Lawrence T. Reiter

4.3k citations

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

Molecular Biology top 5%
Genetics top 1%
Cellular and Molecular Neuroscience top 5%
Cognitive Neuroscience top 5%
Plant Science top 10%

Co-authors: Michael Gribskov Lorraine Potocki Ethan Bier James R. Lupski T. Murakami Janine M. LaSalle Stormy J. Chamberlain Mark S. LeDoux
Topics: Genetics and Neurodevelopmental Disorders (30 papers)Genomic variations and chromosomal abnormalities (16 papers)Genetic Syndromes and Imprinting (15 papers)
Cited by: Aging Genetics Cellular and Molecular Neuroscience
Journals: Nature Communications Nature Genetics Environmental Science & Technology
Partner nations: United States Canada Switzerland

In The Last Decade

Lawrence T. Reiter

70 papers receiving 2.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A Systematic Analysis of Human Disease-Associated Gene Sequences In Drosophila melanogaster

2001 679 citations Lawrence T. Reiter et al. Genome Research profile →

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 of co-authors of Lawrence T. Reiter

This figure shows the co-authorship network connecting the top 25 collaborators of Lawrence T. Reiter. A scholar is included among the top collaborators of Lawrence T. Reiter 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 Lawrence T. Reiter. Lawrence T. Reiter 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	Phase I randomized, observer-blinded, placebo-controlled study of a SARS-CoV-2 mRNA vaccine PTX-COVID19-B 2023 ·Scientific Reports ·Natalia Martín‐Orozco,Noah Vale,(unknown),(unknown),Lawrence T. Reiter,Yuko Arita,Reuben Samson,Queenie Hu,Anne‐Claude Gingras,(unknown),Eric G. Marcusson,Piyush M. Patel	5
2	Linoleic acid improves PIEZO2 dysfunction in a mouse model of Angelman Syndrome 2023 ·Nature Communications ·Luis O. Romero,Rebeca Caires,(unknown),Juanma Ramírez,Francisco J. Sierra-Valdez,Patrick Walsh,Vincent Truong,(unknown),Ugo Mayor,Lawrence T. Reiter,Valeria Vásquez,Julio F. Cordero-Morales	28
3	Properties of beta oscillations in Dup15q syndrome 2020 ·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	16
4	An Unbiased Drug Screen for Seizure Suppressors in Duplication 15q Syndrome Reveals 5-HT1A and Dopamine Pathway Activation as Potential Therapies 2020 ·Biological Psychiatry ·Bidisha Roy,Jungsoo Han,Kevin A. Hope,Tracy L. Peters,Glen E. Palmer,Lawrence T. Reiter	9
5	The Drosophila Gene Sulfateless Modulates Autism-Like Behaviors 2019 ·Frontiers in Genetics ·Kevin A. Hope,(unknown),(unknown),(unknown),James S. Sutcliffe,Janis M. O’Donnell,Lawrence T. Reiter	14
6	Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses 2017 ·JMIR Research Protocols ·(unknown),(unknown),(unknown),Eunice Y. Huang,(unknown),Nora Urraca,(unknown),Brenda Finucane,Dimitrios Arkilo,(unknown),Shafali Jeste,Ronald L. Thibert,Lawrence T. Reiter,(unknown)	5
7	Glial overexpression of Dube3a causes seizures and synaptic impairments in Drosophila concomitant with down regulation of the Na+/K+ pump ATPα 2017 ·Neurobiology of Disease ·Kevin A. Hope,Mark S. LeDoux,Lawrence T. Reiter	23
8	A recurrent de novo missense mutation in UBTF causes developmental neuroregression 2017 ·Human Molecular Genetics ·Camilo Toro,Roderick Hori,May Christine V. Malicdan,Cynthia J. Tifft,Amy Goldstein,William A. Gahl,David R. Adams,(unknown),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	29
9	Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome 2016 ·Journal of Neurodevelopmental Disorders ·Charlotte DiStefano,Amanda C. Gulsrud,Scott Huberty,Connie Kasari,Edwin H. Cook,Lawrence T. Reiter,Ronald L. Thibert,Shafali Jeste	48
10	Effects of hTERT immortalization on osteogenic and adipogenic differentiation of dental pulp stem cells 2016 ·Data in Brief ·(unknown),Sarita Goorha,Lawrence T. Reiter,Gustavo A. Miranda‐Carboni	16
11	Characterization of neurons from immortalized dental pulp stem cells for the study of neurogenetic disorders 2015 ·Stem Cell Research ·Nora Urraca,(unknown),(unknown),Sarita Goorha,(unknown),Quynh T. Tran,Reese S. Scroggs,Gustavo A. Miranda‐Carboni,Martin Donaldson,Dave Bridges,Lawrence T. Reiter	30
12	The Interstitial Duplication 15q11.2‐q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature 2013 ·Autism Research ·Nora Urraca,(unknown),Victoria E. Brewer,Enikö K. Pivnick,Kathryn McVicar,Ronald L. Thibert,N. Carolyn Schanen,Carmen Esmer,(unknown),Lawrence T. Reiter	116
13	Altered Serotonin, Dopamine and Norepinepherine Levels in 15q Duplication and Angelman Syndrome Mouse Models 2012 ·PLoS ONE ·(unknown),Michael DeCuypere,Keith Hyland,Toru Takumi,Mark S. LeDoux,Lawrence T. Reiter	35
14	A Single-Tube Quantitative High-Resolution Melting Curve Method for Parent-of-Origin Determination of 15q Duplications 2010 ·Genetic Testing and Molecular Biomarkers ·Nora Urraca,Lea K. Davis,Edwin H. Cook,N. Carolyn Schanen,Lawrence T. Reiter	8
15	Drosophila Ube3a regulates monoamine synthesis by increasing GTP cyclohydrolase I activity via a non-ubiquitin ligase mechanism 2010 ·Neurobiology of Disease ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),George M. Hilliard,Janis M. O’Donnell,Lawrence T. Reiter	32
16	Drosophila Orthologues to Human Disease Genes: An Update on Progress 2008 ·Progress in nucleic acid research and molecular biology ·(unknown),Lawrence T. Reiter	13
17	Recent efforts to model human diseases in vivo in Drosophila 2008 ·Fly ·Cathie M. Pfleger,Lawrence T. Reiter	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 2001 ·Genome Research ·Ken Inoue,Ken Dewar,Nicholas Katsanis,Lawrence T. Reiter,Eric S. Lander,(unknown),(unknown),James R. Lupski,Bruce W. Birren	111
19	Localization of mariner DNA Transposons in the Human Genome by PRINS 1999 ·Genome Research ·Lawrence T. Reiter,Thomas Liehr,Bernd Rautenstrauß,Hugh M. Robertson,James R. Lupski	18
20	The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs 1997 ·Human Molecular Genetics ·Lawrence T. Reiter	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) and Genetic Syndromes and Imprinting (15 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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