Search Results - "Screening Tests"

Is intermediate risk really intermediate? Comparison of karyotype and non-invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening.

Alkan Bulbul G; Division of Perinatology, Department of Gynecology and Obstetrics, Akdeniz University Faculty of Medicine, Antalya, Turkey., Kirtis E; Division of Perinatology, Department of Gynecology and Obstetrics, Akdeniz University Faculty of Medicine, Antalya, Turkey., Kandemir H; Division of Perinatology, Department of Gynecology and Obstetrics, Akdeniz University Faculty of Medicine, Antalya, Turkey., Sanhal CY; Division of Perinatology, Department of Gynecology and Obstetrics, Akdeniz University Faculty of Medicine, Antalya, Turkey., Yakut Uzuner S; Department of Medical Biology and Genetics, Akdeniz University Faculty of Medicine, Antalya, Turkey., Karauzum SB; Department of Medical Biology and Genetics, Akdeniz University Faculty of Medicine, Antalya, Turkey., Mendilcioglu II; Division of Perinatology, Department of Gynecology and Obstetrics, Akdeniz University Faculty of Medicine, Antalya, Turkey.

Journal Article; Comparative Study , 2025

Exploring the Potential of Generative AI to Support Non-Experts in Learning Analytics Practice

Xavier Ochoa (ORCID 0000-0002-4371-7701), Xiaomeng Huang (ORCID 0000-0002-6992-061X), Yuli Shao (ORCID 0009-0002-3726-0677)

Y

Wish and Care Method: Empowering Women for Breast Cancer Screening

Wigi Anis Nursanti (ORCID 0009-0009-3030-7920), Nanik Setiyawati (ORCID 0000-0002-7131-7510), Heni Puji Wahyuningsih (ORCID 0000-0003-2238-6402)

Y

High positive predictive value 22q11.2 microdeletion screening by prenatal cell-free DNA testing that incorporates fetal fraction amplification.

Hammer C; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Pierson S; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Acevedo A; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Goldberg J; Independent (unaffiliated), Washington, District of Columbia, USA., Westover T; Maternal Fetal Medicine and Perinatal Genetics, Capital Health, Trenton, New Jersey, USA., Chawla D; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Mabey B; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Muzzey D; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Johansen Taber K; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA.

Journal Article; Research Support, Non-U.S. Gov't , 2024

Numbers of prenatal cell-free DNA screens performed: Results of a 2022 CAP exercise.

Palomaki GE; Department of Pathology and Laboratory Medicine, Alpert Medical School at Brown University, Women & Infants Hospital of RI, Providence, Rhode Island, USA., Wyatt P; Esoterix Genetic Laboratories, Santa Fe, New Mexico, USA., Rowsey R; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA., Cacheris PM; Sequenom Laboratories, San Diego, California, USA., Lepage N; Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Natowicz MR; Pathology and Laboratory Medicine, Genomic Medicine, Neurology and Pediatrics Institutes, Cleveland Clinic, Cleveland, Ohio, USA., Long T; Department of Biostatistics, College of American Pathologists, Northfield, Illinois, USA., Moyer AM; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Journal Article , 2024

The Guilford ROCS (Readiness of Children for School) Study. Overview

Shira Mattera, Carolyn J. Hill, MDRC

N

Duke Endowment

Programming for the Language Disabled Child: Booklet 1: Identification Procedures.

Texas Education Agency, Austin.

N

Project CHILD: Final Report.

Texas Education Agency, Austin.

N

Implementing New or Expanded Early Head Start Services after Converting Slots: Findings from the HS2EHS Case Studies. OPRE Report #2024-310

Diane Schilder, Catherine Kuhns, Kate Stepleton, Carly Morrison, Administration for Children and Families (DHHS), Office of Planning, Research and Evaluation (OPRE), Urban Institute, MEF Associates

N

Think Again: Are Education Programs for High-Achievers Inherently Inequitable?

Brandon L. Wright, Thomas B. Fordham Institute

N

Thomas B. Fordham Foundation

Circulating Cell-free DNA and Screening for Trisomies.

Norton ME; From the Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, San Francisco.

Journal Article , 2022

Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study.

Zhang M; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Gao Y; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Liang M; Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China., Wang Y; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China., Guo L; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Wu D; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Xiao H; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Lin L; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Wang H; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China. wanghongdan@zzu.edu.cn.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China. wanghongdan@zzu.edu.cn., Liao S; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China. ychsgy@126.com.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China. ychsgy@126.com.

Journal Article; Research Support, Non-U.S. Gov't , 2024

Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines.

Dreux S; Biochimie-Hormonologie, Hôpital R. Debré, DMU Biogem AP-HP, Paris, France.; Fédération des CPDPN, Paris, France., Rosenblatt J; Fédération des CPDPN, Paris, France.; Gynécologie-Obstétrique, Hôpital Robert Debré, AP-HP, Paris, France., Massardier J; Fédération des CPDPN, Paris, France.; Gynécologie-Obstétrique, HFME, Hospices Civils de Lyon, Lyon, France.; Centre Français de Référence des Maladies Trophoblastiques, Pierre Bénite, France., Benachi A; Fédération des CPDPN, Paris, France.; Gynécologie-Obstétrique, Hôpital Antoine Béclère, AP-HP, Université Paris Saclay Clamart, Paris, France., Voirin-Mathieu E; Biochimie-Hormonologie, Hôpital R. Debré, DMU Biogem AP-HP, Paris, France., Muller F; Biochimie-Hormonologie, Hôpital R. Debré, DMU Biogem AP-HP, Paris, France.; Fédération des CPDPN, Paris, France.

ABA Study Group

Journal Article; Multicenter Study , 2024

Primary cell-free DNA screening or contingent screening for the common trisomies: a response.

Dar P; Department of Obstetrics and Gynecology and Women's Health, Montefiore Medical Center, Albert Einstein College of Medicine, 1695 Eastchester Rd., Ste. L4, Bronx, NY 10461. Electronic address: peerdar@gmail.com., Norton ME; Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, San Francisco, CA.

Letter; Research Support, Non-U.S. Gov't; Comment , 2022

Performance of cell-free DNA testing for common fetal trisomies in triplet pregnancies.

Zakaria H; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France., Kleinfinger P; Laboratoire Cerba, Saint-Ouen l'Aumône, France., Lohmann L; Laboratoire Cerba, Saint-Ouen l'Aumône, France., Costa JM; Laboratoire Cerba, Saint-Ouen l'Aumône, France., Tsatsaris V; Division of Obstetrics and Gynecology, 'Port Royal' Hospital, Paris Cité University, APHP, Paris, France., Salomon LJ; Division of Obstetrics and Gynecology, 'Necker-Enfants Malades' Hospital, Paris Cité University, APHP, Paris, France., Jouannic JM; Division of Fetal Medicine, 'Armand Trousseau' Hospital, Sorbonne Paris Nord University, APHP, Paris, France., Rosenblatt J; Division of Obstetrics and Gynecology, 'Robert Debré' Hospital, Sorbonne Paris Nord University, APHP, Paris, France., Demain A; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France., Benachi A; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France., El Khattabi L; Non-Invasive Prenatal Screening laboratory, APHP, Paris Cité University, Hôpital Cochin, Paris, France.; Chromosomal Genomics Unit, Medical Genetics Department, APHP, Sorbonne Paris Nord University, Armand Trousseau and Pitié-Salpêtrière Hospitals, Paris, France., Vivanti AJ; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France.

Journal Article , 2024

Laboratory Testing of Hemostasis in Pregnancy: A Brief Overview

Othman, Maha^{Aff4, Aff5, Aff6}, Pradhan, Anushka^Aff4

Favaloro, Emmanuel J.^Aff2, Gosselin, Robert C.^Aff3, Walker, John M.^Aff1

Classes of Student Emotion as Predictive of Academic Achievement

Caroline Mierzwa (ORCID 0000-0001-5256-3102), Nathaniel von der Embse, Eunsook Kim, Melissa Brown

Y

The Factor Structure of the Strengths and Difficulties Questionnaire (SDQ) in India

Hina Sheel (ORCID 0000-0001-8814-2123), Lidia Suárez, Nigel V. Marsh (ORCID 0000-0002-4060-6432)

Y

The Conflation of Dual Language Bilingual Education with Gifted Programs in New York City Schools

Allison Roda (ORCID 0000-0002-3685-7052), Kate Menken (ORCID 0000-0003-2330-5547)

Y

Identifying Children at Risk for Emotional and Behavioral Problems: A Diagnostic Classification Model Approach

Yu Bao, Jin Liu (ORCID 0000-0001-5816-2422), Christine DiStefano, Ruyi Ding

Y