Teresa Sparks, MD, MAS

Title(s)Associate Professor, Ob/Gyn, Reproductive Sciences
SchoolSchool of Medicine
ORCID ORCID Icon0000-0002-8593-2186 Additional info
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    Collapse Biography 
    Collapse Education and Training
    University of California, San Francisco, San FranciscoMD2009 Medicine
    Brigham & Women's Hospital/Massachusetts General Hospital, BostonResidency2013Obstetrics & Gynecology
    University of California, San Francisco, San FranciscoFellowship2017Maternal Fetal Medicine and Clinical Genetics
    University of California, San Francisco, San FranciscoMAS2019Clinical Research
    Collapse Awards and Honors
    UCSF2008Genentech Research Fellowship
    UCSF2009Dean's Scholarship for Research
    UCSF2009MD with Distinction (MD with Thesis)
    Harvard Medical School2011Outstanding Medical Student Teacher
    UCSF2015Outstanding Resident Teacher
    UCSF2016Outstanding Resident Teacher
    UCSF2017Outstanding Resident Teacher
    Perinatal Research Society2018Abbott Nutrition/National Institutes of Health/Perinatal Research Society Early Career Speaker award
    UCSF2018Outstanding Resident Teacher
    Society for Maternal-Fetal Medicine2020Dru Carlson Memorial Award for best research in Ultrasound and Genetics
    UCSF2020Outstanding Resident Teacher
    American Society for Clinical Investigation20222022 Young Physician Scientist Award
    UCSF2022Outstanding Research Mentor Award
    UCSF2022Maternal-Fetal Medicine Fellowship Faculty Teaching Award
    UCSF2023Outstanding Research Mentor Award
    UCSF2023Maternal-Fetal Medicine Fellowship Faculty Teaching Award
    UCSF2024Exceptional Research Mentor Award
    UCSF2024MFM Fellow Award for Excellence in Didactic Teaching at UCSF

    Collapse Overview 
    Collapse Overview
    I am a physician who specializes in both Maternal-Fetal Medicine and Clinical Genetics. I care for individuals primarily through the Prenatal Diagnosis Center and the Fetal Treatment Center who are pregnant or considering pregnancy, particularly those that are higher risk for a variety of reasons. These reasons may include fetal birth defects, fetal genetic diseases, maternal genetic or non-genetic diseases, and many others. I am also Program Director for the Maternal-Fetal Medicine Fellowship at UCSF, and serve as Medical Director for the Prenatal Diagnosis Center at UCSF Benioff Children's Physicians (UBCP). In my role as a physician scientist, I am a Chan Zuckerberg Biohub Investigator as well as an Investigator for the UCSF Center for Maternal-Fetal Precision Medicine, Co-Director of the Women's Reproductive Health Research (WRHR)/K12 Program at UCSF, and serve as the alternate PI for the Maternal-Fetal Medicine Units (MFMU) Network award at UCSF. My research program is focused on developing a precision-based approach to care for non-immune hydrops fetalis (NIHF) and other fetal anomalies by establishing multicenter NIHF data over many years, performing genomic sequencing and other testing to discover the breadth of underlying causes, refining clinical testing algorithms, and developing novel in utero treatment approaches.

    Collapse Research 
    Collapse Research Activities and Funding
    Maternal Fetal Medicine Units Network: University of California, San Francisco
    NIH/NICHD 1UG1HD112092Mar 10, 2023 - Mar 9, 2030
    Role: Alternate PI at UCSF
    Chan Zuckerberg Biohub Investigator Program Mar 1, 2022 - Feb 28, 2027
    Role: PI
    NIH/NICHD R01HD107190Feb 11, 2022 - Feb 10, 2027
    Role: PI
    Doris Duke Charitable FoundationJul 1, 2021 - Jun 30, 2024
    Role: PI
    Women's Reproductive Health Research (WRHR) Program
    NIH/NICHD K12HD001262Jul 1, 2020 - Jun 30, 2025
    Role: Program Co-Director
    NICHD/NIH 5K12 HD001262Aug 1, 2017 - Jun 30, 2022
    Description: Women's Reproductive Health Research (WRHR) scholar

    Collapse ORNG Applications 
    Collapse Clinical Trials
    Collapse Featured Publications

    Collapse Featured Content 
    Collapse Featured Presentations

      Collapse Bibliographic 
      Collapse Publications
      Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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      Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
      1. Prenatal Exome Sequencing Identifies Dual Maternal-Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia. Prenat Diagn. 2025 Jan 02. Shear MA, Lianoglou B, Hodoglugil U, Devine WP, Lal A, Gonzalez J, Sparks TN. PMID: 39746815.
        View in: PubMed   Mentions:    Fields:    
      2. Fetal Intracranial Hemorrhage due to Uniparental Disomy and Unmasked MPL-Related Congenital Amegakaryocytic Thrombocytopenia. Prenat Diagn. 2024 Dec 31. Gano D, Glenn OA, Rand L, Heraty K, Devine P, Norton ME, Sparks TN. PMID: 39739357.
        View in: PubMed   Mentions:    Fields:    
      3. Prenatal exome sequencing for the structurally normal fetus: ready or not? Am J Obstet Gynecol MFM. 2025 Feb; 7(2):101513. Sparks TN. PMID: 39741061.
        View in: PubMed   Mentions:    Fields:    
      4. Fetal imaging, phenotyping, and genomic testing in modern prenatal diagnosis. Best Pract Res Clin Obstet Gynaecol. 2025 Feb; 98:102575. Shear MA, Robinson PN, Sparks TN. PMID: 39740319.
        View in: PubMed   Mentions:    Fields:    
      5. Fetal Brain MRI Findings in Myotonic Dystrophy and Considerations for Prenatal Genetic Testing. Neurol Genet. 2024 Dec; 10(6):e200171. Shear MA, Penon-Portmann M, Shieh JT, Glenn OA, Thiet MP, Chetty S, Sparks TN, Gano D. PMID: 39444647; PMCID: PMC11498903.
        View in: PubMed   Mentions:
      6. Updates in Prevention, Detection, and Management of Alloimmunized Pregnancies. Obstet Gynecol. 2024 Oct 01; 144(4):433-435. Sparks TN, Gray KJ. PMID: 39441955.
        View in: PubMed   Mentions:    Fields:    
      7. Patient understanding of prenatal exome sequencing. Am J Obstet Gynecol MFM. 2024 Nov; 6(11):101490. Swanson K, Norton ME, Ackerman SL, Lianoglou BR, Sahin-Hodoglugil NN, Sparks TN. PMID: 39270841.
        View in: PubMed   Mentions:    Fields:    
      8. Unusual Maternal and Fetal Findings With Cell-Free DNA Screening. Obstet Gynecol Surv. 2024 Sep; 79(9):539-546. Santoli CMA, Anastasio MK, Sparks TN, Dotters-Katz SK, Kuller JA. PMID: 39288158.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      9. Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter study. Am J Obstet Gynecol. 2024 Jun 22. Zemet R, Maktabi MA, Tinfow A, Giordano JL, Heisler TM, Yan Q, Plaschkes R, Stokes J, Walsh JM, Corcoran S, Schindewolf E, Miller K, Talati AN, Miller KA, Blakemore K, Swanson K, Ramm J, Bedei I, Sparks TN, Jelin AC, Vora NL, Gebb JS, Crosby DA, Berkenstadt M, Weisz B, Wapner RJ, Van Den Veyver IB. PMID: 38914189; PMCID: PMC11663227.
        View in: PubMed   Mentions: 1     Fields:    
      10. Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies. Prenat Diagn. 2024 03; 44(3):263-269. Rothschild HT, Lianoglou BR, Sahin Hodoglugil NN, Tick K, Brown JEH, Sparks TN. PMID: 38158591; PMCID: PMC10947859.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      11. Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis. Prenat Diagn. 2024 04; 44(4):422-431. Blayney GV, Laffan E, Jacob PA, Baptiste CD, Gabriel H, Sparks TN, Yaron Y, Norton ME, Diderich K, Wang Y, Chong K, Chitayat D, Saini N, Aggarwal S, Pauta M, Borrell A, Gilmore K, Chandler NJ, Allen S, Vora N, Noor A, Monaghan C, Kilby MD, Wapner RJ, Chitty LS, Mone F. PMID: 38054560; PMCID: PMC11044826.
        View in: PubMed   Mentions: 2     Fields:    Translation:Humans
      12. The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human disease. Med. 2023 Dec 08; 4(12):913-927.e3. Carmody LC, Gargano MA, Toro S, Vasilevsky NA, Adam MP, Blau H, Chan LE, Gomez-Andres D, Horvath R, Kraus ML, Ladewig MS, Lewis-Smith D, Lochmüller H, Matentzoglu NA, Munoz-Torres MC, Schuetz C, Seitz B, Similuk MN, Sparks TN, Strauss T, Swietlik EM, Thompson R, Zhang XA, Mungall CJ, Haendel MA, Robinson PN. PMID: 37963467; PMCID: PMC10842845.
        View in: PubMed   Mentions: 2     Fields:    Translation:Humans
      13. Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 Oct 23; 8(1):34. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37872195; PMCID: PMC10593851.
        View in: PubMed   Mentions:
      14. Optimal timing of delivery for growth restricted fetuses with gastroschisis: A decision analysis. Prenat Diagn. 2023 11; 43(12):1506-1513. Packer CH, Pilliod RA, Caughey AB, Sparks TN. PMID: 37853803.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      15. Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US. Prenat Diagn. 2023 10; 43(11):1394-1405. Sahin-Hodoglugil NN, Lianoglou BR, Ackerman S, Sparks TN, Norton ME. PMID: 37752660; PMCID: PMC10846391.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      16. The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction. Prenat Diagn. 2024 02; 44(2):196-204. Brar BK, Blakemore K, Hertenstein C, Miller JL, Miller KA, Shamseldin H, Maddirevula S, Hays T, Lianoglou B, Dukhovny S, Baker LA, Sparks TN, Wapner R, Alkuraya FS, Norton ME, Jelin AC, Fetal Sequencing Consortium. PMID: 37594370.
        View in: PubMed   Mentions: 1     Fields:    
      17. The Medical Action Ontology: A Tool for Annotating and Analyzing Treatments and Clinical Management of Human Disease. medRxiv. 2023 Jul 13. Carmody LC, Gargano MA, Toro S, Vasilevsky NA, Adam MP, Blau H, Chan LE, Gomez-Andres D, Horvath R, Kraus ML, Ladewig MS, Lewis-Smith D, Lochmüller H, Matentzoglu NA, Munoz-Torres MC, Schuetz C, Seitz B, Similuk MN, Sparks TN, Strauss T, Swietlik EM, Thompson R, Zhang XA, Mungall CJ, Haendel MA, Robinson PN. PMID: 37503136; PMCID: PMC10370244.
        View in: PubMed   Mentions:
      18. Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 May 26; 8(1):10. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37236975; PMCID: PMC10220040.
        View in: PubMed   Mentions: 11  
      19. A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy. Prenat Diagn. 2023 02; 43(2):133-143. Shear MA, Swanson K, Garg R, Jelin AC, Boscardin J, Norton ME, Sparks TN. PMID: 36588186; PMCID: PMC10268789.
        View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
      20. Understanding Preterm Birth in Pregnancies Complicated by Nonimmune Hydrops Fetalis. Am J Perinatol. 2023 07; 40(9):917-922. Swanson K, Norton ME, Downum SL, Gonzalez-Velez JM, Sparks TN. PMID: 36603834; PMCID: PMC10330491.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      21. Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series. Prenat Diagn. 2022 12; 42(13):1686-1693. Brar BK, Thompson MG, Vora NL, Gilmore K, Blakemore K, Miller KA, Giordano J, Dufke A, Wong B, Stover S, Lianoglou B, Van den Veyver I, Dempsey E, Rosner M, Chong K, Chitayat D, Sparks TN, Norton ME, Wapner R, Baranano K, Jelin AC, Fetal Sequencing Consortium. PMID: 36403095; PMCID: PMC9805891.
        View in: PubMed   Mentions: 1     Fields:    Translation:Humans
      22. Obstetrical and neonatal outcomes of cardio-facio-cutaneous syndrome: Prenatal consequences of Ras/MAPK dysregulation. Am J Med Genet A. 2023 02; 191(2):323-331. Jelin AC, Mahle A, Tran SH, Sparks TN, Rauen KA. PMID: 36308388; PMCID: PMC9839479.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      23. Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI-FDA Meeting). J Clin Pharmacol. 2022 09; 62 Suppl 1:S36-S52. Herzeg A, Almeida-Porada G, Charo RA, David AL, Gonzalez-Velez J, Gupta N, Lapteva L, Lianoglou B, Peranteau W, Porada C, Sanders SJ, Sparks TN, Stitelman DH, Struble E, Sumner CJ, MacKenzie TC. PMID: 36106778; PMCID: PMC9547535.
        View in: PubMed   Mentions: 5     Fields:    Translation:Humans
      24. How to choose a test for prenatal genetic diagnosis: a practical overview. Am J Obstet Gynecol. 2023 02; 228(2):178-186. Sparks TN, Dugoff L. PMID: 36029833; PMCID: PMC9877133.
        View in: PubMed   Mentions: 7     Fields:    Translation:Humans
      25. Cost-Effectiveness of Exome Sequencing versus Targeted Gene Panels for Prenatal Diagnosis of Fetal Effusions and Non-Immune Hydrops Fetalis. Am J Obstet Gynecol MFM. 2022 11; 4(6):100724. Avram CM, Caughey AB, Norton ME, Sparks TN. PMID: 35995366; PMCID: PMC9938838.
        View in: PubMed   Mentions: 1     Fields:    Translation:Humans
      26. Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology. Am J Med Genet C Semin Med Genet. 2022 06; 190(2):231-242. Dhombres F, Morgan P, Chaudhari BP, Filges I, Sparks TN, Lapunzina P, Roscioli T, Agarwal U, Aggarwal S, Beneteau C, Cacheiro P, Carmody LC, Collardeau-Frachon S, Dempsey EA, Dufke A, Duyzend MH, El Ghosh M, Giordano JL, Glad R, Grinfelde I, Iliescu DG, Ladewig MS, Munoz-Torres MC, Pollazzon M, Radio FC, Rodo C, Silva RG, Smedley D, Sundaramurthi JC, Toro S, Valenzuela I, Vasilevsky NA, Wapner RJ, Zemet R, Haendel MA, Robinson PN. PMID: 35872606; PMCID: PMC9588534.
        View in: PubMed   Mentions: 10     Fields:    Translation:Humans
      27. The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing. Prenat Diagn. 2022 09; 42(10):1288-1294. Swanson K, Norton ME, Lianoglou BR, Jelin AC, Hodoglugil U, Van Ziffle J, Devine P, Sparks TN. PMID: 35723972; PMCID: PMC9531346.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      28. "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 Genet. 2022; 13:882703. Brown JEH, Zamora AN, Outram S, Sparks TN, Lianoglou BR, Norstad M, Sahin Hodoglugil NN, Norton ME, Ackerman SL. PMID: 35669190; PMCID: PMC9164104.
        View in: PubMed   Mentions: 1  
      29. Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach. Genet Med. 2022 06; 24(6):1206-1216. Rego S, Hoban H, Outram S, Zamora AN, Chen F, Sahin-Hodoglugil N, Anguiano B, Norstad M, Yip T, Lianoglou B, Sparks TN, Norton ME, Koenig BA, Slavotinek AM, Ackerman SL. PMID: 35396980; PMCID: PMC9536515.
        View in: PubMed   Mentions: 5     Fields:    Translation:Humans
      30. Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis. Prenat Diagn. 2022 05; 42(5):611-616. Swanson K, Loeliger KB, Chetty SP, Sparks TN, Norton ME. PMID: 35106791; PMCID: PMC9116240.
        View in: PubMed   Mentions: 1     Fields:    Translation:Humans
      31. Prenatal presentation of multiple anomalies associated with haploinsufficiency for ARID1A. Eur J Med Genet. 2022 Feb; 65(2):104407. Slavotinek A, Lefebvre M, Brehin AC, Thauvin C, Patrier S, Sparks TN, Norton M, Yu J, Huang E. PMID: 34942405; PMCID: PMC9162882.
        View in: PubMed   Mentions: 5     Fields:    Translation:Humans
      32. Prenatal phenotype of 47, XXY (Klinefelter syndrome). Prenat Diagn. 2023 02; 43(2):207-212. Swanson K, Bishop JC, Al-Kouatly HB, Makhamreh M, Felton T, Vora NL, Sparks TN, Jelin AC. PMID: 34874073; PMCID: PMC9170827.
        View in: PubMed   Mentions: 3     Fields:    Translation:Humans
      33. The Current State and Future of Fetal Therapies. Clin Obstet Gynecol. 2021 12 01; 64(4):926-932. Sparks TN. PMID: 34560766; PMCID: PMC8530888.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      34. Response to "Further genetic testing in prenatal cases of nonimmune hydrops fetalis with a normal array: a targeted panel or exome?" Am J Obstet Gynecol. 2022 02; 226(2):277. Norton ME, Sparks TN. PMID: 34606761; PMCID: PMC8810662.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      35. Correction 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 Med. 2021 Oct; 23(10):2015. Gregg AR, Aarabi M, Klugman S, Leach NT, Bashford MT, Goldwaser T, Chen E, Sparks TN, Reddi HV, Rajkovic A, Dungan JS, ACMG Professional Practice and Guidelines Committee. PMID: 34453133; PMCID: PMC8776567.
        View in: PubMed   Mentions: 3     Fields:    
      36. Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis. Ultrasound Obstet Gynecol. 2021 Oct; 58(4):509-518. Mone F, Eberhardt RY, Hurles ME, Mcmullan DJ, Maher ER, Lord J, Chitty LS, Dempsey E, Homfray T, Giordano JL, Wapner RJ, Sun L, Sparks TN, Norton ME, Kilby MD. PMID: 33847422; PMCID: PMC8487902.
        View in: PubMed   Mentions: 14     Fields:    Translation:Humans
      37. Hypospadias. Am J Obstet Gynecol. 2021 11; 225(5):B18-B20. Society for Maternal-Fetal Medicine (SMFM), Sparks TN. PMID: 34507799.
        View in: PubMed   Mentions: 8     Fields:    Translation:Humans
      38. SMFM Fetal Anomalies Consult Series #4: Genitourinary anomalies. Am J Obstet Gynecol. 2021 11; 225(5):B2-B35. Society for Maternal-Fetal Medicine (SMFM). Electronic address: [email protected], Norton ME, Cheng Y, Chetty S, Chyu JK, Connolly K, Ghaffari N, Hopkins LM, Jelin A, Mardy A, Osmundson SS, Sparks TN, Sperling J, Swanson K, Zuckerwise LC, Kuller JA. PMID: 34507800; PMCID: PMC8763622.
        View in: PubMed   Mentions: 3     Fields:    Translation:Humans
      39. Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis. Am J Obstet Gynecol. 2022 01; 226(1):128.e1-128.e11. Norton ME, Ziffle JV, Lianoglou BR, Hodoglugil U, Devine WP, Sparks TN. PMID: 34331894; PMCID: PMC8748274.
        View in: PubMed   Mentions: 11     Fields:    Translation:Humans
      40. 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 Med. 2021 10; 23(10):1793-1806. Gregg AR, Aarabi M, Klugman S, Leach NT, Bashford MT, Goldwaser T, Chen E, Sparks TN, Reddi HV, Rajkovic A, Dungan JS, ACMG Professional Practice and Guidelines Committee. PMID: 34285390; PMCID: PMC8488021.
        View in: PubMed   Mentions: 76     Fields:    Translation:Humans
      41. Twin chorionicity and zygosity both vary with maternal age. Prenat Diagn. 2021 08; 41(9):1074-1079. Yeaton-Massey A, Sparks TN, Norton ME, Jelliffe-Pawlowski L, Currier RJ. PMID: 35280337; PMCID: PMC8916645.
        View in: PubMed   Mentions: 1     Fields:    Translation:Humans
      42. Preference for secondary findings in prenatal and pediatric exome sequencing. Prenat Diagn. 2022 05; 42(6):753-761. Swanson K, Sparks TN, Lianoglou BR, Chen F, Downum S, Patel S, Rego S, Yip T, Van Ziffle J, Koenig BA, Slavotinek AM, Norton ME. PMID: 34057224; PMCID: PMC8630094.
        View in: PubMed   Mentions: 7     Fields:    Translation:Humans
      43. Interval growth across gestation in pregnancies with fetal gastroschisis. Am J Obstet Gynecol MFM. 2021 09; 3(5):100415. Zhang-Rutledge K, Jacobs M, Patberg E, Field N, Holliman K, Strobel KM, Murphy A, Robles D, Rangwala N, Gonzalez JM, Sparks TN, University of California Fetal-Maternal Consortium. PMID: 34082169; PMCID: PMC8434973.
        View in: PubMed   Mentions: 2     Fields:    Translation:Humans
      44. Outcomes of Monochorionic, Diamniotic Twin Pregnancies with Prenatally Diagnosed Intertwin Weight Discordance. Am J Perinatol. 2021 06; 38(7):649-656. Sobhani NC, Sparks TN, Gosnell KA, Rand L, Gonzalez JM, Feldstein VA. PMID: 33321536; PMCID: PMC8164970.
        View in: PubMed   Mentions: 2     Fields:    Translation:Humans
      45. Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis. N Engl J Med. 2020 10 29; 383(18):1746-1756. Sparks TN, Lianoglou BR, Adami RR, Pluym ID, Holliman K, Duffy J, Downum SL, Patel S, Faubel A, Boe NM, Field NT, Murphy A, Laurent LC, Jolley J, Uy C, Slavotinek AM, Devine P, Hodoglugil U, Van Ziffle J, Sanders SJ, MacKenzie TC, Norton ME, University of California Fetal–Maternal Consortium, University of California, San Francisco Center for Maternal–Fetal Precision Medicine. PMID: 33027564; PMCID: PMC7650529.
        View in: PubMed   Mentions: 57     Fields:    Translation:Humans
      46. Variants of uncertain significance in prenatal microarrays: a retrospective cohort study. BJOG. 2021 01; 128(2):431-438. Mardy AH, Wiita AP, Wayman BV, Drexler K, Sparks TN, Norton ME. PMID: 32702189; PMCID: PMC7856034.
        View in: PubMed   Mentions: 9     Fields:    Translation:Humans
      47. The utility of exome sequencing for fetal pleural effusions. Prenat Diagn. 2020 04; 40(5):590-595. Jelin AC, Sobreira N, Wohler E, Solomon B, Sparks T, Sagaser KG, Forster KR, Miller J, Witmer PD, Hamosh A, Valle D, Blakemore K. PMID: 31994743; PMCID: PMC7383284.
        View in: PubMed   Mentions: 3     Fields:    Translation:Humans
      48. Utility of chromosomal microarray for diagnosis in cases of nonimmune hydrops fetalis. Prenat Diagn. 2020 03; 40(4):492-496. Mardy AH, Rangwala N, Hernandez-Cruz Y, Gosnell KA, Gonzalez JM, Norton ME, Sparks TN. PMID: 31981373; PMCID: PMC7153803.
        View in: PubMed   Mentions: 9     Fields:    Translation:Humans
      49. Anthropogenic control over wintertime oxidation of atmospheric pollutants. Geophys Res Lett. 2019 Dec 28; 46(24):14826-14835. Haskins JD, Lopez-Hilfiker FD, Lee BH, Shah V, Wolfe GM, DiGangi J, Fibiger D, McDuffie EE, Veres P, Schroder JC, Campuzano-Jost P, Day DA, Jimenez JL, Weinheimer A, Sparks T, Cohen RC, Campos T, Sullivan A, Guo H, Weber R, Dibb J, Greene J, Fiddler M, Bililign S, Jaeglé L, Brown SS, Thornton JA. PMID: 33012881; PMCID: PMC7526063.
        View in: PubMed   Mentions: 5  
      50. The utility of nuchal translucency ultrasound in identifying rare chromosomal abnormalities not detectable by cell-free DNA screening. Prenat Diagn. 2020 01; 40(2):185-190. Berger VK, Norton ME, Sparks TN, Flessel M, Baer RJ, Currier RJ. PMID: 31652356; PMCID: PMC7002253.
        View in: PubMed   Mentions: 3     Fields:    Translation:Humans
      51. Expanded carrier screening: counseling and considerations. Hum Genet. 2020 Sep; 139(9):1131-1139. Sparks TN. PMID: 31679051; PMCID: PMC7195224.
        View in: PubMed   Mentions: 12     Fields:    Translation:Humans
      52. Cell-free fetal DNA screening for detection of microdeletion syndromes: a cost-effectiveness analysis. J Matern Fetal Neonatal Med. 2021 Jun; 34(11):1732-1740. Avram CM, Shaffer BL, Sparks TN, Allen AJ, Caughey AB. PMID: 31327283; PMCID: PMC7000293.
        View in: PubMed   Mentions: 3     Fields:    Translation:Humans
      53. A system-based approach to the genetic etiologies of non-immune hydrops fetalis. Prenat Diagn. 2019 08; 39(9):732-750. Mardy AH, Chetty SP, Norton ME, Sparks TN. PMID: 31087399; PMCID: PMC6699893.
        View in: PubMed   Mentions: 12     Fields:    Translation:Humans
      54. Nonimmune hydrops fetalis: identifying the underlying genetic etiology. Genet Med. 2019 06; 21(6):1339-1344. Sparks TN, Thao K, Lianoglou BR, Boe NM, Bruce KG, Datkhaeva I, Field NT, Fratto VM, Jolley J, Laurent LC, Mardy AH, Murphy AM, Ngan E, Rangwala N, Rottkamp CAM, Wilson L, Wu E, Uy CC, Valdez Lopez P, Norton ME, University of California Fetal–Maternal Consortium (UCfC). PMID: 30410095; PMCID: PMC6509016.
        View in: PubMed   Mentions: 25     Fields:    Translation:Humans
      55. Fetal Congenital Pulmonary Airway Malformation: The Role of an Objective Measurement of Cardiomediastinal Shift. Am J Perinatol. 2019 02; 36(3):225-232. Shulman R, Sparks TN, Gosnell K, Blat C, Norton ME, Lee H, Gonzalez-Velez J, Goldstein RB. PMID: 30199894; PMCID: PMC6372337.
        View in: PubMed   Mentions: 4     Fields:    Translation:Humans
      56. How should costs and cost-effectiveness be considered in prenatal genetic testing? Semin Perinatol. 2018 08; 42(5):275-282. Sparks TN, Caughey AB. PMID: 30173949; PMCID: PMC6204084.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      57. Stage I Twin-Twin Transfusion Syndrome: Outcomes of Expectant Management and Prognostic Features. Am J Perinatol. 2018 12; 35(14):1352-1357. Washburn EE, Sparks TN, Gosnell KA, Rand L, Gonzalez JM, Feldstein VA. PMID: 29528469; PMCID: PMC6082735.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      58. Prenatal Diagnosis of Congenital Diaphragmatic Hernia: Does Laterality Predict Perinatal Outcomes? Am J Perinatol. 2018 08; 35(10):919-924. Sperling JD, Sparks TN, Berger VK, Farrell JA, Gosnell K, Keller RL, Norton ME, Gonzalez JM. PMID: 29304545; PMCID: PMC6033692.
        View in: PubMed   Mentions: 8     Fields:    Translation:Humans
      59. Utility of chromosomal microarray in anomalous fetuses. Prenat Diagn. 2018 01; 38(2):140-147. Parchem JG, Sparks TN, Gosnell K, Norton ME. PMID: 29297200; PMCID: PMC5828907.
        View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
      60. Polyhydramnios Affecting a Recipient-like Twin: Risk of Progression to Twin-Twin Transfusion Syndrome and Outcomes. Am J Perinatol. 2018 03; 35(4):317-323. Washburn EE, Sparks TN, Gosnell KA, Rand L, Gonzalez JM, Feldstein VA. PMID: 29287298; PMCID: PMC5842126.
        View in: PubMed   Mentions: 1     Fields:    Translation:Humans
      61. Non-Immune Hydrops Fetalis: Do Placentomegaly and Polyhydramnios Matter? J Ultrasound Med. 2018 May; 37(5):1185-1191. Berger VK, Sparks TN, Jelin AC, Derderian C, Jeanty C, Gosnell K, Mackenzie T, Gonzalez JM. PMID: 29076544; PMCID: PMC6029704.
        View in: PubMed   Mentions: 4     Fields:    Translation:Humans
      62. The growth-restricted fetus: risk of mortality by each additional week of expectant management. J Matern Fetal Neonatal Med. 2019 Feb; 32(3):442-447. Pilliod RA, Page JM, Sparks TN, Caughey AB. PMID: 28974133; PMCID: PMC6033681.
        View in: PubMed   Mentions: 4     Fields:    Translation:Humans
      63. Potential Role of Genomic Sequencing in the Early Diagnosis of Treatable Genetic Conditions. J Pediatr. 2017 10; 189:222-226.e1. Zahed H, Sparks TN, Li B, Alsadah A, Shieh JTC. PMID: 28947054; PMCID: PMC6037534.
        View in: PubMed   Mentions: 3     Fields:    Translation:Humans
      64. Mosaic trisomy 16: what are the obstetric and long-term childhood outcomes? Genet Med. 2017 10; 19(10):1164-1170. Sparks TN, Thao K, Norton ME. PMID: 28383546; PMCID: PMC6029708.
        View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
      65. Observed Rate of Down Syndrome in Twin Pregnancies. Obstet Gynecol. 2016 11; 128(5):1127-1133. Sparks TN, Norton ME, Flessel M, Goldman S, Currier RJ. PMID: 27741202.
        View in: PubMed   Mentions: 7     Fields:    Translation:Humans
      66. Gastroschisis: mortality risks with each additional week of expectant management. Am J Obstet Gynecol. 2017 Jan; 216(1):66.e1-66.e7. Sparks TN, Shaffer BL, Page J, Caughey AB. PMID: 27596619.
        View in: PubMed   Mentions: 8     Fields:    Translation:Humans
      67. Maternal arrhythmia and perinatal outcomes. J Perinatol. 2016 10; 36(10):823-7. Henry D, Gonzalez JM, Harris IS, Sparks TN, Killion M, Thiet MP, Bianco K. PMID: 27309629; PMCID: PMC5045765.
        View in: PubMed   Mentions: 8     Fields:    Translation:Humans
      68. Hypertension in dichorionic twin gestations: how is birthweight affected? J Matern Fetal Neonatal Med. 2017 Feb; 30(4):380-385. Sparks TN, Nakagawa S, Gonzalez JM. PMID: 27046743.
        View in: PubMed   Mentions: 9     Fields:    Translation:Humans
      69. Down syndrome: perinatal mortality risks with each additional week of expectant management. Prenat Diagn. 2016 Apr; 36(4):368-74. Sparks TN, Griffin E, Page J, Pilliod R, Shaffer BL, Caughey AB. PMID: 26891366.
        View in: PubMed   Mentions: 5     Fields:    Translation:Humans
      70. How do maternal views of delivery outcomes vary by demographics and preferred mode of delivery? Am J Perinatol. 2015 Jul; 32(8):741-6. Sparks TN, Yeaton-Massey A, Granados JM, Handler SJ, Meyer M, Caughey AB. PMID: 25519201.
        View in: PubMed   Mentions: 2     Fields:    Translation:Humans
      71. Preference toward future mode of delivery: how do antepartum preferences and prior delivery experience contribute? J Matern Fetal Neonatal Med. 2015; 28(14):1673-8. Sparks TN, Yeaton-Massey A, Granados JM, Handler SJ, Meyer MR, Caughey AB. PMID: 25212977.
        View in: PubMed   Mentions:    Fields:    Translation:Humans
      72. Predictors of cesarean delivery in women undergoing labor induction with a Foley balloon. J Matern Fetal Neonatal Med. 2015 Jun; 28(9):1000-4. Delaney S, Shaffer BL, Cheng YW, Vargas J, Sparks TN, Paul K, Caughey AB. PMID: 25012806.
        View in: PubMed   Mentions: 3     Fields:    Translation:Humans
      73. Racial/ethnic variations in perineal length and association with perineal lacerations: a prospective cohort study. J Matern Fetal Neonatal Med. 2015 Feb; 28(3):320-3. Yeaton-Massey A, Wong L, Sparks TN, Handler SJ, Meyer MR, Granados JM, Stasenko M, Sit A, Caughey AB. PMID: 24749802.
        View in: PubMed   Mentions: 7     Fields:    Translation:Humans
      74. The cost-effectiveness of repeat HIV testing during pregnancy in a resource-limited setting. J Acquir Immune Defic Syndr. 2013 Jun 01; 63(2):195-200. Kim LH, Cohan DL, Sparks TN, Pilliod RA, Arinaitwe E, Caughey AB. PMID: 23392461; PMCID: PMC3653987.
        View in: PubMed   Mentions: 11     Fields:    Translation:HumansCellsPHPublic Health
      75. Does risk of preeclampsia differ by twin chorionicity? J Matern Fetal Neonatal Med. 2013 Sep; 26(13):1273-7. Sparks TN, Cheng YW, Phan N, Caughey AB. PMID: 23425367.
        View in: PubMed   Mentions: 12     Fields:    Translation:Humans
      76. Impending macrosomia: will induction of labour modify the risk of caesarean delivery? BJOG. 2012 Mar; 119(4):402-9. Cheng YW, Sparks TN, Laros RK, Nicholson JM, Caughey AB. PMID: 22251443; PMCID: PMC3428793.
        View in: PubMed   Mentions: 6     Fields:    Translation:Humans
      77. Treating mild gestational diabetes mellitus: a cost-effectiveness analysis. Am J Obstet Gynecol. 2011 Sep; 205(3):282.e1-7. Ohno MS, Sparks TN, Cheng YW, Caughey AB. PMID: 22071065; PMCID: PMC3443977.
        View in: PubMed   Mentions: 31     Fields:    Translation:Humans
      78. Patient counseling increases postpartum follow-up in women with gestational diabetes mellitus. Am J Obstet Gynecol. 2011 Jun; 204(6):522.e1-6. Stasenko M, Liddell J, Cheng YW, Sparks TN, Killion M, Caughey AB. PMID: 21514559; PMCID: PMC3425434.
        View in: PubMed   Mentions: 31     Fields:    Translation:Humans
      79. The effect of cesarean delivery rates on the future incidence of placenta previa, placenta accreta, and maternal mortality. J Matern Fetal Neonatal Med. 2011 Nov; 24(11):1341-6. Solheim KN, Esakoff TF, Little SE, Cheng YW, Sparks TN, Caughey AB. PMID: 21381881.
        View in: PubMed   Mentions: 54     Fields:    Translation:Humans
      80. Diagnosis and morbidity of placenta accreta. Ultrasound Obstet Gynecol. 2011 Mar; 37(3):324-7. Esakoff TF, Sparks TN, Kaimal AJ, Kim LH, Feldstein VA, Goldstein RB, Cheng YW, Caughey AB. PMID: 20812377.
        View in: PubMed   Mentions: 11     Fields:    Translation:Humans
      81. Fundal height: a useful screening tool for fetal growth? J Matern Fetal Neonatal Med. 2011 May; 24(5):708-12. Sparks TN, Cheng YW, McLaughlin B, Esakoff TF, Caughey AB. PMID: 20849205.
        View in: PubMed   Mentions: 25     Fields:    Translation:HumansPHPublic Health
      82. Labor induction with a Foley balloon inflated to 30 mL compared with 60 mL: a randomized controlled trial. Obstet Gynecol. 2010 Jun; 115(6):1239-1245. Delaney S, Shaffer BL, Cheng YW, Vargas J, Sparks TN, Paul K, Caughey AB. PMID: 20502296.
        View in: PubMed   Mentions: 23     Fields:    Translation:Humans
      83. The association between birthweight 4000 g or greater and perinatal outcomes in patients with and without gestational diabetes mellitus. Am J Obstet Gynecol. 2009 Jun; 200(6):672.e1-4. Esakoff TF, Cheng YW, Sparks TN, Caughey AB. PMID: 19376489.
        View in: PubMed   Mentions: 61     Fields:    Translation:Humans
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