ID

45642

Description

Principal Investigator: Roberta L. Hannibal, Stanford University School of Medicine, Stanford, CA, USA MeSH: Pre-eclampsia,Hypertension, Pregnancy-Induced,Diabetes, Gestational,Premature Birth,Anemia,Trisomy,Abnormalities https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001320 Chorionic villus sampling (CVS) is routinely used for prenatal diagnosis of cytogenetic disorders, but also possesses great potential for studying placentation. To better understand villi biology, human placentation, and how these relate to pregnancy outcomes, we examined the morphology and transcriptomes of villi obtained via CVS from 10-14 weeks of pregnancy and correlated these with pregnancy attributes and clinical outcomes.

Link

dbGaP study = phs001320

Keywords

  1. 3/13/23 3/13/23 - Simon Heim
Copyright Holder

Roberta L. Hannibal, Stanford University School of Medicine, Stanford, CA, USA

Uploaded on

March 13, 2023

DOI

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License

Creative Commons BY 4.0

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dbGaP phs001320 Investigating Human Placentation and Pregnancy Using First Trimester Chorionic Villi

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Inclusion Criteria: Pregnant women undergoing CVS from March 2012 to March 2013 at Lucile Packard Children's Hospital.
Description

Inclusion Criteria: Pregnant women undergoing CVS from March 2012 to March 2013 at Lucile Packard Children's Hospital.

Data type

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0033011
UMLS CUI [1,3]
C2163625
UMLS CUI [1,4]
C0008509
UMLS CUI [1,5]
C1442880
UMLS CUI [1,6]
C0020017
Exclusion Criteria: Women who did not consent to this study; women with CV samples that were not scored for morphology, women with CV samples which did not have clinical information linked to the CV samples.
Description

Exclusion Criteria: Women who did not consent to this study; women with CV samples that were not scored for morphology, women with CV samples which did not have clinical information linked to the CV samples.

Data type

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0742765
UMLS CUI [1,3]
C0043210
UMLS CUI [1,4]
C0008509
UMLS CUI [1,5]
C4700202
UMLS CUI [1,6]
C0332437
UMLS CUI [1,7]
C2708733

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Inclusion Criteria: Pregnant women undergoing CVS from March 2012 to March 2013 at Lucile Packard Children's Hospital.
Item
Inclusion Criteria: Pregnant women undergoing CVS from March 2012 to March 2013 at Lucile Packard Children's Hospital.
boolean
C1512693 (UMLS CUI [1,1])
C0033011 (UMLS CUI [1,2])
C2163625 (UMLS CUI [1,3])
C0008509 (UMLS CUI [1,4])
C1442880 (UMLS CUI [1,5])
C0020017 (UMLS CUI [1,6])
Exclusion Criteria: Women who did not consent to this study; women with CV samples that were not scored for morphology, women with CV samples which did not have clinical information linked to the CV samples.
Item
Exclusion Criteria: Women who did not consent to this study; women with CV samples that were not scored for morphology, women with CV samples which did not have clinical information linked to the CV samples.
boolean
C0680251 (UMLS CUI [1,1])
C0742765 (UMLS CUI [1,2])
C0043210 (UMLS CUI [1,3])
C0008509 (UMLS CUI [1,4])
C4700202 (UMLS CUI [1,5])
C0332437 (UMLS CUI [1,6])
C2708733 (UMLS CUI [1,7])

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