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Kinetic inductance traveling-wave amplifiers for multiplexed qubit readout

Applied physics letters, 2018-12, Vol.113 (24)

2018

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Frequency comb generation in superconducting resonators

Physical review letters, 2014-10, Vol.113 (18), p.187002-187002, Article 187002

2014

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Association Between Osteosarcoma and Deleterious Mutations in the RECQL4 Gene in Rothmund–Thomson Syndrome

JNCI : Journal of the National Cancer Institute, 2003-05, Vol.95 (9), p.669-674

2003

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Low-noise kinetic inductance traveling-wave amplifier using three-wave mixing

Applied physics letters, 2016-01, Vol.108 (1)

2016

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Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange

Journal of medical genetics, 2009-09, Vol.46 (9), p.626-634

2009

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Theory of multiwave mixing within the superconducting kinetic-inductance traveling-wave amplifier

Physical review. B, 2017-03, Vol.95 (10), p.104506, Article 104506

2017

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X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations

Clinical genetics, 2013-04, Vol.83 (4), p.352-358

2013

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Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations

Journal of medical genetics, 2001-11, Vol.38 (11), p.761-766

2001

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A marked paucity of granule cells in the developing cerebellum of the Npc1−/− mouse is corrected by a single injection of hydroxypropyl-β-cyclodextrin

Neurobiology of disease, 2014-10, Vol.70, p.117-126

2014

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A model of magnetic impurities within the Josephson junction of a phase qubit

Superconductor science & technology, 2010-02, Vol.23 (2), p.025026-025026

2010

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Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery

Lymphology, 2021, Vol.54 (4), p.167

2021

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The Absence of Mitochondrial Thioredoxin 2 Causes Massive Apoptosis, Exencephaly, and Early Embryonic Lethality in Homozygous Mice

Molecular and Cellular Biology, 2003-02, Vol.23 (3), p.916-922

2003

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Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistance

Molecular psychiatry, 2005-11, Vol.10 (11), p.976-977

2005

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Next generation sequencing is here now

Lymphology, 2014-12, Vol.47 (4), p.196-197

Erickson, R P

2014

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Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation

Lymphology, 2021, Vol.54 (2), p.78

2021

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Towards smaller and faster gas chromatography–mass spectrometry systems for field chemical detection

Journal of Chromatography A, 2005-03, Vol.1067 (1), p.285-294

2005

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Pharmacological and genetic modifications of somatic cholesterol do not substantially alter the course of CNS disease in Niemann–Pick C mice

Journal of inherited metabolic disease, 2000-02, Vol.23 (1), p.54-62

2000

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Neural responses to bitter compounds in rats

Brain research, 1997-05, Vol.756 (1), p.22-34

1997

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A Polymorphism in the 5' Flanking Region of the CD14 Gene Is Associated with Circulating Soluble CD14 Levels and with Total Serum Immunoglobulin E

American journal of respiratory cell and molecular biology, 1999-05, Vol.20 (5), p.976-983

1999

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Massively parallel DNA sequencing and the new approach to mutation detection: a step towards a lymphedema fine panel

Lymphology, 2012-03, Vol.45 (1), p.1-2

Erickson, R P

2012

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The evolution of neural coding ideas in the chemical senses

Physiology & behavior, 2000-04, Vol.69 (1), p.3-13

Erickson, Robert P

2000

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Mutations in FOXC2 ( MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

American journal of human genetics, 2000-12, Vol.67 (6), p.1382-1388

2000

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Transcription of the Sex-Determining Region Genes Sry and Zfy in the Mouse Preimplantation Embryo

Proceedings of the National Academy of Sciences - PNAS, 1993-02, Vol.90 (3), p.814-817

1993

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Modulation of rat chorda tympani nerve activity by lingual nerve stimulation

Journal of neurophysiology, 1995-04, Vol.73 (4), p.1468-1483

1995

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Linkage of circulating eosinophils to markers on chromosome 5q

American journal of respiratory and critical care medicine, 1998-12, Vol.158 (6), p.1739-1744

1998

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Kinetic inductance traveling-wave amplifiers for multiplexed qubit readout

Frequency comb generation in superconducting resonators

Association Between Osteosarcoma and Deleterious Mutations in the RECQL4 Gene in Rothmund–Thomson Syndrome

Low-noise kinetic inductance traveling-wave amplifier using three-wave mixing

Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange

Theory of multiwave mixing within the superconducting kinetic-inductance traveling-wave amplifier

X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations

Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations

A marked paucity of granule cells in the developing cerebellum of the Npc1−/− mouse is corrected by a single injection of hydroxypropyl-β-cyclodextrin

A model of magnetic impurities within the Josephson junction of a phase qubit

Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery

The Absence of Mitochondrial Thioredoxin 2 Causes Massive Apoptosis, Exencephaly, and Early Embryonic Lethality in Homozygous Mice

Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistance

Next generation sequencing is here now

Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation

Towards smaller and faster gas chromatography–mass spectrometry systems for field chemical detection

Pharmacological and genetic modifications of somatic cholesterol do not substantially alter the course of CNS disease in Niemann–Pick C mice

Neural responses to bitter compounds in rats

A Polymorphism in the 5' Flanking Region of the CD14 Gene Is Associated with Circulating Soluble CD14 Levels and with Total Serum Immunoglobulin E

Massively parallel DNA sequencing and the new approach to mutation detection: a step towards a lymphedema fine panel

The evolution of neural coding ideas in the chemical senses

Mutations in FOXC2 ( MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Transcription of the Sex-Determining Region Genes Sry and Zfy in the Mouse Preimplantation Embryo

Modulation of rat chorda tympani nerve activity by lingual nerve stimulation

Linkage of circulating eosinophils to markers on chromosome 5q

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