Works by Conrad, Donald F.
Results: 35
The Sertoli cell expressed gene secernin‐1 (Scrn1) is dispensable for male fertility in the mouse.
- Published in:
- Developmental Dynamics, 2021, v. 250, n. 7, p. 922, doi. 10.1002/dvdy.299
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- Article
Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 217, doi. 10.1007/s00439-020-02236-1
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- Article
A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse.
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- Human Genetics, 2021, v. 140, n. 1, p. 155, doi. 10.1007/s00439-020-02159-x
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- Publication type:
- Article
DeNovoGear: de novo indel and point mutation discovery and phasing.
- Published in:
- Nature Methods, 2013, v. 10, n. 10, p. 985, doi. 10.1038/nmeth.2611
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- Article
Mapping copy number variation by population-scale genome sequencing.
- Published in:
- Nature, 2011, v. 470, n. 7332, p. 59, doi. 10.1038/nature09708
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- Article
Origins and functional impact of copy number variation in the human genome.
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- Nature, 2010, v. 464, n. 7289, p. 704, doi. 10.1038/nature08516
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- Article
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
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- Nature, 2010, v. 464, n. 7289, p. 713, doi. 10.1038/nature08979
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- Article
Multiplex shRNA Screening of Germ Cell Development by in Vivo Transfection of Mouse Testis.
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- G3: Genes | Genomes | Genetics, 2017, v. 7, n. 1, p. 247, doi. 10.1534/g3.116.036087
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- Article
Reduced burden of very large and rare CNVs in bipolar affective disorder.
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- Bipolar Disorders, 2013, v. 15, n. 8, p. 893, doi. 10.1111/bdi.12125
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- Article
Consensus label propagation with graph convolutional networks for single-cell RNA sequencing cell type annotation.
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- Bioinformatics, 2023, v. 39, n. 6, p. 1, doi. 10.1093/bioinformatics/btad360
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- Publication type:
- Article
SATINN: an automated neural network-based classification of testicular sections allows for high-throughput histopathology of mouse mutants.
- Published in:
- Bioinformatics, 2022, v. 38, n. 23, p. 5288, doi. 10.1093/bioinformatics/btac673
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- Article
Estimating error models for whole genome sequencing using mixtures of Dirichlet-multinomial distributions.
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- Bioinformatics, 2017, v. 33, n. 15, p. 2322, doi. 10.1093/bioinformatics/btx133
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- Publication type:
- Article
DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-04714-4
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- Article
Inverted duplications on acentric markers: mechanism of formation.
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- Human Molecular Genetics, 2009, v. 18, n. 12, p. 2241, doi. 10.1093/hmg/ddp160
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- Article
Recurrent 16p11.2 microdeletions in autism.
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- Human Molecular Genetics, 2008, v. 17, n. 4, p. 628
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- Article
Deleterious genetic changes in AGTPBP1 result in teratozoospermia with sperm head and flagella defects.
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- Journal of Cellular & Molecular Medicine, 2024, v. 28, n. 2, p. 1, doi. 10.1111/jcmm.18031
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- Article
Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1592-3
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- Article
Genetic mutation of Cep76 results in male infertility due to abnormal sperm tail composition.
- Published in:
- Life Science Alliance, 2024, v. 7, n. 6, p. 1, doi. 10.26508/lsa.202302452
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- Article
Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1134849
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- Article
Clonal Architecture of Secondary Acute Myeloid Leukemia Defined by Single-Cell Sequencing.
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- PLoS Genetics, 2014, v. 10, n. 7, p. 1, doi. 10.1371/journal.pgen.1004462
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- Article
Cis and Trans Effects of Human Genomic Variants on Gene Expression.
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- PLoS Genetics, 2014, v. 10, n. 7, p. 1, doi. 10.1371/journal.pgen.1004461
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- Article
Rhesus macaque fetal and placental growth demographics: A resource for laboratory animal researchers.
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- American Journal of Primatology, 2023, v. 85, n. 8, p. 1, doi. 10.1002/ajp.23526
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- Article
Population Differentiation as an Indicator of Recent Positive Selection in Humans: An Empirical Evaluation.
- Published in:
- Genetics, 2009, v. 183, n. 3, p. 1065, doi. 10.1534/genetics.109.107722
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- Publication type:
- Article
Validating single-cell genomics for the study of renal development.
- Published in:
- Kidney International, 2014, v. 86, n. 5, p. 1049, doi. 10.1038/ki.2014.104
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- Article
Variation in genome-wide mutation rates within and between human families.
- Published in:
- Nature Genetics, 2011, v. 43, n. 7, p. 712, doi. 10.1038/ng.862
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- Article
Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.
- Published in:
- Nature Genetics, 2010, v. 42, n. 5, p. 385, doi. 10.1038/ng.564
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- Article
The population genetics of structural variation.
- Published in:
- Nature Genetics, 2007, v. 39, p. S30, doi. 10.1038/ng2042
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- Article
A worldwide survey of haplotype variation and linkage disequilibrium in the human genome.
- Published in:
- Nature Genetics, 2006, v. 38, n. 11, p. 1251, doi. 10.1038/ng1911
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- Article
A high-resolution survey of deletion polymorphism in the human genome.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 75, doi. 10.1038/ng1697
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- Article
Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia.
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- PLoS Genetics, 2020, v. 16, n. 8, p. 1, doi. 10.1371/journal.pgen.1008691
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- Article
Haplotypic Background of a Private Allele at High Frequency in the Americas.
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- Molecular Biology & Evolution, 2009, v. 26, n. 5, p. 995, doi. 10.1093/molbev/msp024
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- Article
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12522-w
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- Article
Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management.
- Published in:
- 2022
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- Publication type:
- journal article
A Protein Allergen Microarray Detects Specific IgE to Pollen Surface, Cytoplasmic, and Commercial Allergen Extracts.
- Published in:
- PLoS ONE, 2010, v. 5, n. 4, p. 1, doi. 10.1371/journal.pone.0010174
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- Publication type:
- Article