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Author Details

Teresa N Sparks
University of California San Francisco
2009
70
18
PMIDPaper TitleJournal TitlePublished Year
38054560Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.Prenat Diagn2024
37594370The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction.Prenat Diagn2024
34874073Prenatal phenotype of 47, XXY (Klinefelter syndrome).Prenat Diagn2023
37752660Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.Prenat Diagn2023
37853803Optimal timing of delivery for growth restricted fetuses with gastroschisis: A decision analysis.Prenat Diagn2023
37872195Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.NPJ Genom Med2023
37236975Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.NPJ Genom Med2023
36588186A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy.Prenat Diagn2023
36603834Understanding Preterm Birth in Pregnancies Complicated by Nonimmune Hydrops Fetalis.Am J Perinatol2023
36308388Obstetrical and neonatal outcomes of cardio-facio-cutaneous syndrome: Prenatal consequences of Ras/MAPK dysregulation.Am J Med Genet A2023
36029833How to choose a test for prenatal genetic diagnosis: a practical overview.Am J Obstet Gynecol2023
34331894Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis.Am J Obstet Gynecol2022
35669190"Let's Just Wait Until She's Born": Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic Research.Front Genet2022
35396980Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach.Genet Med2022
35723972The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing.Prenat Diagn2022
36403095Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.Prenat Diagn2022
35872606Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology.Am J Med Genet C Semin Med Genet2022
36106778Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI-FDA Meeting).J Clin Pharmacol2022
35995366Cost-Effectiveness of Exome Sequencing versus Targeted Gene Panels for Prenatal Diagnosis of Fetal Effusions and Non-Immune Hydrops Fetalis.Am J Obstet Gynecol MFM2022
34942405Prenatal presentation of multiple anomalies associated with haploinsufficiency for ARID1A.Eur J Med Genet2022
35106791Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis.Prenat Diagn2022
34606761Response to "Further genetic testing in prenatal cases of nonimmune hydrops fetalis with a normal array: a targeted panel or exome?"Am J Obstet Gynecol2022
34057224Preference for secondary findings in prenatal and pediatric exome sequencing.Prenat Diagn2022
31327283Cell-free fetal DNA screening for detection of microdeletion syndromes: a cost-effectiveness analysis.J Matern Fetal Neonatal Med2021
33847422Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis.Ultrasound Obstet Gynecol2021
35280337Twin chorionicity and zygosity both vary with maternal age.Prenat Diagn2021
34453133Correction to: Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
34507800SMFM Fetal Anomalies Consult Series #4: Genitourinary anomalies.Am J Obstet Gynecol2021
34507799Hypospadias.Am J Obstet Gynecol2021
34560766The Current State and Future of Fetal Therapies.Clin Obstet Gynecol2021
34285390Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
34082169Interval growth across gestation in pregnancies with fetal gastroschisis.Am J Obstet Gynecol MFM2021
33321536Outcomes of Monochorionic, Diamniotic Twin Pregnancies with Prenatally Diagnosed Intertwin Weight Discordance.Am J Perinatol2021
32702189Variants of uncertain significance in prenatal microarrays: a retrospective cohort study.BJOG2021
33027564Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.N Engl J Med2020
31994743The utility of exome sequencing for fetal pleural effusions.Prenat Diagn2020
31981373Utility of chromosomal microarray for diagnosis in cases of nonimmune hydrops fetalis.Prenat Diagn2020
31679051Expanded carrier screening: counseling and considerations.Hum Genet2020
31652356The utility of nuchal translucency ultrasound in identifying rare chromosomal abnormalities not detectable by cell-free DNA screening.Prenat Diagn2020
28974133The growth-restricted fetus: risk of mortality by each additional week of expectant management.J Matern Fetal Neonatal Med2019
30199894Fetal Congenital Pulmonary Airway Malformation: The Role of an Objective Measurement of Cardiomediastinal Shift.Am J Perinatol2019
31087399A system-based approach to the genetic etiologies of non-immune hydrops fetalis.Prenat Diagn2019
30410095Nonimmune hydrops fetalis: identifying the underlying genetic etiology.Genet Med2019
29297200Utility of chromosomal microarray in anomalous fetuses.Prenat Diagn2018
30173949How should costs and cost-effectiveness be considered in prenatal genetic testing?Semin Perinatol2018
29528469Stage I Twin-Twin Transfusion Syndrome: Outcomes of Expectant Management and Prognostic Features.Am J Perinatol2018
29287298Polyhydramnios Affecting a Recipient-like Twin: Risk of Progression to Twin-Twin Transfusion Syndrome and Outcomes.Am J Perinatol2018
29304545Prenatal Diagnosis of Congenital Diaphragmatic Hernia: Does Laterality Predict Perinatal Outcomes?Am J Perinatol2018
29076544Non-Immune Hydrops Fetalis: Do Placentomegaly and Polyhydramnios Matter?J Ultrasound Med2018
27046743Hypertension in dichorionic twin gestations: how is birthweight affected?J Matern Fetal Neonatal Med2017
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Collaborators

Anne Slavotinek
Cincinnati Children's Hospital Medical Center
Co-authored papers 6
Ronald J Wapner
Columbia University
Co-authored papers 5
Kate Swanson
University of California san francisco
Co-authored papers 4
Sara L Ackerman
University of California San Francisco
Co-authored papers 3
Jessica Giordano
Columbia University Irving Medical Center
Co-authored papers 3
Barbara A Koenig
University of California-San Francisco.
Co-authored papers 3
Simon Outram
University of California-San Francisco.
Co-authored papers 3
Aleksandar Rajkovic
Co-authored papers 2
Shagun Aggarwal
Nizam's Institute of Medical Sciences
Co-authored papers 2
Pui-Yan Kwok
Cardiovascular Research Institute, University of California San Francisco
Co-authored papers 2
Andreas Dufke
Institute of Medical Genetics and Applied Genomics, University of Tuebingen
Co-authored papers 2
Lyn S Chitty
UCL Institute of Child Health and Great Ormond Street NHS Foundation Trust
Co-authored papers 2
Ferdinand Dhombres
Armand Trousseau Hospital, Sorbonne University
Co-authored papers 1
Sabrina Toro
University of Colorado Anschutz Medical Campus
Co-authored papers 1
Stephan J Sanders
Co-authored papers 1
Dominic J McMullan
Birmingham Women's and Children's NHS Foundation Trust
Co-authored papers 1
Michael H Duyzend
Massachusetts General Hospital
Co-authored papers 1
William A Weiss
University of California san francisco
Co-authored papers 1
Umber Agarwal
Liverpool Women's NHS Foundation Trust
Co-authored papers 1
Sophie Collardeau-Frachon
University Hospital of Lyon and Soffoet
Co-authored papers 1
Bimal P Chaudhari
Nationwide Children's Hospital
Co-authored papers 1
Raquel Gouveia Silva
Co-authored papers 1
Anjali J Kaimal
Massachusetts General Hospital
Co-authored papers 1
Jagadish Chandrabose Sundaramurthi
DOE Joint Genome Institute, Lawrence Berkeley National Laboratory
Co-authored papers 1
Nicole Vasilevsky
Critical Path Institute
Co-authored papers 1
Melissa A Haendel
Co-authored papers 1
David Valle
Johns Hopkins School of Medicine
Co-authored papers 1
R Alta Charo
University of Wisconsin-Madison/Nuclear Threat Initiative
Co-authored papers 1
Fowzan S Alkuraya
King Faisal Specialist Hospital and Research Center
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Eric J Huang
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Release 1.2