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Azzariti, Danielle R.
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1

Seven years since the launch of the Matchmaker Exchange: Th..:

Boycott, Kym M. ; Azzariti, Danielle R. ; Hamosh, Ada.
Human Mutation.  , 2022
Link: https://doi.org/10.1002/..
 
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2

Recontacting registry participants with genetic updates thr..:

Savatt, Juliann M. ; Azzariti, Danielle R. ; Ledbetter, David H....
Genetics in Medicine.  23 (2021)  9 - p. 1738-1745 , 2021
Link: https://doi.org/10.1038/..
 
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3

Variant interpretation is a component of clinical practice ..:

Wain, Karen E. ; Azzariti, Danielle R. ; Goldstein, Jennifer L....
Genetics in Medicine.  22 (2020)  4 - p. 785-792 , 2020
Link: https://doi.org/10.1038/..
 
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4

A survey assessing adoption of the ACMG-AMP guidelines for ..:

Niehaus, Annie ; Azzariti, Danielle R. ; Harrison, Steven M....
Genetics in Medicine.  21 (2019)  8 - p. 1699-1701 , 2019
Link: https://doi.org/10.1038/..
 
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5

Development of Clinical Domain Working Groups for the Clini..:

Milko, Laura V. ; Funke, Birgit H. ; Hershberger, Ray E....
Genetics in Medicine.  21 (2019)  4 - p. 987-993 , 2019
Link: https://doi.org/10.1038/..
 
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6

Development of a consent resource for genomic data sharing ..:

Riggs, Erin Rooney ; Azzariti, Danielle R. ; Niehaus, Annie...
Genetics in Medicine.  21 (2019)  1 - p. 81-88 , 2019
Link: https://doi.org/10.1038/..
 
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7

Short-term costs of integrating whole-genome sequencing int..:

Christensen, Kurt D. ; Vassy, Jason L. ; Phillips, Kathryn A....
Genetics in Medicine.  20 (2018)  12 - p. 1544-1553 , 2018
Link: https://doi.org/10.1038/..
 
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8

ClinGen's GenomeConnect registry enables patient‐centered d..:

Savatt, Juliann M. ; Azzariti, Danielle R. ; Faucett, W. Andrew...
Human Mutation.  39 (2018)  11 - p. 1668-1676 , 2018
Link: https://doi.org/10.1002/..
 
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9

ClinGen Variant Curation Expert Panel experiences and stand..:

Rivera‐Muñoz, Edgar A. ; Milko, Laura V. ; Harrison, Steven M....
Human Mutation.  39 (2018)  11 - p. 1614-1622 , 2018
Link: https://doi.org/10.1002/..
 
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10

Approaches to carrier testing and results disclosure in tra..:

Porter, Kathryn M. ; Kauffman, Tia L. ; Koenig, Barbara A....
Molecular Genetics & Genomic Medicine.  6 (2018)  6 - p. 898-909 , 2018
Link: https://doi.org/10.1002/..
 
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11

Clinical laboratories collaborate to resolve differences in..:

Harrison, Steven M. ; Dolinsky, Jill S. ; Knight Johnson, Amy E....
Genetics in Medicine.  19 (2017)  10 - p. 1096-1104 , 2017
Link: https://doi.org/10.1038/..
 
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12

Determinants of white matter hyperintensity burden in patie..:

Rost, Natalia S. ; Cloonan, Lisa ; Kanakis, Allison S....
Neurology.  86 (2016)  20 - p. 1880-1886 , 2016
Link: https://doi.org/10.1212/..
 
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13

Using ClinVar as a Resource to Support Variant Interpretati..:

Harrison, Steven M. ; Riggs, Erin R. ; Maglott, Donna R....
Current Protocols in Human Genetics.  89 (2016)  1 - p. , 2016
Link: https://doi.org/10.1002/..
 
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14

GenomeConnect: Matchmaking Between Patients, Clinical Labor..:

Kirkpatrick, Brianne E. ; Riggs, Erin Rooney ; Azzariti, Danielle R....
Human Mutation.  36 (2015)  10 - p. 974-978 , 2015
Link: https://doi.org/10.1002/..
 
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15

The Matchmaker Exchange: A Platform for Rare Disease Gene D..:

Philippakis, Anthony A. ; Azzariti, Danielle R. ; Beltran, Sergi...
Human Mutation.  36 (2015)  10 - p. 915-921 , 2015
Link: https://doi.org/10.1002/..
 
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