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Chitayat, David
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1

Associations and outcomes of prenatally detected rhombencep..:

Kunpalin, Yada ; Miller, Elka ; Raghuram, Kamini...
Prenatal Diagnosis.  , 2024
Link: https://doi.org/10.1002/..
 
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2

P812: Multiple fetal anomalies suggest a role for CDK20 in ..:

Chong, Karen ; Chitayat, David ; Ryan, Greg...
Genetics in Medicine Open.  2 (2024)  - p. 101720 , 2024
Link: https://doi.org/10.1016/..
 
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3

P769: Trio-whole exome and whole genome sequencing in fetal..:

Gershon, Ariel ; Anandampillai, Tanvi ; Arshad, Maahil...
Genetics in Medicine Open.  2 (2024)  - p. 101677 , 2024
Link: https://doi.org/10.1016/..
 
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4

Prenatal diagnosis of ROR‐2 related Robinow syndrome presen..:

Yang, Liying ; Shannon, Patrick ; Silver, Rachel...
Prenatal Diagnosis.  44 (2024)  5 - p. 653-656 , 2024
Link: https://doi.org/10.1002/..
 
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5

Validation of low‐pass genome sequencing for prenatal diagn..:

Mighton, Chloe ; Noor, Abdul ; Watkins, Nicholas...
Prenatal Diagnosis.  44 (2024)  4 - p. 443-453 , 2024
Link: https://doi.org/10.1002/..
 
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6

P610: Identification of trinucleotide repeat expansions in ..:

Guidugli, Lucia ; Hammer, Monia ; Cao, Bryant...
Genetics in Medicine Open.  2 (2024)  - p. 101516 , 2024
Link: https://doi.org/10.1016/..
 
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7

P866: Exploring the impact of secondary findings in a cohor..:

Fooks, Katharine ; Vermeer, Lydia ; Poole, Elise...
Genetics in Medicine Open.  2 (2024)  - p. 101780 , 2024
Link: https://doi.org/10.1016/..
 
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8

P531: Developing the patient-reported Genetic testing Utili..:

Poole, Elise ; Luca, Stephanie ; Assamad, Daniel...
Genetics in Medicine Open.  2 (2024)  - p. 101430 , 2024
Link: https://doi.org/10.1016/..
 
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9

Revisiting the Implications of a Wide or Narrow Fetal Cavum..:

Sichitiu, Joanna ; Ghannad‐Zadeh, Kimia ; Van Mieghem, Tim...
Journal of Ultrasound in Medicine.  43 (2024)  8 - p. 1461-1466 , 2024
Link: https://doi.org/10.1002/..
 
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10

P804: Prenatal diagnosis of atypical Holt-Oram syndrome cau..:

Mackley, Michael ; Silver, Rachel ; Watkins, Nicholas...
Genetics in Medicine Open.  2 (2024)  - p. 101712 , 2024
Link: https://doi.org/10.1016/..
 
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11

P782: Validation of low-pass genome sequencing for prenatal..:

Mighton, Chloe ; Noor, Abdul ; Watkins, Nicholas...
Genetics in Medicine Open.  2 (2024)  - p. 101690 , 2024
Link: https://doi.org/10.1016/..
 
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12

A metabolic signature for NADSYN1-dependent congenital NAD ..:

Szot, Justin O. ; Cuny, Hartmut ; Martin, Ella M.M.A....
Journal of Clinical Investigation.  134 (2024)  4 - p. , 2024
Link: https://doi.org/10.1172/..
 
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13

Expanding the phenotypic spectrum of NOTCH1 variants: clini..:

Stanley, Kaitlin J. ; Kalbfleisch, Kelsey J. ; Moran, Olivia M....
European Journal of Human Genetics.  32 (2024)  7 - p. 795-803 , 2024
Link: https://doi.org/10.1038/..
 
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14

169 Curating the fetal genome: experience of the ClinGen pr..:

Galloway, Stephanie ; Giordano, Jessica L. ; Thomas-Wilson, Amanda...
American Journal of Obstetrics and Gynecology.  230 (2024)  1 - p. S106 , 2024
Link: https://doi.org/10.1016/..
 
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15

De novo triplication at 1p36.23p36.22 further refines the d..:

Oh, Rachel Youjin ; Chun, Kathy ; Kowalski, Paul E..
American Journal of Medical Genetics Part A.  191 (2023)  6 - p. 1607-1613 , 2023
Link: https://doi.org/10.1002/..
 
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