Danielle LaGrave - Concepedia

Author

Danielle LaGrave

ARUP Laboratories (United States)

Also Known As

D. R. LaGrave, Danielle LaGrave, Danielle Lagrave

Publications

516

Citations

H-Index

Concepts

All Affiliations

ARUP Laboratories (United States)University of Utah

About

Danielle LaGrave is an author at ARUP Laboratories (United States) specializing in genetics, medicine, and autism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	167
2	Public Health	1	1	144
3	Medical Laboratory Science	1	1	144
4	Obstetrics	1	1	144
5	Autism	1	1	23

Danielle LaGrave

Publications

397

Citations

H-Index

Page 1

	Year	Citations
Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing Christine E. Miller, Patti Krautscheid, Erin E. Baldwin, American Journal of Medical Genetics Part A Genetic TestingGeneticsGenetic EpidemiologyGynecologyGenetic Counselor Review	2014	144
Practice Guidelines for Communicating a Prenatal or Postnatal Diagnosis of Down Syndrome: Recommendations of the National Society of Genetic Counselors Blythe G. Crissman, Cori Feist, Susan L. Sell, Journal of Genetic Counseling	2011	126
A cost‐effectiveness analysis of cell free DNA as a replacement for serum screening for Down syndrome Brandon S. Walker, Brian R. Jackson, Danielle LaGrave, Prenatal Diagnosis	2014	44
Chromosomal loss of 3q26.3‐3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability Alison Millson, Danielle LaGrave, Mary Willis, American Journal of Medical Genetics Part A	2011	27
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder Gifty Bhat, Danielle LaGrave, Alison Millson, European Journal of Medical Genetics MedicineGeneticsXq11.1-11.2 DeletionAutism Spectrum Disorder	2016	23
The impact of utilization of early aneuploidy screening on amniocenteses available for training in obstetrics and fetal medicine Nancy C. Rose, Danielle LaGrave, Brent Hafen, Prenatal Diagnosis	2013	17
Detection of maternal X chromosome abnormalities using single nucleotide polymorphism–based noninvasive prenatal testing Kimberly Martin, Carole Samango‐Sprouse, Valerie Kantor, American Journal of Obstetrics & Gynecology MFM	2020	16

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