Billie Lianoglou
Genetic Program Crd
Surgery
School of Medicine

Publications (23)

Top publication keywords:
Enzyme Replacement TherapyFetal DiseasesUrethral ObstructionWT1 ProteinsLysosomal Storage DiseasesExomeCOUP Transcription Factor IIalpha-ThalassemiaMuscular Atrophy, SpinalPrenatal DiagnosisUltrasonography, PrenatalHydrops FetalisGlycogen Storage Disease Type IIFetusFetal Therapies

• Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies.
  Prenatal diagnosis 2023 Rothschild HT, Lianoglou BR, Sahin Hodoglugil NN, Tick K, Brown JEH, Sparks TN
• Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects.
  Prenatal diagnosis 2023 Herzeg A, Borges B, Lianoglou BR, Gonzalez-Velez J, Canepa E, Munar D, Young SP, Bali D, Gelb MH, Chakraborty P, Kishnani PS, Harmatz P, Cohen JL, MacKenzie TC
• Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
  NPJ genomic medicine 2023 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…
• Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.
  Prenatal diagnosis 2023 Sahin-Hodoglugil NN, Lianoglou BR, Ackerman S, Sparks TN, Norton ME
• The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction.
  Prenatal diagnosis 2023 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 …

Show all (18 more) Hide

• Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
  NPJ genomic medicine 2023 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…
• The impact of in utero transfusions on perinatal outcomes in patients with alpha thalassemia major: the UCSF registry.
  Blood advances 2023 Schwab ME, Lianoglou BR, Gano D, Gonzalez Velez J, Allen IE, Arvon R, Baschat A, Bianchi DW, Bitanga M, Bourguignon A, Brown RN, Chen B, Chien M, Davis-Nelson S, de Laat MWM, Ekwattanakit S, Gollin Y,…
• Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.
  Prenatal diagnosis 2022 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, …
• In Utero Enzyme-Replacement Therapy for Infantile-Onset Pompe's Disease.
  The New England journal of medicine 2022 Cohen JL, Chakraborty P, Fung-Kee-Fung K, Schwab ME, Bali D, Young SP, Gelb MH, Khaledi H, DiBattista A, Smallshaw S, Moretti F, Wong D, Lacroix C, El Demellawy D, Strickland KC, Lougheed J, Moon-…
• Investigating attitudes toward prenatal diagnosis and fetal therapy for spinal muscular atrophy.
  Prenatal diagnosis 2022 Schwab ME, Shao S, Zhang L, Lianoglou B, Belter L, Jarecki J, Schroth M, Sumner CJ, MacKenzie T
• Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI-FDA Meeting).
  Journal of clinical pharmacology 2022 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
• The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing.
  Prenatal diagnosis 2022 Swanson K, Norton ME, Lianoglou BR, Jelin AC, Hodoglugil U, Van Ziffle J, Devine P, Sparks TN
• "Let's Just Wait Until She's Born": Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic Research.
  Frontiers in genetics 2022 Brown JEH, Zamora AN, Outram S, Sparks TN, Lianoglou BR, Norstad M, Sahin Hodoglugil NN, Norton ME, Ackerman SL
• Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach.
  Genetics in medicine : official journal of the American College of Medical Genetics 2022 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
• Fetal therapies and trials for lysosomal storage diseases: a survey of attitudes of parents and patients.
  Orphanet journal of rare diseases 2022 Schwab ME, Brown JEH, Lianoglou B, Jin C, Conroy PC, Gallagher RC, Harmatz P, MacKenzie TC
• Consensus statement for the perinatal management of patients with α thalassemia major.
  Blood advances 2021 MacKenzie TC, Amid A, Angastiniotis M, Butler C, Gilbert S, Gonzalez J, Keller RL, Kharbanda S, Kirby-Allen M, Koenig BA, Kyono W, Lal A, Lianoglou BR, Norton ME, Ogasawara KK, Panchalee T, Rosner M, …
• Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis.
  American journal of obstetrics and gynecology 2021 Norton ME, Ziffle JV, Lianoglou BR, Hodoglugil U, Devine WP, Sparks TN
• Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants.
  American journal of surgery 2021 Schwab ME, Dong S, Lianoglou BR, Aguilar Lucero AF, Schwartz GB, Norton ME, MacKenzie TC, Sanders SJ
• Preference for secondary findings in prenatal and pediatric exome sequencing.
  Prenatal diagnosis 2021 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
• Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium.
  Journal of personalized medicine 2021 Suckiel SA, O'Daniel JM, Donohue KE, Gallagher KM, Gilmore MJ, Hendon LG, Joseph G, Lianoglou BR, Mathews JM, Norton ME, Odgis JA, Poss AF, Rego S, Scollon S, Yip T, Amendola LM
• Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
  The New England journal of medicine 2020 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 …
• Nonimmune hydrops fetalis: identifying the underlying genetic etiology.
  Genetics in medicine : official journal of the American College of Medical Genetics 2018 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,…
• Favorable outcomes after in utero transfusion in fetuses with alpha thalassemia major: a case series and review of the literature.
  Prenatal diagnosis 2016 Kreger EM, Singer ST, Witt RG, Sweeters N, Lianoglou B, Lal A, Mackenzie TC, Vichinsky E