• 2045 Citations
  • 22 h-Index
19942019
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Fingerprint Dive into the research topics where Lawrence T. Reiter is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Drosophila Medicine & Life Sciences
Charcot-Marie-Tooth Disease Medicine & Life Sciences
Angelman Syndrome Medicine & Life Sciences
Genes Medicine & Life Sciences
Autistic Disorder Medicine & Life Sciences
Dental Pulp Medicine & Life Sciences
Drosophila melanogaster Medicine & Life Sciences
Neurons Medicine & Life Sciences

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Research Output 1994 2019

  • 2045 Citations
  • 22 h-Index
  • 47 Article
  • 6 Review article
  • 3 Chapter
  • 2 Comment/debate

A genome-wide enhancer/suppressor screen for Dube3a interacting genes in Drosophila melanogaster

Hope, K. A., McGinn, A. & Reiter, L., Dec 1 2019, In : Scientific Reports. 9, 1, 2382.

Research output: Contribution to journalArticle

Open Access
Drosophila melanogaster
Genome
Genes
Ubiquitin-Protein Ligases
Protein Transport

Mechanisms underlying the EEG biomarker in Dup15q syndrome

Frohlich, J., Reiter, L., Saravanapandian, V., Distefano, C., Huberty, S., Hyde, C., Chamberlain, S., Bearden, C. E., Golshani, P., Irimia, A., Olsen, R. W., Hipp, J. F. & Jeste, S. S., Jul 3 2019, In : Molecular Autism. 10, 1, 29.

Research output: Contribution to journalArticle

Open Access
Electroencephalography
Biomarkers
Phenotype
Midazolam
GABA Modulators

The Drosophila gene sulfateless modulates autism-like behaviors

Hope, K. A., Flatten, D., Cavitch, P., May, B., Sutcliffe, J. S., O'Donnell, J. & Reiter, L. T., Jan 1 2019, In : Frontiers in Genetics. 10, JUN, 574.

Research output: Contribution to journalArticle

Open Access
Autistic Disorder
Drosophila
Genes
Communication
Single Nucleotide Polymorphism
3 Citations (Scopus)

A recurrent de novo missense mutation in UBTF causes developmental neuroregression

C4RCD Research Group, Feb 15 2018, In : Human molecular genetics. 27, 4, p. 691-705 15 p., ddx435.

Research output: Contribution to journalArticle

Missense Mutation
Transcription Factors
DNA-Directed RNA Polymerases
Exome
Dysarthria
2 Citations (Scopus)
Medical Genetics
Missense Mutation
Names
Molecular Biology
corrigendum