Lawrence T. Reiter

4.3k citations

71 papers · 2.9k indexed · 1 hit paper · h-index 29

Aging top 2%
Genetics top 1%
- Genetics and Neurodevelopmental Disorders 30
- Genomic variations and chromosomal abnormalities 16
- Genetic Syndromes and Imprinting 15
Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders 9
- Genetic Neurodegenerative Diseases 6
Molecular Biology top 5%
- Congenital heart defects research 10
- Epigenetics and DNA Methylation 10
Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research 12

Co-authors: Michael Gribskov Lorraine Potocki Ethan Bier James R. Lupski T. Murakami Janine M. LaSalle Stormy J. Chamberlain Mark S. LeDoux
Cited by: Aging Genetics Cellular and Molecular Neuroscience
Journals: Nature Communications (1 paper)Nature Genetics (1 paper)Environmental Science & Technology (1 paper)
Partner nations: United States Canada Switzerland

In The Last Decade

Lawrence T. Reiter

70 papers receiving 2.9k citations

Hit Papers

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Peers

Countries citing papers authored by Lawrence T. Reiter

Since Specialization

Citations

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

Fields of papers citing papers by Lawrence T. Reiter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Phase I randomized, observer-blinded, placebo-controlled study of a SARS-CoV-2 mRNA vaccine PTX-COVID19-B Scientific Reports ·Natalia Martín‐Orozco,Noah Vale,Alan Mihic,Talya Amor,Lawrence T. Reiter,Yuko Arita,Reuben Samson,Queenie Hu,Anne‐Claude Gingras,B. Sorenson,Eric G. Marcusson,Piyush M. Patel	2023	5
2	Linoleic acid improves PIEZO2 dysfunction in a mouse model of Angelman Syndrome Nature Communications ·Luis O. Romero,Rebeca Caires,A. Kaitlyn Victor,Juanma Ramírez,Francisco J. Sierra-Valdez,Patrick Walsh,Vincent Truong,Jungsoo Lee,Ugo Mayor,Lawrence T. Reiter,Valeria Vásquez,Julio F. Cordero-Morales	2023	28
3	Properties of beta oscillations in Dup15q syndrome Journal of Neurodevelopmental Disorders ·Vidya Saravanapandian,Joel Frohlich,Joerg F. Hipp,Carly Hyde,(unknown),Peyman Golshani,Edwin H. Cook,Lawrence T. Reiter,Damla Şentürk,Shafali Jeste	2020	16
4	An Unbiased Drug Screen for Seizure Suppressors in Duplication 15q Syndrome Reveals 5-HT1A and Dopamine Pathway Activation as Potential Therapies Biological Psychiatry ·Bidisha Roy,Jungsoo Han,Kevin A. Hope,Tracy L. Peters,Glen E. Palmer,Lawrence T. Reiter	2020	9
5	The Drosophila Gene Sulfateless Modulates Autism-Like Behaviors Frontiers in Genetics ·Kevin A. Hope,Daniel Flatten,Peter Cavitch,Ben May,James S. Sutcliffe,Janis M. O’Donnell,Lawrence T. Reiter	2019	14
6	Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses JMIR Research Protocols ·Oluwaseun Ajayi,Ebony Smith,Teeradache Viangteeravat,Eunice Y. Huang,Naga Satya V Rao Nagisetty,Nora Urraca,Laina Lusk,Brenda Finucane,Dimitrios Arkilo,Jennifer Young,Shafali Jeste,Ronald L. Thibert,Lawrence T. Reiter,(unknown)	2017	5
7	Glial overexpression of Dube3a causes seizures and synaptic impairments in Drosophila concomitant with down regulation of the Na+/K+ pump ATPα Neurobiology of Disease ·Kevin A. Hope,Mark S. LeDoux,Lawrence T. Reiter	2017	23
8	A recurrent de novo missense mutation in UBTF causes developmental neuroregression Human Molecular Genetics ·Camilo Toro,Roderick Hori,May Christine V. Malicdan,Cynthia J. Tifft,Amy Goldstein,William A. Gahl,David R. Adams,Harper B Fauni,Lynne A. Wolfe,Jianfeng Xiao,Mohammad Moshahid Khan,Jun Tian,Kevin A. Hope,Lawrence T. Reiter,Michel G. Tremblay,Tom Moss,Alexis L. Franks,Chris Balak,Mark S. LeDoux	2017	29
9	Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome Journal of Neurodevelopmental Disorders ·Charlotte DiStefano,Amanda C. Gulsrud,Scott Huberty,Connie Kasari,Edwin H. Cook,Lawrence T. Reiter,Ronald L. Thibert,Shafali Jeste	2016	48
10	Effects of hTERT immortalization on osteogenic and adipogenic differentiation of dental pulp stem cells Data in Brief ·Ikbale El-Ayachi,Sarita Goorha,Lawrence T. Reiter,Gustavo A. Miranda‐Carboni	2016	16
11	Characterization of neurons from immortalized dental pulp stem cells for the study of neurogenetic disorders Stem Cell Research ·Nora Urraca,Rawaha Memon,Ikbale El-Iyachi,Sarita Goorha,Colleen Valdez,Quynh T. Tran,Reese S. Scroggs,Gustavo A. Miranda‐Carboni,Martin Donaldson,Dave Bridges,Lawrence T. Reiter	2015	30
12	The Interstitial Duplication 15q11.2‐q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature Autism Research ·Nora Urraca,Julie Cleary,Victoria E. Brewer,Enikö K. Pivnick,Kathryn McVicar,Ronald L. Thibert,N. Carolyn Schanen,Carmen Esmer,Dustin Lamport,Lawrence T. Reiter	2013	116
13	Altered Serotonin, Dopamine and Norepinepherine Levels in 15q Duplication and Angelman Syndrome Mouse Models PLoS ONE ·M. Febin Farook,Michael DeCuypere,Keith Hyland,Toru Takumi,Mark S. LeDoux,Lawrence T. Reiter	2012	35
14	A Single-Tube Quantitative High-Resolution Melting Curve Method for Parent-of-Origin Determination of 15q Duplications Genetic Testing and Molecular Biomarkers ·Nora Urraca,Lea K. Davis,Edwin H. Cook,N. Carolyn Schanen,Lawrence T. Reiter	2010	8
15	Drosophila Ube3a regulates monoamine synthesis by increasing GTP cyclohydrolase I activity via a non-ubiquitin ligase mechanism Neurobiology of Disease ·Faiza Ferdousy,William J. Bodeen,Kyle C. Summers,Olugbenga M. Doherty,Oneil A. Wright,Nahed Elsisi,George M. Hilliard,Janis M. O’Donnell,Lawrence T. Reiter	2010	32
16	Drosophila Orthologues to Human Disease Genes: An Update on Progress Progress in nucleic acid research and molecular biology ·Sergey Doronkin,Lawrence T. Reiter	2008	13
17	Recent efforts to model human diseases in vivo in Drosophila Fly ·Cathie M. Pfleger,Lawrence T. Reiter	2008	4
18	The 1.4-Mb CMT1A Duplication/HNPP Deletion Genomic Region Reveals Unique Genome Architectural Features and Provides Insights into the Recent Evolution of New Genes Genome Research ·Ken Inoue,Ken Dewar,Nicholas Katsanis,Lawrence T. Reiter,Eric S. Lander,Keri Devon,Dudley Wyman,James R. Lupski,Bruce W. Birren	2001	111
19	Localization of mariner DNA Transposons in the Human Genome by PRINS Genome Research ·Lawrence T. Reiter,Thomas Liehr,Bernd Rautenstrauß,Hugh M. Robertson,James R. Lupski	1999	18
20	The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs Human Molecular Genetics ·Lawrence T. Reiter	1997	69

About Lawrence T. Reiter

Lawrence T. Reiter is a scholar working on Genetics, Aging and Genetics, having authored 71 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (30 papers), Genomic variations and chromosomal abnormalities (16 papers), Genetic Syndromes and Imprinting (15 papers), Autism Spectrum Disorder Research (12 papers), Congenital heart defects research (10 papers), Epigenetics and DNA Methylation (10 papers), Hereditary Neurological Disorders (9 papers) and Genetic Neurodegenerative Diseases (6 papers). The work is most often cited by research in Aging (149 citations), Genetics (1.4k citations) and Cellular and Molecular Neuroscience (622 citations). Lawrence T. Reiter has collaborated with scholars based in United States, Canada and Switzerland. Frequent co-authors include Michael Gribskov, Lorraine Potocki, Ethan Bier, James R. Lupski, T. Murakami, Janine M. LaSalle, Stormy J. Chamberlain, Ethan Bier, Mark S. LeDoux and Thearith Koeuth. Their work appears in journals such as Nature Communications, Nature Genetics and Environmental Science & Technology.

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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