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Author Details

Sarah U Morton
Boston Children's Hospital
2006
61
19
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
38001156Establishing a neonatology consultation program: extending care beyond the neonatal intensive care unit.J Perinatol2024
38009418Association of genetic and sulcal traits with executive function in congenital heart disease.Ann Clin Transl Neurol2024
36183910The Genetics of Neurodevelopment in Congenital Heart Disease.Can J Cardiol2023
37392599Association of cerebral metabolic rate following therapeutic hypothermia with 18-month neurodevelopmental outcomes after neonatal hypoxic ischemic encephalopathy.EBioMedicine2023
37348522Paenibacillus spp infection among infants with postinfectious hydrocephalus in Uganda: an observational case-control study.Lancet Microbe2023
37179381Preterm congenital heart disease and neurodevelopment: the importance of looking beyond the initial hospitalization.J Perinatol2023
37305724Challenges in the clinical understanding of genetic testing in birth defects and pediatric diseases.Transl Pediatr2023
37165897Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease.Circ Genom Precis Med2023
36722669Tethered cord syndrome in KBG syndrome.Am J Med Genet A2023
36803080Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.Circ Genom Precis Med2023
36701153Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease.JAMA Netw Open2023
34272501Genomic frontiers in congenital heart disease.Nat Rev Cardiol2022
35707545Premature Infants Have Normal Maturation of the T Cell Receptor Repertoire at Term.Front Immunol2022
35584116An ancient founder mutation located between <i>ROBO1</i> and <i>ROBO2</i> is responsible for increased microtia risk in Amerindigenous populations.Proc Natl Acad Sci U S A2022
35698050mirTarRnaSeq: An R/Bioconductor Statistical Package for miRNA-mRNA Target Identification and Interaction Analysis.BMC Genomics2022
35397206Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk.Am J Hum Genet2022
35815018A Role for Data Science in Precision Nutrition and Early Brain Development.Front Psychiatry2022
35684014Increased Breastfeeding Proportion Is Associated with Improved Gross Motor Skills at 3-5 Years of Age: A Pilot Study.Nutrients2022
36374038Type IV Pili Are a Critical Virulence Factor in Clinical Isolates of Paenibacillus thiaminolyticus.mBio2022
35909108Fetal Disseminated Malignant Rhabdoid Tumor.Neoreviews2022
35254387Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review.JAMA Neurol2022
35130025Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity.Circ Genom Precis Med2022
35182466Transcription factor protein interactomes reveal genetic determinants in heart disease.Cell2022
35150915Cytomegalovirus infections in infants in Uganda: Newborn-mother pairs, neonates with sepsis, and infants with hydrocephalus.Int J Infect Dis2022
34009260Abnormal Right-Hemispheric Sulcal Patterns Correlate with Executive Function in Adolescents with Tetralogy of Fallot.Cereb Cortex2021
33557580Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency.Circ Res2021
33799993microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy.Int J Mol Sci2021
33913194Quantification of magnetic resonance spectroscopy data using a combined reference: Application in typically developing infants.NMR Biomed2021
33912816Immune activation during <i>Paenibacillus</i> brain infection in African infants with frequent cytomegalovirus co-infection.iScience2021
35011057Assessment of Maternal Macular Pigment Optical Density (MPOD) as a Potential Marker for Dietary Carotenoid Intake during Lactation in Humans.Nutrients2021
34610948Reducing Benzodiazepine Exposure by Instituting a Guideline for Dexmedetomidine Usage in the NICU.Pediatrics2021
31216004Abnormal Left-Hemispheric Sulcal Patterns Correlate with Neurodevelopmental Outcomes in Subjects with Single Ventricular Congenital Heart Disease.Cereb Cortex2020
33054971<i>GATA6</i> mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm.Elife2020
33216750Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles.PLoS Genet2020
32771363Association of nucleated red blood cell count with mortality among neonatal intensive care unit patients.Pediatr Neonatol2020
32998967<i>Paenibacillus</i> infection with frequent viral coinfection contributes to postinfectious hydrocephalus in Ugandan infants.Sci Transl Med2020
32601476Genomic analyses implicate noncoding de novo variants in congenital heart disease.Nat Genet2020
32812804De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease.Circ Genom Precis Med2020
32426625Screening With Reticulocyte Hemoglobin Increased Iron Sufficiency Among NICU Patients.Pediatr Qual Saf2020
32396742Congenital Heart Defects Due to <i>TAF1</i> Missense Variants.Circ Genom Precis Med2020
30262924Response to Brodehl et al.Genet Med2019
31792156Psychosocial Stress and Adversity: Effects from the Perinatal Period to Adulthood.Neoreviews2019
29961767Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.Genet Med2019
31292440Paternal-age-related de novo mutations and risk for five disorders.Nat Commun2019
30707697Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.PLoS Genet2019
29740193Reducing time to initiation and advancement of enteral feeding in an all-referral neonatal intensive care unit.J Perinatol2018
30098192Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.Invest Ophthalmol Vis Sci2018
27858371Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants.JIMD Rep2017
28299359<i>AIFM1</i> mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant.Cold Spring Harb Mol Case Stud2017
28991257Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.Nat Genet2017
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Collaborators

Christine E Seidman
Brigham and Women's Hospital (Y.K.
Co-authored papers 19
Jonathan G Seidman
Harvard Medical School
Co-authored papers 17
Bruce D Gelb
Icahn School of Medicine at Mount Sinai
Co-authored papers 12
Elizabeth Goldmuntz
Co-authored papers 12
Jane W Newburger
Boston Children's Hospital
Co-authored papers 12
Deepak Srivastava
Gladstone Institutes San Francisco
Co-authored papers 10
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 10
Martina Brueckner
Co-authored papers 10
George A Porter
Co-authored papers 10
Pankaj B Agrawal
Broad Institute of MIT and Harvard
Co-authored papers 9
Patricia Ellen Grant
Boston Children's Hospital, Harvard Medical School
Co-authored papers 8
Steven R DePalma
Co-authored papers 8
Richard Kim
Co-authored papers 8
Martin Tristani-Firouzi
Co-authored papers 8
Amy E Roberts
Boston Children's Hospital, Harvard Medical School
Co-authored papers 7
Daniel Bernstein
Co-authored papers 7
Yufeng Shen
Columbia University
Co-authored papers 6
Alessandro Giardini
Co-authored papers 5
Richard P Lifton
The Rockefeller University
Co-authored papers 4
Alexandre C Pereira
Co-authored papers 4
Catherine A Brownstein
Harvard Medical School.
Co-authored papers 3
Alan H Beggs
Broad Institute of MIT and Harvard
Co-authored papers 3
Benoit G Bruneau
Gladstone Institutes of Cardiovascular Disease, Gladstone Institutes
Co-authored papers 3
Kathryn N Ivey
Gladstone Institutes, USA Roddenberry Center for Stem Cell Biology at Gladstone
Co-authored papers 3
David C Bellinger
Boston Children's Hospital
Co-authored papers 3
Eileen King
Cincinnati Children's Hospital Medical Center
Co-authored papers 2
Donald J Hagler
Center for Multimodal Imaging and Genetics, University of California San Diego
Co-authored papers 2
Michael J Rivkin
Boston Children's Hospital, Harvard Medical School
Co-authored papers 2
Mark J Cowley
Children's Cancer Institute, Lowy Cancer Research Centre
Co-authored papers 2
Diane Fatkin
Co-authored papers 2
Release 1.2