Faculty

Institution

Unit

Venue

Stephen Braddock

Saint Louis University

Affiliations

School of Medicine

Department of Pediatrics

Pediatric Medical Genetics

NoneStephen Braddock is currently serving as a Pediatrics faculty at Saint Louis University.

Honors

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Experiences

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Education

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Stephen Braddock

Saint Louis University

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genetics human genetics medical genetics genomics molecular genetics developmental biology genome biology hematology pediatrics neurology genetic disorders respiratory medicine epigenetics neurogenetics intellectual disability cardiovascular research vascular biology developmental genetics cytogenetics gene expression population genetics mammalian biology molecular physiology pediatric allergy mutagenesis applied genetics host genetics genome instability retrospective cohort studies prospective cohort studies neonatology case studies valvular heart disease epigenomics birth outcomes novo variants cohen syndrome liver physiology clinical biochemistry molecular metabolism arthritis brain tumor research avian biology scientific data adrenal glands adrenal disease pediatric endocrinology endocrine research developmental endocrinology cataracts cancer genetics cancer genomics animal genetics mitochondrial function myocardial infarction genetic factors genomic mechanisms cancer screening developmental epidemiology valve disease fetal medicine pediatric hematology health care supervision tissue distribution variable expression lysosomal storage disorders genotype-phenotype analysis congenital adrenal hyperplasia oxidoreductase deficiency down syndrome-like facies cerebellar malformations etiologic landscape phenotypic analysis essential component urogenital anomalies

Notable Scholarly Works

Notable Federal Grants

Collaborators

Clinical Characterization of Collagen XII ‐Related Disease Caused by Biallelic Col12A1 Variants. Annals of Clinical and Translational Neurology (2025)

Riley M. McCartyDimah SaadePinki MunotChamindra G. LavertyHailey PinzYaqun ZouMeghan McAnallyPomi YunCuixia TianYing HuLucy FengRahul PhadkeSophia CeulemansPilar MagoulasAndrew J. SkalskyJennifer R. FriedmanStephen R. BraddockSarah B. NeuhausDenise M. MalickiMatthew N. BainbridgeShareef NahasDavid P. DimmockStephen F. KingsmoreTimothy E. LotzeA. Reghan FoleyFrancesco MuntoniVolker StraubSandra DonkervoortCarsten G. Bönnemann

neurologyurologyclinical neuroscienceclinical characterizationclinical neurologyneurodegenerative diseases

Co-Existence of Coloboma, Heart Defects, Atresia Choanae, Growth Retardation, Genital Abnormalities, and Ear Anomalies (Charge) Syndrome and Heterotaxy in a Newborn With Athymia. Journal of Allergy and Clinical Immunology Global (2025)

Rica PatilJacquelyn HunterAlan KnutsenStephen R. Braddock

immunologygrowth retardationclinical immunologyatresia choanaeasthmaallergyheart defectsgenital abnormalitiespediatric allergyear anomalies

Cover Image, Volume 193, Number 2, June 2023. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023)

Benjamin SolomonAnne SlavotinekJohn CareyJohn OpitzManaging EditorGrainne CaffreyEdward ClarkUta FranckeJudith HallRaoul HennekamArno MotulskyGiovanni NeriNorio NiikawaJoe SimpsonJürgen SprangerMargaret AdamYasemin AlanayHolly ArdingerMichael BamshadDiana BianchiStephen BraddockDavid ChitayatCynthia CurryWilliam DobynsJill FahrnerJohn GrahamK DorothyFiorella GrangeRudolf GurrieriTerry HappleNik HassoldHülya KantaputraTomoki KayseriliIan KoshoRalph KrantzPablo LachmanAngela LapunzinaRick LinNaomichi MartinJulie MatsumotoStefan McgaughranJeffrey MundlosShubha MurrayWillie PhadkeRobert ReardonStephen RestaNathaniel RobertsonRavi RobinAlbert SavarirayanGary SchinzelRichard ShawAndrea SmithKaren Superti-FurgaAlain TempleIshwar VerloesDavid VermaRosanna Viskochil

medical imagingmedical geneticsgeneticscover image

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria. JAMA Neurology (2023)

Shyam K. AkulaAllen Y. ChenJennifer E. NeilDiane D. ShaoAlisa MoNorma K. HyltonStephanie DiTroiaVijay S. GaneshRichard S. SmithKatherine O’KaneRebecca C. YehJack H. MarcianoSamantha KirkhamConnor J. KennyJanet H. T. SongMuna Al SaffarFrancisca MillanDavid J. HarrisAndrea V. MurphyKara C. KlempStephen R. BraddockHarrison BrandIsaac WongMichael E. TalkowskiAnne O’Donnell-LuriaAbbe LaiRobert Sean HillGaneshwaran H. MochidaRyan N. DoanA. James BarkovichEdward YangDina AmromEva AndermannAnnapurna PoduriChristopher A. WalshBassam Abu-LibdehLihadh Al-GazaliMuna Al SaffarEdith Alva MoncayoDina AmromEva AndermanAnna-Kaisa AnttonenSaunder BarnesSara BarnettTodd BarronBrenda J. BarryLina Basel-VanagaiteLaila BastakiLuis Bello-EspinosaTawfeg Ben-OmranMatthew BernardCarsten G. BonnemanBlaise BourgeoisStephen BrownRoberto H. CaraballoGergory CascinoMichael ClarkeMonika CohenYanick CrowBernard DanKira A. DiesWilliam B. DobynsFrançois DubeauChristelle El AchkarGregory M. EnnsLaurence FaivreLaura Flores-SarnatJohn GaitanisKuchukhidze GiorgiAndrew GreenAlan GubermanRenzo GuerriniMicheil InnesRichard JacobsenSebastian JacquemontSamir KhalilJoerg KlepperDimitri KranicKalpathy KrishnamoorthyAnna-Elina LehesjokiDorit LevRichard J. LeventerEmily LisiValerie Loik RameySally Ann LynchLaila MahmoudDavid ManchesterDavid MandelbaumDaphna MaromDeborah MarsdenMayra Martinez OjedaAmira MasriLivija MedneDenis MelansonDavid T. MillerAnna MinsterEdward NeilanDang Khoa NguyenHeather E. OlsonIgnacio Pascual-Castroviejo

genomicsneurologygenome biologyepigenomicsgenomic mechanismsgeneticsexome sequencingmolecular geneticsepigeneticshuman geneticsneuroscienceneuroanatomy

Omenn Syndrome in a 10-Month-Old Male With Athymia and Vacterl Association. Journal of Allergy and Clinical Immunology Global (2023)

Bimaljit K. PangliStephen R. BraddockAlan P. Knutsen

immunologyomenn syndromeclinical immunologyhematologyclinical allergyallergyglobal health

Table of Contents, Volume 193, Number 1, March 2023. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023)

genomicsmedical geneticsgenetics

Table of Contents, Volume 193, Number 2, June 2023. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023)

medical geneticsgeneticshematology

Biallelic Alterations in Plxnd1 Cause Common Arterial Trunk and Other Cardiac Malformations in Humans. Human Molecular Genetics (2022)

Anne GuimierLoïc de PontualStephen R BraddockErin TortiLuis A Pérez-JuradoPatricia Muñoz-CabelloMontserrat ArumíKristin G MonaghanHane LeeLee-kai WangIlina D PluymSally Ann LynchKaren StalsSian EllardCécile MullerLucile HouyelLaurence CohenStanislas LyonnetFanny BajolleJeanne AmielChristopher T Gordon

cardiologygenomicsgenome biologystructural heart diseasecardiovascular researchvascular biologyvascular malformationsgeneticsvalvular heart diseasebiallelic alterationsmolecular biologymolecular geneticsrespiratory medicinedevelopmental biologymedical geneticshuman geneticshuman biologyarterial disease

Table of Contents, Volume 190, Number 4, December 2022. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022)

Benjamin SolomonAnne Slavo�John CareyJohn OpitzElle CumberbatchEdward ClarkUta FranckeJudith HallRaoul HennekamArno MotulskyGiovanni NeriNorio NiikawaCharles ScriverJoe SimpsonJürgen SprangerMargaret AdamYasemin AlanayHolly ArdingerMichael BamshadDiana BianchiStephen BraddockDavid ChitayatCynthia CurryWilliam DobynsJill FahrnerJohn GrahamK DorothyFiorella GrangeRudolf GurrieriTerry HappleNik HassoldHülya KantaputraTomoki KayseriliIan KoshoRalph KrantzPablo LachmanAngela LapunzinaRick LinNaomichi MatsumotoJulie McgaughranStefan MundlosJeff ReyC MurrayShubha PhadkeWillie ReardonRobert RestaStephen RobertsonNathaniel RobinRavi SavarirayanAlbert SchinzelGary ShawRichard SmithAndrea Super� -FurgaKaren TempleAlain VerloesIshwar VermaDavid ViskochilRosanna WeksbergChiara LeoniMartin ZenkerMarco TartagliaYoko AokiBruce GelbAngelica DeloguGiuseppe LimongelliPaolo VersacciRachele AdorisioJuan KaskiRita BlandinoStella MaioloEmanuele MondaCarolina PutottoGabriella De RosaKathryn ChatfieldGiulio CalcagniMaria KavamuraDavid StevensonGermana ViscogliosiFederica TamburrinoEmanuela ScaranoConcetta SchiavarielloAnnamaria PerriAndrea PessionLaura MazzantiRoberta OnesimoValentina GiorgioElisabetta SforzaEliza KuczynskaGaia MargiottaMariella IademarcoFrancesco ProliDonato RiganteGiuseppe ZampinoK WeaverKaren GrippDaniel Kenney-JungDante RogersSamuel KroeningAbigail ZatkalikAshley Whitmarsh

genomicsmedical geneticsgeneticshealth sciences

Birth Outcomes in Women Who Have Taken Hydroxycholoroquine During Pregnancy: A Prospective Cohort Study. Arthritis & Rheumatology (2021)

Christina D. ChambersDiana L. JohnsonRonghui XuYunjun LuoRobert FelixMinh FineChloe LessardMargaret P. AdamStephen R. BraddockLuther K. RobinsonLeah BurkeKenneth Lyons Jones

arthritisrheumatologyprospective cohort studiesretrospective cohort studiesbirth outcomeshealth scienceswomen's health

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Stephen Braddock

Saint Louis University

Affiliations

School of Medicine

Department of Pediatrics

Pediatric Medical Genetics

NoneStephen Braddock is currently serving as a Pediatrics faculty at Saint Louis University.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Stephen Braddock

Saint Louis University

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Clinical Characterization of Collagen XII ‐Related Disease Caused by Biallelic Col12A1 Variants. Annals of Clinical and Translational Neurology (2025)

neurologyurologyclinical neuroscienceclinical characterizationclinical neurologyneurodegenerative diseases

Rica PatilJacquelyn HunterAlan KnutsenStephen R. Braddock

immunologygrowth retardationclinical immunologyatresia choanaeasthmaallergyheart defectsgenital abnormalitiespediatric allergyear anomalies

Cover Image, Volume 193, Number 2, June 2023. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023)

medical imagingmedical geneticsgeneticscover image

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria. JAMA Neurology (2023)

genomicsneurologygenome biologyepigenomicsgenomic mechanismsgeneticsexome sequencingmolecular geneticsepigeneticshuman geneticsneuroscienceneuroanatomy

Omenn Syndrome in a 10-Month-Old Male With Athymia and Vacterl Association. Journal of Allergy and Clinical Immunology Global (2023)

Bimaljit K. PangliStephen R. BraddockAlan P. Knutsen

immunologyomenn syndromeclinical immunologyhematologyclinical allergyallergyglobal health

Table of Contents, Volume 193, Number 1, March 2023. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023)

genomicsmedical geneticsgenetics

Table of Contents, Volume 193, Number 2, June 2023. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023)

medical geneticsgeneticshematology

Biallelic Alterations in Plxnd1 Cause Common Arterial Trunk and Other Cardiac Malformations in Humans. Human Molecular Genetics (2022)

Table of Contents, Volume 190, Number 4, December 2022. American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022)

genomicsmedical geneticsgeneticshealth sciences

Birth Outcomes in Women Who Have Taken Hydroxycholoroquine During Pregnancy: A Prospective Cohort Study. Arthritis & Rheumatology (2021)

Christina D. ChambersDiana L. JohnsonRonghui XuYunjun LuoRobert FelixMinh FineChloe LessardMargaret P. AdamStephen R. BraddockLuther K. RobinsonLeah BurkeKenneth Lyons Jones

arthritisrheumatologyprospective cohort studiesretrospective cohort studiesbirth outcomeshealth scienceswomen's health

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3
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5
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