Teresa N Sparks (Teresa Sparks, T N Sparks)

ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 34

Top Venues

Prenatal diagnosis

NPJ genomic medicine

The New England journal of medicine

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine

University of California San Francisco

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of California San Francisco Aug 01 2017

United States

Maternal-Fetal Medicine specialist and Clinical Geneticist :: Obstetrics, Gynecology, & Reproductive Sciences

Publications

Nuriye N Sahin Hodoglugil, Billie R Lianoglou, Sara Ackerman, Teresa N Sparks, Mary E Norton
Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US. Prenatal diagnosis (2023)
Harriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, Katie Tick, Julia E H Brown, Teresa N Sparks
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies. Prenatal diagnosis 44 (3) (2023)
Claire H Packer, Rachel A Pilliod, Aaron B Caughey, Teresa N Sparks
Optimal timing of delivery for growth restricted fetuses with gastroschisis: A decision analysis. Prenatal diagnosis (2023)
Harriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, Katie Tick, Julia E H Brown, Teresa N Sparks
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies. Prenatal diagnosis (2023)
Harriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, Katie Tick, Julia E H Brown, Teresa N Sparks
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies. Prenatal diagnosis 44 (3) (2023)
Matthew A Shear, Kate Swanson, Ria Garg, Angie C Jelin, John Boscardin, Mary E Norton, Teresa N Sparks
A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy. Prenatal diagnosis 43 (2) (2023)
Matthew A Shear, Kate Swanson, Ria Garg, Angie C Jelin, John Boscardin, Mary E Norton, Teresa N Sparks
A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy. Prenatal diagnosis 43 (2) (2023)
Harriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, Katie Tick, Julia E H Brown, Teresa N Sparks
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies. Prenatal diagnosis 44 (3) (2023)
Matthew A Shear, Kate Swanson, Ria Garg, Angie C Jelin, John Boscardin, Mary E Norton, Teresa N Sparks
A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy. Prenatal diagnosis (2023)
Bobby K Brar, Karin J Blakemore, Christine Hertenstein, Jena L Miller, Kristen A Miller, Hanan Shamseldin, Sateesh Maddirevula, Thomas Hays, Billie Lianoglou, Stephanie Dukhovny, Linda A Baker, Teresa N Sparks, Ronald Wapner, Fowzan S Alkuraya, Mary E Norton, Angie C Jelin, null null
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction. Prenatal diagnosis (2023)
Harriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, Katie Tick, Julia E H Brown, Teresa N Sparks
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies. Prenatal diagnosis 44 (3) (2023)
Leigh C Carmody, Michael A Gargano, Sabrina Toro, Nicole A Vasilevsky, Margaret P Adam, Hannah Blau, Lauren E Chan, David Gomez Andres, Rita Horvath, Megan L Kraus, Markus S Ladewig, David Lewis-Smith, Hanns Lochmüller, Nicolas A Matentzoglu, Monica C Munoz-Torres, Catharina Schuetz, Berthold Seitz, Morgan N Similuk, Teresa N Sparks, Timmy Strauß, Emilia M Swietlik, Rachel Thompson, Xingmin Aaron Zhang, Christopher John Mungall, Melissa A Haendel, Peter Nick Robinson
The Medical Action Ontology: A Tool for Annotating and Analyzing Treatments and Clinical Management of Human Disease. medRxiv : the preprint server for health sciences (2023)
Harriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, Katie Tick, Julia E H Brown, Teresa N Sparks
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies. Prenatal diagnosis 44 (3) (2023)
Matthew A Shear, Kate Swanson, Ria Garg, Angie C Jelin, John Boscardin, Mary E Norton, Teresa N Sparks
A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy. Prenatal diagnosis (2023)
Matthew A Shear, Kate Swanson, Ria Garg, Angie C Jelin, John Boscardin, Mary E Norton, Teresa N Sparks
A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy. Prenatal diagnosis 43 (2) (2023)
Gillian V Blayney, Eoghan Laffan, Preethi A Jacob, Caitlin D Baptiste, Heinz Gabriel, Teresa N Sparks, Yuval Yaron, Mary E Norton, Karin E M Diderich, Yiming Wang, Karen Chong, David Chitayat, Neelam Saini, Shagun Aggarwal, Montse Pauta, Antoni Borrell, Kelly Gilmore, Natalie Jane Chandler, Stephanie K Allen, Neeta L Vora, Abdul Noor, Caitriona Monaghan, Mark David Kilby, Ronald J Wapner, Lyn S Chitty, Fionnuala Mone
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis. Prenatal diagnosis (2023)
Anne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, Mark Kvale, Billie Lianoglou, Tiffany Yip, Hannah Hoban, Simon Outram, Beatrice Anguiano, Flavia Chen, Jeremy Michelson, Roberta M Cilio, Cynthia Curry, Renata C Gallagher, Marisa Gardner, Rachel Kuperman, Bryce Mendelsohn, Elliott Sherr, Joseph T C Shieh, Jonathan Strober, Allison Tam, Jessica Tenney, William Weiss, Amy Whittle, Garrett Chin, Amanda Faubel, Hannah Prasad, Yusuph Mavura, Jessica Van Ziffle, W Patrick Devine, Ugur Hodoglugil, Pierre-Marie Martin, Teresa N Sparks, Barbara Koenig, Sara Ackerman, Neil Risch, Pui-Yan Kwok, Mary E Norton
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ genomic medicine 8 (1) (2023)
Anne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, Mark Kvale, Billie Lianoglou, Tiffany Yip, Hannah Hoban, Simon Outram, Beatrice Anguiano, Flavia Chen, Jeremy Michelson, Roberta M Cilio, Cynthia Curry, Renata C Gallagher, Marisa Gardner, Rachel Kuperman, Bryce Mendelsohn, Elliott Sherr, Joseph T C Shieh, Jonathan Strober, Allison Tam, Jessica Tenney, William Weiss, Amy Whittle, Garrett Chin, Amanda Faubel, Hannah Prasad, Yusuph Mavura, Jessica Van Ziffle, W Patrick Devine, Ugur Hodoglugil, Pierre-Marie Martin, Teresa N Sparks, Barbara Koenig, Sara Ackerman, Neil Risch, Pui-Yan Kwok, Mary E Norton
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ genomic medicine 8 (1) (2023)
Bobby K Brar, Marisa Gilstrop Thompson, Neeta L Vora, Kelly Gilmore, Karin Blakemore, Kristen A Miller, Jessica L Giordano, Andreas Dufke, Beatrix Wong, Samantha Stover, Billie Lianoglou, Ignatia B Van den Veyver, Esther Dempsey, Mara Rosner, Karen Chong, David Chitayat, Teresa N Sparks, Mary E Norton, Ronald Wapner, Kristin Baranano, Angie C Jelin, null null
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series. Prenatal diagnosis (2022)
Kate Swanson, Mary E Norton, Billie R Lianoglou, Angie C Jelin, Ugur Hodoglugil, Jessica Van Ziffle, Patrick Devine, Teresa N Sparks
The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing. Prenatal diagnosis 42 (10) (2022)
Kate Swanson, Kelsey B Loeliger, Shilpa P Chetty, Teresa N Sparks, Mary E Norton
Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis. Prenatal diagnosis 42 (5) (2022)
Fionnuala Mone, R Y Eberhardt, M E Hurles, D J Mcmullan, E R Maher, J Lord, L S Chitty, E Dempsey, T Homfray, J L Giordano, R J Wapner, Lu-Ming Sun, Teresa N Sparks, M E Norton, Mark David Kilby
Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 58 (4) (2021)
Kate Swanson, Juliet C Bishop, Huda B Al-Kouatly, Mona Makhamreh, Thomas Felton, Neeta L Vora, Teresa N Sparks, Angie C Jelin
Prenatal phenotype of 47, XXY (Klinefelter syndrome). Prenatal diagnosis (2021)
Kate Swanson, Teresa N Sparks, Billie R Lianoglou, Flavia Chen, Sarah Downum, Sachi Patel, Shannon Rego, Tiffany Yip, Jessica Van Ziffle, Barbara A Koenig, Anne M Slavotinek, Mary E Norton
Preference for secondary findings in prenatal and pediatric exome sequencing. Prenatal diagnosis (2021)
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, Ilina D Pluym, Kerry Holliman, Jennifer Duffy, Sarah L Downum, Sachi Patel, Amanda Faubel, Nina M Boe, Nancy T Field, Aisling Murphy, Louise C Laurent, Jennifer Jolley, Cherry Uy, Anne M Slavotinek, Patrick Devine, Ugur Hodoglugil, Jessica Van Ziffle, Stephan J Sanders, Tippi C MacKenzie, Mary E Norton, null null, null null
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis. The New England journal of medicine 383 (18) (2020)
Anne H Mardy, A P Wiita, B V Wayman, K Drexler, Teresa N Sparks, M E Norton
Variants of uncertain significance in prenatal microarrays: a retrospective cohort study. BJOG : an international journal of obstetrics and gynaecology 128 (2) (2020)
Anne H Mardy, Naseem Rangwala, Yessenia Hernandez-Cruz, Kristen A Gosnell, Juan M Gonzalez, Mary E Norton, Teresa N Sparks
Utility of chromosomal microarray for diagnosis in cases of nonimmune hydrops fetalis. Prenatal diagnosis 40 (4) (2020)
Angie C Jelin, Nara Sobreira, Elizabeth Wohler, Benjamin Solomon, Teresa N Sparks, Katelynn G Sagaser, Katherine R Forster, Jena Miller, P Dane Witmer, Ada Hamosh, David Valle, Karin Blakemore
The utility of exome sequencing for fetal pleural effusions. Prenatal diagnosis 40 (5) (2020)
Teresa N Sparks
Expanded carrier screening: counseling and considerations. Human genetics 139 (9) (2019)
Anne H Mardy, Shilpa P Chetty, Mary E Norton, Teresa N Sparks
A system-based approach to the genetic etiologies of non-immune hydrops fetalis. Prenatal diagnosis 39 (9) (2019)
Victoria K Berger, Mary E Norton, Teresa N Sparks, Monica Flessel, Rebecca J Baer, Robert J Currier
The utility of nuchal translucency ultrasound in identifying rare chromosomal abnormalities not detectable by cell-free DNA screening. Prenatal diagnosis 40 (2) (2019)
Jacqueline G Parchem, Teresa N Sparks, Kristen Gosnell, Mary E Norton
Utility of chromosomal microarray in anomalous fetuses. Prenatal diagnosis 38 (2) (2018)
Victoria K Berger, Teresa N Sparks, Angie C Jelin, Chris Derderian, Cerine Jeanty, Kristen Gosnell, Tippi Mackenzie, Juan M Gonzalez
Non-Immune Hydrops Fetalis: Do Placentomegaly and Polyhydramnios Matter? Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine 37 (5) (2017)
Teresa N Sparks, Emily Griffin, Jessica Page, Rachel Pilliod, Brian L Shaffer, Aaron B Caughey
Down syndrome: perinatal mortality risks with each additional week of expectant management. Prenatal diagnosis 36 (4) (2016)

Teresa N Sparks.css-eqlu8i{font-size:small;padding-left:4px;} (Teresa Sparks, T N Sparks)

Publication Activity (10 Years)

Top Topics

Top Venues

Teresa N Sparks (Teresa Sparks, T N Sparks)