander,Sonal Desai,Sakkubai Naidu,Mir Reza Bekheirnia,Andrea M. Lewis,Kyle Retterer,Jane Juusola,Wendy K. Chung	2016	40
13	De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia Journal of Medical Genetics ·Esther R. Berko,Megan T. Cho,Christine M. Eng,Yunru Shao,David A. Sweetser,Jessica L. Waxler,Nathaniel H. Robin,Fallon Brewer,Sandra Donkervoort,Payam Mohassel,Carsten G. Bönnemann,Martin G. Bialer,Christine Moore,Lynne A. Wolfe,Cynthia J. Tifft,Yufeng Shen,Kyle Retterer,Francisca Millan,Wendy K. Chung	2016	44
14	Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features Neurogenetics ·Hallie Steinfeld,Megan T. Cho,Kyle Retterer,Rick Person,G. Bradley Schaefer,Noelle R. Danylchuk,Saleem Malik,Stephanie Burns Wechsler,Patricia G. Wheeler,Koen L.I. van Gassen,Pauline Terhal,Virginie J. M. Verhoeven,Marjon A. van Slegtenhorst,Kristin G. Monaghan,Lindsay B. Henderson,Wendy K. Chung	2016	30
15	FTO variant associated with malformation syndrome American Journal of Medical Genetics Part A ·Luis Rohena,Michelle Lawson,Edwin R. Guzman,Mythily Ganapathi,Megan T. Cho,Eden Haverfield,Kwame Anyane‐Yeboa	2015	14
16	De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial features Molecular Case Studies ·Akemi Tanaka,Megan T. Cho,Kyle Retterer,Julie R. Jones,C. Nowak,Jessica Douglas,Yong‐hui Jiang,Allyn McConkie‐Rosell,G. Bradley Schaefer,Julie Kaylor,Omar Abdul Rahman,Aida Telegrafi,Bethany Friedman,Ganka Douglas,Kristin G. Monaghan,Wendy K. Chung	2015	25
17	De novo mutations in PURA are associated with hypotonia and developmental delay Molecular Case Studies ·Akemi Tanaka,Renkui Bai,Megan T. Cho,Kwame Anyane‐Yeboa,Priyanka Ahimaz,Ashley Wilson,Fran Kendall,Beverly N. Hay,Timothy J. M. Moss,Monica Nardini,Mislen Bauer,Kyle Retterer,Jane Juusola,Wendy K. Chung	2015	49
18	De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism Neurogenetics ·Linshan Shang,Lindsay B. Henderson,Megan T. Cho,Donald Petrey,Chin-To Fong,Katrina Haude,Natasha Shur,Julie Lundberg,Natalie Hauser,Jason Carmichael,Jeffrey W. Innis,Jane L. Schuette,Yvonne W. Wu,Shailesh Asaikar,Margaret A. Pearson,Leandra Folk,Kyle Retterer,Kristin G. Monaghan,Wendy K. Chung	2015	52
19	De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly Molecular Case Studies ·Yizhou Ye,Megan T. Cho,Kyle Retterer,Nora Alexander,Tawfeg Ben‐Omran,Mariam Al‐Mureikhi,Ingrid Cristian,Patricia G. Wheeler,Carrie Crain,Dina J. Zand,Veronique Weinstein,Hilary J. Vernon,Rebecca McClellan,Vidya Krishnamurthy,Patrik Vitazka,Francisca Millan,Wendy K. Chung	2015	39
20	Mutations in ARID2 are associated with intellectual disabilities Neurogenetics ·Linshan Shang,Megan T. Cho,Kyle Retterer,Leandra Folk,Jennifer B. Humberson,Luis Rohena,Alpa Sidhu,Sheila Saliganan,Alejandro Iglesias,Patrik Vitazka,Jane Juusola,Anne O’Donnell‐Luria,Yufeng Shen,Wendy K. Chung	2015	43

About Megan T. Cho

Megan T. Cho is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Virology, having authored 27 papers that have together received 838 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (12 papers), Genomic variations and chromosomal abnormalities (7 papers), BRCA gene mutations in cancer (5 papers), Prenatal Screening and Diagnostics (3 papers), RNA modifications and cancer (3 papers), RNA regulation and disease (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (462 citations), Molecular Biology (508 citations) and Cognitive Neuroscience (79 citations). Megan T. Cho has collaborated with scholars based in United States, Canada and Netherlands. Frequent co-authors include Kyle Retterer, Wendy K. Chung, Berivan Baskin, Marwan Shinawi, Ganka Douglas, Jane Juusola, Jane Juusola, Kristin G. Monaghan, Daniel J. Parente and Gabriel C. Araujo. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Cold Spring Harbor Perspectives in 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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