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/vufind/Search/Results?lookfor=%22Quiat%2C+Daniel%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Quiat%2C+Daniel%22&type=Person&sort=year
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PubPharm (19)
1
Genetic Diagnosis of Facioscapulohumeral Muscular Dystrophy Type 1 Using Rare Variant Linkage Analysis and Long Read Genome Sequencing
enthalten in:
bioRxiv.org
| 2024
von
Li, K.
|
Quiat, D.
|
She, F.
| +11
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2
Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation
enthalten in:
Circulation. Genomic and precision medicine
| 2023
von
Kim, Y.
|
Gunnarsdóttir, O.
|
Viveiros, A.
| +14
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3
Damaging variants in FOXI3 cause microtia and craniofacial microsomia
enthalten in:
Genetics in medicine : official journal of the American College of Medical Genetics
| 2023
von
Quiat, D.
|
Timberlake, A.
|
Curran, J.
| +23
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4
Population Prevalence of Premature Truncating Variants in Plakophilin-2 and Association With Arrhythmogenic Right Ventricular Cardiomyopathy : A UK Biobank Analysis
enthalten in:
Circulation. Genomic and precision medicine
| 2022
von
Hylind, R.
|
Pereira, A.
|
Quiat, D.
| +7
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5
An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations
enthalten in:
Proceedings of the National Academy of Sciences of the United States of America
| 2022
von
Quiat, D.
|
Kim, S.
|
Zhang, Q.
| +18
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6
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk
enthalten in:
American journal of human genetics
| 2022
von
Willcox, J.
|
Geiger, J.
|
Morton, S.
| +20
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7
Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity
enthalten in:
Circulation. Genomic and precision medicine
| 2022
von
Morton, S.
|
Pereira, A.
|
Quiat, D.
| +17
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8
Genomic frontiers in congenital heart disease
enthalten in:
Nature reviews. Cardiology
| 2022
von
Morton, S.
|
Quiat, D.
|
Seidman, J.
| +1
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9
Left Ventricular Outflow Tract Gradient Is Associated With Coronary Artery Obstruction in Children With Williams-Beuren Syndrome
enthalten in:
Journal of cardiothoracic and vascular anesthesia
| 2021
von
Tan, A.
|
Quiat, D.
|
Ghelani, S.
| +1
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10
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease
enthalten in:
JAMA cardiology
| 2021
von
Morton, S.
|
Shimamura, A.
|
Newburger, P.
| +20
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bioRxiv.org
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14
Research Support, N.I.H., Extramural
13
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2
MicroRNAs
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cardiomyopathies
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genetics
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Craniofacial microsomia
1
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1
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FOXI3
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Erscheinungszeitraum
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2020-
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2010-2019
2
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