Megan T. Cho

7.5k citations

27 papers · 838 indexed · h-index 20

Co-authors: Kyle Retterer Wendy K. Chung Berivan Baskin Marwan Shinawi Ganka Douglas Jane Juusola Kristin G. Monaghan Daniel J. Parente
Topics: Genetics and Neurodevelopmental Disorders (14 papers)Genomics and Rare Diseases (12 papers)Genomic variations and chromosomal abnormalities (7 papers)
Cited by: Genetics Molecular Biology Cognitive Neuroscience
Journals: The American Journal of Human Genetics Journal of Medical Genetics Cold Spring Harbor Perspectives in Medicine
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 of co-authors of Megan T. Cho

This figure shows the co-authorship network connecting the top 25 collaborators of Megan T. Cho. A scholar is included among the top collaborators of Megan T. Cho 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 Megan T. Cho. Megan T. Cho 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	Evolving Roles of Genetic Counselors in the Clinical Laboratory 2019 ·Cold Spring Harbor Perspectives in Medicine ·Megan T. Cho,(unknown)	6
2	De novo pathogenic variants in neuronal differentiation factor 2 (NEUROD2) cause a form of early infantile epileptic encephalopathy 2018 ·Journal of Medical Genetics ·(unknown),Emily K. Mis,Kristin Lindstrom,Saadet Mercimek‐Andrews,Weizhen Ji,Megan T. Cho,Jane Juusola,Monica Konstantino,(unknown),Mustafa K. Khokha,Saquib A. Lakhani	25
3	Congenital methemoglobinemia type II in a 5‐year‐old boy 2017 ·Clinical Case Reports ·(unknown),(unknown),(unknown),Megan T. Cho,Jane Juusola,Samantha A. Schrier Vergano	6
4	De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism 2017 ·Molecular Case Studies ·Akemi Tanaka,Megan T. Cho,Rebecca Willaert,Kyle Retterer,Yuri A. Zárate,(unknown),(unknown),Kimihiko Oishi,Amy Williamson,Golder N. Wilson,Alice Basinger,(unknown),(unknown),(unknown),(unknown),Ilse J. Anderson,María J. Guillen Sacoto,Rhonda E. Schnur,Wendy K. Chung	23
5	Missense variants in the chromatin remodeler CHD1 are associated with neurodevelopmental disability 2017 ·Journal of Medical Genetics ·Genay Pilarowski,Hilary J. Vernon,Carolyn Applegate,Leandros Boukas,Megan T. Cho,Christina A. Gurnett,Paul J. Benke,(unknown),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	38
6	A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects 2016 ·Neurogenetics ·David B. Beck,Megan T. Cho,Francisca Millan,(unknown),Mark Hannibal,Bridget O’Connor,Marwan Shinawi,Anne M. Connolly,Darrel Waggoner,Sara Halbach,Brad Angle,(unknown),Yufeng Shen,Kyle Retterer,Amber Begtrup,Renkui Bai,Wendy K. Chung	25
7	De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features 2016 ·Human Genetics ·Volkan Okur,Megan T. Cho,Lindsay B. Henderson,Kyle Retterer,Michael Schneider,(unknown),Dmitriy Niyazov,Meron Azage,Sharon E. Smith,Jonathan Picker,Sharyn A. Lincoln,Mark A. Tarnopolsky,Lauren Brady,Hans T. Björnsson,Carolyn Applegate,(unknown),Rebecca Willaert,Berivan Baskin,Jane Juusola,Wendy K. Chung	53
8	Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects 2016 ·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	33
9	Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder 2016 ·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,(unknown),Marc DiFazio,Elliott H. Sherr,Eden Haverfield,Bethany Friedman,Aida Telegrafi,Jane Juusola,Wendy K. Chung,Sherri J. Bale	42
10	Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity 2016 ·American Journal of Medical Genetics Part A ·Daniel J. Parente,(unknown),Berivan Baskin,Ganka Douglas,Megan T. Cho,Gabriel C. Araujo,Marwan Shinawi	79
11	Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females 2016 ·The American Journal of Human Genetics ·Jennifer Bain,Megan T. Cho,Aida Telegrafi,Ashley Wilson,Susan Sklower Brooks,(unknown),Gordon C. Gowans,(unknown),(unknown),Marcia Willing,Tomi L. Toler,(unknown),Orly Elpeleg,Yufeng Shen,Kyle Retterer,Kristin G. Monaghan,Wendy K. Chung	43
12	De novo PHIP-predicted deleterious variants are associated with developmental delay, intellectual disability, obesity, and dysmorphic features 2016 ·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	40
13	De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia 2016 ·Journal of Medical Genetics ·Esther R. Berko,Megan T. Cho,Christine M. Eng,Yunru Shao,David A. Sweetser,Jessica L. Waxler,Nathaniel H. Robin,(unknown),Sandra Donkervoort,Payam Mohassel,Carsten G. Bönnemann,Martin G. Bialer,(unknown),Lynne A. Wolfe,Cynthia J. Tifft,Yufeng Shen,Kyle Retterer,Francisca Millan,Wendy K. Chung	44
14	Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features 2016 ·Neurogenetics ·(unknown),Megan T. Cho,Kyle Retterer,(unknown),G. Bradley Schaefer,(unknown),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	30
15	FTO variant associated with malformation syndrome 2015 ·American Journal of Medical Genetics Part A ·Luis Rohena,(unknown),Edwin R. Guzman,Mythily Ganapathi,Megan T. Cho,Eden Haverfield,Kwame Anyane‐Yeboa	14
16	De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial features 2015 ·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,(unknown),Aida Telegrafi,Bethany Friedman,Ganka Douglas,Kristin G. Monaghan,Wendy K. Chung	25
17	De novo mutations in PURA are associated with hypotonia and developmental delay 2015 ·Molecular Case Studies ·Akemi Tanaka,Renkui Bai,Megan T. Cho,Kwame Anyane‐Yeboa,Priyanka Ahimaz,Ashley Wilson,(unknown),Beverly N. Hay,Timothy J. M. Moss,(unknown),Mislen Bauer,Kyle Retterer,Jane Juusola,Wendy K. Chung	49
18	De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism 2015 ·Neurogenetics ·Linshan Shang,Lindsay B. Henderson,Megan T. Cho,Donald Petrey,Chin-To Fong,Katrina Haude,Natasha Shur,(unknown),Natalie Hauser,Jason Carmichael,Jeffrey W. Innis,Jane L. Schuette,Yvonne W. Wu,(unknown),Margaret A. Pearson,(unknown),Kyle Retterer,Kristin G. Monaghan,Wendy K. Chung	52
19	De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly 2015 ·Molecular Case Studies ·Yizhou Ye,Megan T. Cho,Kyle Retterer,Nora Alexander,Tawfeg Ben‐Omran,Mariam Al‐Mureikhi,Ingrid Cristian,Patricia G. Wheeler,(unknown),Dina J. Zand,(unknown),Hilary J. Vernon,Rebecca McClellan,(unknown),Patrik Vitazka,Francisca Millan,Wendy K. Chung	39
20	Mutations in ARID2 are associated with intellectual disabilities 2015 ·Neurogenetics ·Linshan Shang,Megan T. Cho,Kyle Retterer,(unknown),Jennifer B. Humberson,Luis Rohena,(unknown),(unknown),Alejandro Iglesias,Patrik Vitazka,Jane Juusola,Anne O’Donnell‐Luria,Yufeng Shen,Wendy K. Chung	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) and Genomic variations and chromosomal abnormalities (7 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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