Keri Ramsey

1.4k citations

14 papers · 255 indexed · h-index 10

Co-authors: David W. Craig Vinodh Narayanan Gregory G. Heuer Kevin A. Strauss Isabelle Schrauwen Dietrich Stephan Peter B. Crino David A. Ramsay
Topics: Genetics and Neurodevelopmental Disorders (4 papers)Genomics and Rare Diseases (3 papers)RNA Research and Splicing (3 papers)
Cited by: Genetics Cell Biology Molecular Biology
Journals: Nature CommunicationsSHILAP Revista de lepidopterologíaPLoS ONE
Partner nations: United States Canada Belgium

In The Last Decade

Keri Ramsey

14 papers receiving 253 citations

Peers

Countries citing papers authored by Keri Ramsey

Since Specialization

Citations

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

Fields of papers citing papers by Keri Ramsey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Keri Ramsey. 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 Keri Ramsey. The network helps show where Keri Ramsey may publish in the future.

Co-authorship network of co-authors of Keri Ramsey

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Family and caregiver perspectives on gene therapy for Rett syndrome 2024 ·SHILAP Revista de lepidopterología ·Keri Ramsey,(unknown),(unknown),Mark Borgstrom,(unknown),Vinodh Narayanan,(unknown)	2
2	Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: A novel SMS gene variant 2023 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),Newell Belnap,Marcus Naymik,(unknown),Jennifer L. Sloan,(unknown),(unknown),(unknown),Tracy Murray Stewart,Jackson R. Foley,Sampathkumar Rangasamy,Matthew J. Huentelman,Vinodh Narayanan,Keri Ramsey	2
3	Expanding allelic and phenotypic spectrum of ZC4H2‐related disorder: A novel hypomorphic variant and high prevalence of tethered cord 2022 ·Clinical Genetics ·Parith Wongkittichote,Tae‐Ik Choi,(unknown),(unknown),Dwight D. Koeberl,Vinodh Narayanan,Keri Ramsey,Chris Balak,Charles E. Schwartz,Anna M. Cueto‐González,Francina Munell,Cheol‐Hee Kim,Marwan Shinawi	5
4	Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex 2020 ·Nature Communications ·Jinhong Wie,(unknown),(unknown),Vinodh Narayanan,Keri Ramsey,Newell Belnap,Ana M. Claasen,Amanda Courtright,Matt De Both,Matthew J. Huentelman,Sampathkumar Rangasamy,Ryan Richholt,Isabelle Schrauwen,Ashley L. Siniard,(unknown),Kimberly Aranda,Qi Zhang,Yandong Zhou,Dejian Ren	19
5	Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD) 2019 ·Human Genetics ·Lorida Llaci,Keri Ramsey,Newell Belnap,Ana M. Claasen,Chris Balak,Szabolcs Szelinger,(unknown),Ashley L. Siniard,Ryan Richholt,(unknown),Marcus Naymik,Matt De Both,Ignazio S. Piras,David W. Craig,Matthew J. Huentelman,Vinodh Narayanan,Isabelle Schrauwen,Sampathkumar Rangasamy	12
6	Utilizing RNA and outlier analysis to identify an intronic splice‐altering variant inAP4S1in a sibling pair with progressive spastic paraplegia 2019 ·Human Mutation ·(unknown),Szabolcs Szelinger,Newell Belnap,Keri Ramsey,Isabelle Schrauwen,Ana M. Claasen,Leah W. Burke,Ashley L. Siniard,Matthew J. Huentelman,Vinodh Narayanan,David W. Craig	5
7	A novel variant in TAF1 affects gene expression and is associated with X-linked TAF1 intellectual disability syndrome 2018 ·PubMed ·(unknown),Erika Liktor‐Busa,Aubin Moutal,Sara S. Parker,Sydney Rice,Szabolcs Szelinger,(unknown),Michael F. Hammer,Laurel Johnstone,Keri Ramsey,Vinodh Narayanan,Samantha Perez‐Miller,May Khanna,(unknown),Karen A. Lewis,David W. Craig,Edith H. Wang,Rajesh Khanna,Mark A. Nelson	14
8	De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy 2018 ·American Journal of Medical Genetics Part A ·Monica H. Wojcik,Kyoko Okada,Sanjay P. Prabhu,Dan W. Nowakowski,Keri Ramsey,Chris Balak,Sampathkumar Rangasamy,Catherine A. Brownstein,Klaus Schmitz‐Abe,Julie S. Cohen,Ali Fatemi,Jiahai Shi,P. Ellen Grant,Vinodh Narayanan,Hsin‐Yi Henry Ho,Pankaj B. Agrawal	19
9	Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results 2017 ·Seminars in Pediatric Neurology ·(unknown),Keri Ramsey,Newell Belnap,Szabolcs Szelinger,Ashley L. Siniard,Chris Balak,Megan Russell,Ryan Richholt,Matt De Both,Ana M. Claasen,Isabelle Schrauwen,Matthew J. Huentelman,David W. Craig,Sampathkumar Rangasamy,Vinodh Narayanan	9
10	An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach 2016 ·Molecular Genetics and Metabolism Reports ·(unknown),Vinodh Narayanan,Newell Belnap,Keri Ramsey,Theresa A. Grebe	11
11	A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia 2016 ·Molecular Case Studies ·(unknown),Newell Belnap,Ashley L. Siniard,Szabolcs Szelinger,Ana M. Claasen,Ryan Richholt,Matt De Both,Jason J. Corneveaux,Chris Balak,Ignazio S. Piras,Megan Russell,(unknown),Sampathkumar Rangasamy,Keri Ramsey,David W. Craig,Vinodh Narayanan,Matt Huentelman,Isabelle Schrauwen	15
12	A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome 2015 ·PLoS ONE ·Isabelle Schrauwen,Szabolcs Szelinger,Ashley L. Siniard,Ahmet Kurdoglu,Jason J. Corneveaux,Ivana Malenica,Ryan Richholt,Guy Van Camp,Matt De Both,Shanker Swaminathan,(unknown),Keri Ramsey,David W. Craig,Vinodh Narayanan,Matthew J. Huentelman	35
13	A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome 2015 ·Investigative Ophthalmology & Visual Science ·Isabelle Schrauwen,Szabolcs Szelinger,Ashley L. Siniard,Jason J. Corneveaux,Ahmet Kurdoglu,Ryan Richholt,Matt De Both,Ivana Malenica,Shanker Swaminathan,Sampathkumar Rangasamy,Neil Kulkarni,Saunder Bernes,Jeffrey Buchhalter,Keri Ramsey,David W. Craig,Vinodh Narayanan,Matthew J. Huentelman	14
14	Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5 2007 ·Brain ·Erik G. Puffenberger,Kevin A. Strauss,Keri Ramsey,David W. Craig,Dietrich Stephan,(unknown),(unknown),Scott Gottlieb,David A. Ramsay,Victoria Mok Siu,Gregory G. Heuer,Peter B. Crino,D. Holmes Morton	93

About Keri Ramsey

Keri Ramsey is a scholar working on Genetics, Clinical Biochemistry and Molecular Biology, having authored 14 papers that have together received 255 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Genetics (97 citations), Cell Biology (54 citations) and Molecular Biology (163 citations). Keri Ramsey has collaborated with scholars based in United States, Canada and Belgium. Frequent co-authors include David W. Craig, Vinodh Narayanan, Gregory G. Heuer, Kevin A. Strauss, Isabelle Schrauwen, Dietrich Stephan, Peter B. Crino, David A. Ramsay, Scott Gottlieb and Victoria Mok Siu. Their work appears in journals such as Nature Communications, SHILAP Revista de lepidopterología 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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