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Showing 51–66 of 66 results

Advanced filters: Author: Scott Papp Clear advanced filters

Towards integrated photonic interposers for processing octave-spanning microresonator frequency combs

Key steps towards photonic interposers for integrated optical synthesizers are shown: filters, mixers, linear processing of an octave-spanning microcomb, integration of microcomb and interposer layers, and a system-level feasibility analysis.

Ashutosh Rao
Gregory Moille
Kartik Srinivasan
ResearchOpen Access26 May 2021
Light: Science & Applications

Volume: 10, P: 1-13
SMARCB1 protein and mRNA loss is not caused by promoter and histone hypermethylation in epithelioid sarcoma

Gergő Papp
Yi-Che Changchien
Zoltán Sápi
Research23 Nov 2012
Modern Pathology

Volume: 26, P: 393-403
Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

Marie Morimoto
Vikas Bhambhani
May Christine V. Malicdan
ResearchOpen Access10 Feb 2023
npj Genomic Medicine

Volume: 8, P: 1-16
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Lance H. Rodan
Rebecca C. Spillmann
Vandana Shashi
Research23 Jun 2021
Genetics in Medicine

Volume: 23, P: 1922-1932
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Felix Marbach
Georgi Stoyanov
Christian P. Schaaf
ResearchOpen Access08 Apr 2021
Genetics in Medicine

Volume: 23, P: 1465-1473
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Thomas A. Ravenscroft
Jennifer B. Phillips
Hugo J. Bellen
Research10 Jun 2021
Genetics in Medicine

Volume: 23, P: 1889-1900
Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Shilpa Nadimpalli Kobren
Dustin Baldridge
Isaac S. Kohane
ResearchOpen Access12 Feb 2021
Genetics in Medicine

Volume: 23, P: 1075-1085
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Sacha Ferdinandusse
Kirsty McWalter
Frédéric M. Vaz
ResearchOpen Access26 Nov 2020
Genetics in Medicine

Volume: 23, P: 740-750
Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Kelly Schoch
Cecilia Esteves
Vandana Shashi
Research23 Oct 2020
Genetics in Medicine

Volume: 23, P: 259-271
Social and moral psychology of COVID-19 across 69 countries

Flavio Azevedo
Tomislav Pavlović
Waldir M. Sampaio
ResearchOpen Access11 May 2023
Scientific Data

Volume: 10, P: 1-26
A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases

Jennifer E. Kyle
Kelly G. Stratton
Thomas O. Metz
ResearchOpen Access21 Apr 2021
Scientific Data

Volume: 8, P: 1-12
A multi-modal data resource for investigating topographic heterogeneity in patient-derived xenograft tumors

Satwik Rajaram
Maike A. Roth
Lani F. Wu
ResearchOpen Access31 Oct 2019
Scientific Data

Volume: 6, P: 1-13
One is the loneliest number: genotypic matchmaking using the electronic health record

Elly Brokamp
Mary E. Koziura
Jimann Shin
Comments & Opinion06 Jul 2021
Genetics in Medicine

Volume: 23, P: 1830-1832
Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Lance H. Rodan
Rebecca C. Spillmann
Vandana Shashi
Amendments and Corrections14 Sept 2021
Genetics in Medicine

Volume: 23, P: 2016
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Sacha Ferdinandusse
Kirsty McWalter
Frédéric M. Vaz
Amendments and CorrectionsOpen Access19 Oct 2021
Genetics in Medicine

Volume: 23, P: 2467
Prostate cancer outcomes among older men: insurance status comparisons results from CaPSURE database

N Sadetsky
E P Elkin
P R Carroll
Research25 Sept 2007
Prostate Cancer and Prostatic Diseases

Volume: 11, P: 280-287

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Towards integrated photonic interposers for processing octave-spanning microresonator frequency combs

SMARCB1 protein and mRNA loss is not caused by promoter and histone hypermethylation in epithelioid sarcoma

Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Social and moral psychology of COVID-19 across 69 countries

A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases

A multi-modal data resource for investigating topographic heterogeneity in patient-derived xenograft tumors

One is the loneliest number: genotypic matchmaking using the electronic health record

Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Prostate cancer outcomes among older men: insurance status comparisons results from CaPSURE database

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