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Maternal Health, Neonatology and Perinatology
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March 16, 2023
Congenital pleuropulmonary blastoma in a newborn with a variant of uncertain significance in DICER1 evaluated by RNA-sequencing
Allison N J Lyle, Timothy J D Ohlsen, Danny E Miller, et al.
G3 (Bethesda, Md.)
|
October 27, 2015
Dynamics of Wolbachia pipientis Gene Expression Across the Drosophila melanogaster Life Cycle
Florence Gutzwiller, Catarina R Carmo, Danny E Miller, et al.
Maternal Health, Neonatology and Perinatology
|
May 25, 2023
Correction to: Congenital pleuropulmonary blastoma in a newborn with a variant of uncertain significance in DICER1 evaluated by RNA-sequencing
Allison N J Lyle, Timothy J D Ohlsen, Danny E Miller, et al.
Nucleic Acids Research
|
July 17, 2025
Splice-modulating antisense oligonucleotides targeting a pathogenic intronic variant in adult polyglucosan body disease correct mis-splicing and restore enzyme activity in patient cells
Ria Thomas, Emily Miyoshi, Hasan O Akman, et al.
Genetics
|
March 6, 2016
Whole-Genome Analysis of Individual Meiotic Events in Drosophila melanogaster Reveals That Noncrossover Gene Conversions Are Insensitive to Interference and the Centromere Effect
Danny E Miller, Clarissa B Smith, Nazanin Yeganeh Kazemi, et al.
G3 (Bethesda, Md.)
|
September 25, 2020
Identification and Characterization of Breakpoints and Mutations on <i>Drosophila melanogaster</i> Balancer Chromosomes
Danny E Miller, Lily Kahsai, Kasun Buddika, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2023
Subdural hemorrhage, macrocephaly, rash, and developmental delay in an infant: A pathogenic variant in NLRP3 causes CINCA/NOMID
Ajay S Koti, Aviya Lanis, Samuel Finlayson, et al.
The Journal of Molecular Diagnostics : JMD
|
January 5, 2025
Concordance of Whole-Genome Long-Read Sequencing with Standard Clinical Testing for Prader-Willi and Angelman Syndromes
Cate R Paschal, Miranda P G Zalusky, Anita E Beck, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2018
Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance
Kelly L Jones, Erin A McNamara, Mauro Longoni, et al.
Biorxiv : the Preprint Server for Biology
|
July 2, 2026
Determinants of haplotype phasing accuracy in long-read human genome sequencing
Nikhita Damaraju, F Graeme Frost, Jiayu Fu, et al.
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Search research articles
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Showing results (41-50 of 112) with videos related to
Sort By:
Page
of 12
Maternal Health, Neonatology and Perinatology
|
March 16, 2023
Congenital pleuropulmonary blastoma in a newborn with a variant of uncertain significance in DICER1 evaluated by RNA-sequencing
Allison N J Lyle, Timothy J D Ohlsen, Danny E Miller, et al.
G3 (Bethesda, Md.)
|
October 27, 2015
Dynamics of Wolbachia pipientis Gene Expression Across the Drosophila melanogaster Life Cycle
Florence Gutzwiller, Catarina R Carmo, Danny E Miller, et al.
Maternal Health, Neonatology and Perinatology
|
May 25, 2023
Correction to: Congenital pleuropulmonary blastoma in a newborn with a variant of uncertain significance in DICER1 evaluated by RNA-sequencing
Allison N J Lyle, Timothy J D Ohlsen, Danny E Miller, et al.
Nucleic Acids Research
|
July 17, 2025
Splice-modulating antisense oligonucleotides targeting a pathogenic intronic variant in adult polyglucosan body disease correct mis-splicing and restore enzyme activity in patient cells
Ria Thomas, Emily Miyoshi, Hasan O Akman, et al.
Genetics
|
March 6, 2016
Whole-Genome Analysis of Individual Meiotic Events in Drosophila melanogaster Reveals That Noncrossover Gene Conversions Are Insensitive to Interference and the Centromere Effect
Danny E Miller, Clarissa B Smith, Nazanin Yeganeh Kazemi, et al.
G3 (Bethesda, Md.)
|
September 25, 2020
Identification and Characterization of Breakpoints and Mutations on <i>Drosophila melanogaster</i> Balancer Chromosomes
Danny E Miller, Lily Kahsai, Kasun Buddika, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2023
Subdural hemorrhage, macrocephaly, rash, and developmental delay in an infant: A pathogenic variant in NLRP3 causes CINCA/NOMID
Ajay S Koti, Aviya Lanis, Samuel Finlayson, et al.
The Journal of Molecular Diagnostics : JMD
|
January 5, 2025
Concordance of Whole-Genome Long-Read Sequencing with Standard Clinical Testing for Prader-Willi and Angelman Syndromes
Cate R Paschal, Miranda P G Zalusky, Anita E Beck, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2018
Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance
Kelly L Jones, Erin A McNamara, Mauro Longoni, et al.
Biorxiv : the Preprint Server for Biology
|
July 2, 2026
Determinants of haplotype phasing accuracy in long-read human genome sequencing
Nikhita Damaraju, F Graeme Frost, Jiayu Fu, et al.
Page
of 12