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Author Details

Ning Shang
Columbia University Irving Medical Center
2008
60
16
PMIDPaper TitleJournal TitlePublished Year
36302597Genomic Disorders in CKD across the Lifespan.J Am Soc Nephrol2023
38036523Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.Nat Commun2023
35862291Spontaneously ruptured multilocular cystic nephroma in an infant.J Clin Ultrasound2023
37214819Polygenic risk affects the penetrance of monogenic kidney disease.medRxiv2023
36969276American college of radiology ovarian-adnexal reporting and data system ultrasound (O-RADS): Diagnostic performance and inter-reviewer agreement for ovarian masses in children.Front Pediatr2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
36521849Prenatal ultrasound evaluation of fetal cutaneous hemangioma and related complications.J Matern Fetal Neonatal Med2023
36474423Characterizing variability of electronic health record-driven phenotype definitions.J Am Med Inform Assoc2023
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
36737471Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.Sci Rep2023
36670513Fetal agenesis of the septum pellucidum: Ultrasonic diagnosis and clinical significance.Prenat Diagn2023
34101608Joint Landmark and Structure Learning for Automatic Evaluation of Developmental Dysplasia of the Hip.IEEE J Biomed Health Inform2022
35710995Genome-wide polygenic score to predict chronic kidney disease across ancestries.Nat Med2022
35673021Evaluation of Criteria2Query: Towards Augmented Intelligence for Cohort Identification.Stud Health Technol Inform2022
35394661Prenatal ultrasonic features of a mediastinal teratoma: A case report and literature review.J Clin Ultrasound2022
36468023Case report and a brief review: Analysis and challenges of prenatal imaging phenotypes and genotypes in Joubert syndrome.Front Genet2022
35928450Paternal De Novo Variant of <i>TAOK1</i> in a Fetus With Structural Brain Abnormalities.Front Genet2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
35090449Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.BMC Med Inform Decis Mak2022
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
31039657Application of the LMS method of constructing fetal reference charts: comparison with the original method.J Matern Fetal Neonatal Med2021
33850243Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.NPJ Digit Med2021
33610881Similarity-based health risk prediction using Domain Fusion and electronic health records data.J Biomed Inform2021
34869125Congenital Visceral Vascular Variation Causing Gastrointestinal Hemorrhage: A Case Report.Front Pediatr2021
34642645Elevated Neutrophil Gelatinase-Associated Lipocalin Is Associated With the Severity of Kidney Injury and Poor Prognosis of Patients With COVID-19.Kidney Int Rep2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
34686147The liver steatosis severity and lipid characteristics in primary biliary cholangitis.BMC Gastroenterol2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
33941608Medical Records-Based Genetic Studies of the Complement System.J Am Soc Nephrol2021
34302027Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies.NPJ Digit Med2021
34347061Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry.JAMA Netw Open2021
34142015Comparative effectiveness of medical concept embedding for feature engineering in phenotyping.JAMIA Open2021
34282949Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.Circ Genom Precis Med2021
32929784Prenatal sonographic diagnosis of partial left pulmonary artery sling: A rare case report.J Clin Ultrasound2021
32952152Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.Int J Obes (Lond)2021
32719840A graph-based method for reconstructing entities from coordination ellipsis in medical text.J Am Med Inform Assoc2020
31866433Adapting electronic health records-derived phenotypes to claims data: Lessons learned in using limited clinical data for phenotyping.J Biomed Inform2020
33398295Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.medRxiv2020
33134165Evaluating the Treatment Efficacy of Nano-Drug in a Lung Cancer Model Using Advanced Functional Magnetic Resonance Imaging.Front Oncol2020
30753493Criteria2Query: a natural language interface to clinical databases for cohort definition.J Am Med Inform Assoc2019
31655273Ensembles of natural language processing systems for portable phenotyping solutions.J Biomed Inform2019
31405830Development and Validation of a Pragmatic Electronic Phenotype for CKD.Clin J Am Soc Nephrol2019
30988330Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.Sci Rep2019
30892098Penetration of different molecule sizes upon ultrasound combined with microbubbles in a superficial tumour model.J Drug Target2019
28670732Prenatal sonographic diagnosis of nondysraphic intramedullary lipomas: A case report.J Clin Ultrasound2018
30124903A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments.J Am Med Inform Assoc2018
30815192Low Screening Rates for Diabetes Mellitus Among Family Members of Affected Relatives.AMIA Annu Symp Proc2018
30395248Effect of vocabulary mapping for conditions on phenotype cohorts.J Am Med Inform Assoc2018
29703846LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.Circulation2018
29025047The representativeness of eligible patients in type 2 diabetes trials: a case study using GIST 2.0.J Am Med Inform Assoc2018
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Collaborators

Chunhua Weng
Columbia University Irving Medical Center
Co-authored papers 22
George Hripcsak
Columbia University
Co-authored papers 16
Krzysztof Kiryluk
Columbia University
Co-authored papers 15
Ali G Gharavi
Columbia University College of Physicians and Surgeons
Co-authored papers 11
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 10
Joshua C Denny
Vanderbilt University
Co-authored papers 10
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 9
David R Crosslin
University of Washington Medical Center
Co-authored papers 9
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 8
Eric B Larson
University of Washington
Co-authored papers 7
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers 7
Elizabeth W Karlson
Brigham and Women's Hospital
Co-authored papers 6
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 6
Peggy L Peissig
Center for Precision Medicine Research, Marshfield Clinic Research Institute
Co-authored papers 6
David S Carrell
Kaiser Permanente Washington Health Research Institute
Co-authored papers 6
Patrick B Ryan
Columbia University Irving Medical Center
Co-authored papers 6
Luke V Rasmussen
Northwestern University Feinberg School of Medicine
Co-authored papers 5
Bahram Namjou
Cincinnati Children's Hospital
Co-authored papers 5
Adam S Gordon
Northwestern University Feinberg School of Medicine.
Co-authored papers 5
Ian B Stanaway
Kidney Research Institute and Division of Nephrology, University of Washington
Co-authored papers 5
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 5
Robert J Carroll
Vanderbilt University Medical Center
Co-authored papers 4
Marc S Williams
University of Washington Medical Center
Co-authored papers 4
Scott J Hebbring
Marshfield Clinic Research Institute
Co-authored papers 4
Vivian S Gainer
Co-authored papers 4
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 4
Casey N Ta
Columbia University Irving Medical Center
Co-authored papers 4
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 4
Kenneth M Borthwick
Hood Center for Health Research
Co-authored papers 3
Mathieu Bourgey
McGill University
Co-authored papers 3
Release 1.2