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Showing 1–33 of 33 results

Advanced filters: Author: David C. Schedl Clear advanced filters

Isolation of histone genes from unfractionated sea urchin DNA by subculture cloning in E. coli

Laurence H. Kedes
Annie C. Y. Chang
Stanley N. Cohen
Research12 Jun 1975
Nature

Volume: 255, P: 533-538
Compressive Volumetric Light-Field Excitation

David C. Schedl
Oliver Bimber
ResearchOpen Access25 Oct 2017
Scientific Reports

Volume: 7, P: 1-9
Whole-genome sequencing and variant discovery in C. elegans

LaDeana W Hillier
Gabor T Marth
Elaine R Mardis
Research20 Jan 2008
Nature Methods

Volume: 5, P: 183-188
Phosphorylation of the Src substrate Sam68 by Cdc2 during mitosis

Ross J Resnick
Stephen J Taylor
David Shalloway
Research11 Sept 1997
Oncogene

Volume: 15, P: 1247-1253
Search and rescue with airborne optical sectioning

Autonomous drones can help find injured or missing people when a large or hard to traverse area has to be searched, but their view can be obscured in dense forests. David Schedl and colleagues have developed a method to reveal humans in thermal imaging recordings, even in the presence of dense foliage.

David C. Schedl
Indrajit Kurmi
Oliver Bimber
Research23 Nov 2020
Nature Machine Intelligence

Volume: 2, P: 783-790
Longevity in Caenorhabditis elegans reduced by mating but not gamete production

David Gems
Donald L. Riddle
Research22 Feb 1996
Nature

Volume: 379, P: 723-725
Uptake of Escherichia coli DNA into HeLa cells enhanced by amphotericin B

B. VIJAYA KUMAR
GERALD MEDOFF
DAVID SCHLESSINGER
Research26 Jul 1974
Nature

Volume: 250, P: 323-325
A conserved RNA-binding protein controls germline stem cells in Caenorhabditis elegans

Sarah L. Crittenden
David S. Bernstein
Judith Kimble
Research22 May 2002
Nature

Volume: 417, P: 660-663
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Using well-calibrated statistical methods the authors jointly analyze Undiagnosed Diseases Network genomes, identifying known and novel disease genes. Software is publicly available to support future cross-cohort rare disease discovery efforts.

Shilpa Nadimpalli Kobren
Mikhail A. Moldovan
Shamil R. Sunyaev
ResearchOpen Access07 Aug 2025
Nature Communications

Volume: 16, P: 1-19
Improved limits on small-scale anisotropy in cosmic microwave background

Juan M. Uson
David T. Wilkinson
Research29 Nov 1984
Nature

Volume: 312, P: 427-429
A systematic map of direction preference in primary visual cortex

Michael Weliky
William H. Bosking
David Fitzpatrick
Research22 Feb 1996
Nature

Volume: 379, P: 725-728
Engineering the Caenorhabditis elegans genome using Cas9-triggered homologous recombination

CRISPR-Cas9–mediated cleavage is used to stimulate homologous recombination at specific target sites in the C. elegans genome, permitting flexible tagging and sequence modification of endogenous worm genes.

Daniel J Dickinson
Jordan D Ward
Bob Goldstein
Research01 Sept 2013
Nature Methods

Volume: 10, P: 1028-1034
The Identification and the Excretion Pattern of Isovaleryl Glucuronide in the Urine of Patients with Isovaleric Acidemia

David G Hine
Kay Tanaka
Research01 Jun 1984
Pediatric Research

Volume: 18, P: 508-512
Franklin flies again

David Jones
News & Views01 Sept 1988
Nature

Volume: 335, P: 18
Volumetric Light-Field Excitation

David C. Schedl
Oliver Bimber
ResearchOpen Access01 Jul 2016
Scientific Reports

Volume: 6, P: 1-9
Mitochondrial DNA gets the drift

David A. Clayton
News & Views01 Oct 1996
Nature Genetics

Volume: 14, P: 123-125
Hydrogen Peroxide Hemolysis: A Test for Biliary Obstruction

Bertram H Lubin
Robert L Baehner
Charles A Janeway
Research01 Sept 1970
Pediatric Research

Volume: 4, P: 476-477
Airborne Optical Sectioning for Nesting Observation

David C. Schedl
Indrajit Kurmi
Oliver Bimber
ResearchOpen Access29 Apr 2020
Scientific Reports

Volume: 10, P: 1-7
Cultural Divergence in popular music: the increasing diversity of music consumption on Spotify across countries

Pablo Bello
David Garcia
ResearchOpen Access27 Jul 2021
Humanities and Social Sciences Communications

Volume: 8, P: 1-8
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
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
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
tr-kit promotes the formation of a multimolecular complex composed by Fyn, PLCγ1 and Sam68

Maria Paola Paronetto
Julian P Venables
Claudio Sette
Research27 Nov 2003
Oncogene

Volume: 22, P: 8707-8715
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
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
Combined person classification with airborne optical sectioning

Indrajit Kurmi
David C. Schedl
Oliver Bimber
ResearchOpen Access09 Mar 2022
Scientific Reports

Volume: 12, P: 1-11
Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses

Kelly Schoch
Queenie K.-G. Tan
Vandana Shashi
Research05 May 2020
Genetics in Medicine

Volume: 22, P: 1269-1275
Regulation of hematopoietic stem cell growth

E C Attar
D T Scadden
Reviews30 Sept 2004
Leukemia

Volume: 18, P: 1760-1768
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
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

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Isolation of histone genes from unfractionated sea urchin DNA by subculture cloning in E. coli

Compressive Volumetric Light-Field Excitation

Whole-genome sequencing and variant discovery in C. elegans

Phosphorylation of the Src substrate Sam68 by Cdc2 during mitosis

Search and rescue with airborne optical sectioning

Longevity in Caenorhabditis elegans reduced by mating but not gamete production

Uptake of Escherichia coli DNA into HeLa cells enhanced by amphotericin B

A conserved RNA-binding protein controls germline stem cells in Caenorhabditis elegans

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Improved limits on small-scale anisotropy in cosmic microwave background

A systematic map of direction preference in primary visual cortex

Engineering the Caenorhabditis elegans genome using Cas9-triggered homologous recombination

The Identification and the Excretion Pattern of Isovaleryl Glucuronide in the Urine of Patients with Isovaleric Acidemia

Franklin flies again

Volumetric Light-Field Excitation

Mitochondrial DNA gets the drift

Hydrogen Peroxide Hemolysis: A Test for Biliary Obstruction

Airborne Optical Sectioning for Nesting Observation

Cultural Divergence in popular music: the increasing diversity of music consumption on Spotify across countries

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

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

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

tr-kit promotes the formation of a multimolecular complex composed by Fyn, PLCγ1 and Sam68

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

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

Combined person classification with airborne optical sectioning

Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses

Regulation of hematopoietic stem cell growth

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

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

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

Search

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