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Savatt, Juliann M
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1

PO-01-060 ARRHYTHMIA BURDEN AND DISTRIBUTION ACROSS THE TTN..:

Kelly, Melissa A. ; Savatt, Juliann M. ; Haggerty, Christopher...
Heart Rhythm.  21 (2024)  5 - p. S194-S195 , 2024
Link: https://doi.org/10.1016/..
 
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2

Clinical variants paired with phenotype: A rich resource fo..:

Chopra, Maya ; Savatt, Juliann M. ; Bingaman, Taylor I....
Genetics in Medicine.  26 (2024)  3 - p. 101035 , 2024
Link: https://doi.org/10.1016/..
 
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3

The Brain Gene Registry: a data snapshot:

Baldridge, Dustin ; Kaster, Levi ; Sancimino, Catherine...
Journal of Neurodevelopmental Disorders.  16 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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4

Expansion of the Genotypic and Phenotypic Spectrum of ASH1L..:

Cordova, Ineke ; Blesson, Alyssa ; Savatt, Juliann M....
Genes.  15 (2024)  4 - p. 423 , 2024
Link: https://doi.org/10.3390/..
 
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5

MSL2 variants lead to a neurodevelopmental syndrome with la..:

Karayol, Remzi ; Borroto, Maria Carla ; Haghshenas, Sadegheh...
The American Journal of Human Genetics.  111 (2024)  7 - p. 1330-1351 , 2024
Link: https://doi.org/10.1016/..
 
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6

Low adenoma burden in unselected patients with a pathogenic..:

Schwiter, Rachel ; Rocha, Heather ; Johns, Alicia...
Genetics in Medicine.  25 (2023)  12 - p. 100949 , 2023
Link: https://doi.org/10.1016/..
 
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7

Response to van Riel et al:

Savatt, Juliann M. ; Oetjens, Matthew T. ; Myers, Scott M..
Genetics in Medicine.  25 (2023)  1 - p. 161-163 , 2023
Link: https://doi.org/10.1016/..
 
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8

De novo variants of CSNK2B cause a new intellectual disabil..:

Asif, Maria ; Kaygusuz, Emrah ; Shinawi, Marwan...
Human Genetics and Genomics Advances.  3 (2022)  3 - p. 100111 , 2022
Link: https://doi.org/10.1016/..
 
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9

Clinical validity assessment of genes frequently tested on ..:

Riggs, Erin Rooney ; Bingaman, Taylor I. ; Barry, Carrie-Ann...
Genetics in Medicine.  24 (2022)  9 - p. 1899-1908 , 2022
Link: https://doi.org/10.1016/..
 
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10

Observational study of population genomic screening for var..:

Savatt, Juliann M. ; Ortiz, Nicole M. ; Thone, Gretchen M....
BMC Medicine.  20 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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11

Clinical validation of genomic functional screen data: Anal..:

Schiabor Barrett, Kelly M. ; Masnick, Max ; Hatchell, Kathryn E....
Human Genetics and Genomics Advances.  3 (2022)  2 - p. 100086 , 2022
Link: https://doi.org/10.1016/..
 
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12

A RE-AIM Framework Analysis of DNA-Based Population Screeni..:

Jones, Laney K. ; Strande, Natasha T. ; Calvo, Evan M....
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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13

Frequency of truncating FLCN variants and Birt-Hogg-Dubé–as..:

Savatt, Juliann M. ; Shimelis, Hermela ; Moreno-De-Luca, Andres...
Genetics in Medicine.  24 (2022)  9 - p. 1857-1866 , 2022
Link: https://doi.org/10.1016/..
 
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14

Application of a framework to guide genetic testing communi..:

Hallquist, Miranda L. G. ; Tricou, Eric P. ; Ormond, Kelly E....
Genome Medicine.  13 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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15

Genetic Testing in Neurodevelopmental Disorders:

Savatt, Juliann M. ; Myers, Scott M.
Frontiers in Pediatrics.  9 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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