Co-Authors
This is a "connection" page, showing publications co-authored by MARY DICKINSON and JASON HEANEY.
Connection Strength
1.232
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Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles. BMC Biol. 2018 Jun 21; 16(1):69.
Score: 0.157
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A comprehensive atlas of AAV tropism in the mouse. Mol Ther. 2025 Jan 25.
Score: 0.062
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Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypes. BMC Genomics. 2025 Jan 20; 26(1):48.
Score: 0.062
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Alzheimer's disease risk gene CD2AP is a dose-sensitive determinant of synaptic structure and plasticity. Hum Mol Genet. 2024 10 07; 33(20):1815-1832.
Score: 0.061
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Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines. Sci Rep. 2024 09 30; 14(1):22626.
Score: 0.061
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A Comprehensive Atlas of AAV Tropism in the Mouse. bioRxiv. 2024 Sep 10.
Score: 0.061
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Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity. Commun Biol. 2023 06 10; 6(1):626.
Score: 0.056
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Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice. Mamm Genome. 2023 06; 34(2):180-199.
Score: 0.056
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Genome-wide screening reveals the genetic basis of mammalian embryonic eye development. BMC Biol. 2023 02 03; 21(1):22.
Score: 0.054
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Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes. Sci Rep. 2022 12 01; 12(1):20791.
Score: 0.054
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Mendelian gene identification through mouse embryo viability screening. Genome Med. 2022 10 13; 14(1):119.
Score: 0.053
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AAV5 delivery of CRISPR-Cas9 supports effective genome editing in mouse lung airway. Mol Ther. 2022 Jan 05; 30(1):238-243.
Score: 0.050
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COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
Score: 0.049
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The NIH Somatic Cell Genome Editing program. Nature. 2021 04; 592(7853):195-204.
Score: 0.048
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A resource of targeted mutant mouse lines for 5,061 genes. Nat Genet. 2021 04; 53(4):416-419.
Score: 0.048
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Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density. PLoS Genet. 2020 12; 16(12):e1009190.
Score: 0.047
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A global Slc7a7 knockout mouse model demonstrates characteristic phenotypes of human lysinuric protein intolerance. Hum Mol Genet. 2020 08 03; 29(13):2171-2184.
Score: 0.046
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Soft windowing application to improve analysis of high-throughput phenotyping data. Bioinformatics. 2020 03 01; 36(5):1492-1500.
Score: 0.044
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The Deep Genome Project. Genome Biol. 2020 02 03; 21(1):18.
Score: 0.044
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Human and mouse essentiality screens as a resource for disease gene discovery. Nat Commun. 2020 01 31; 11(1):655.
Score: 0.044
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Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 03 07; 104(3):422-438.
Score: 0.041
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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features. Am J Hum Genet. 2017 Apr 06; 100(4):676-688.
Score: 0.036