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F. Sessions Cole, MD

Park J. White, M.D., Professor of Pediatrics
Professor of Cell Biology and Physiology
Assistant Vice Chancellor for Children’s Health
Vice Chairman, Department of Pediatrics
Director, Division of Newborn Medicine
Chief Medical Officer, St. Louis Children’s Hospital

Specialty Areas

Newborn Medicine - Neonatology
Neonatal/Perinatal Medicine

Board Certifications

Neonatal-Perinatal Medicine
Pediatrics

Hospital Affiliations

Barnes-Jewish Hospital
St. Louis Children's Hospital

Areas of Clinical Interest

Inherited lung diseases of infancy, surfactant protein-B deficiency, newborn immunity, newborn infections, complement biosynthesis

  • Location(s)
  • Education
  • Publication & Research
  • In the News

Location(s)

Location(s)

St. Louis Children’s Hospital

1 Children’s Place
St. Louis, MO 63110

Suite: Neonatal Intensive Care Unit (NICU), 5th Floor
Office Phone: 314-454-6148
Fax: 314-454-4633

Education

Education

Fellowship: Research in Neonatology and Cell Biology, the Joint Program in Neonatology, Brigham and Women's Hosp 1981
Residency: Senior Assistant, The Children's Hospital Medical Center, Boston, Massachusetts 1978
Residency: Junior Assistant, The Children's Hospital Medical Center, Boston, Massachusetts 1977
Medical Officer: General Medical Officer, United States Public Health Service Hospital, Brighton, Massachusetts 1976
Internship: Pediatrics, The Children's Hospital Medical Center, Boston, Massachusetts 1974
MD: Yale University School of Medicine, New Haven, Connecticut 1973
B.A.: Amherst College, Amherst, Massachusetts 1969

Publication & Research

Publication & Research

De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.
Kanca O, Andrews JC, Lee PT, Patel C, Braddock SR, Slavotinek AM, Cohen JS, Gubbels CS, Aldinger KA, Williams J, Indaram M, Fatemi A, Yu TW, Agrawal PB, Vezina G, Simons C, Crawford J, Lau CC, Undiagnosed Diseases Network., Chung WK, Markello TC, Dobyns WB, Adams DR, Gahl WA, Wangler MF, Yamamoto S, Bellen HJ, Malicdan MCV
Am J Hum Genet. 2019 Aug 1; 105(2)413-424. doi: 10.1016/j.ajhg.2019.06.014.

PMID:
    31327508
    [PubMed - in process]
Related citations


Use of EHR-Based Pediatric Quality Measures: Views of Health System Leaders and Parents.
Hartley DM, Jonas S, Grossoehme D, Kelly A, Dodds C, Alford SM, Shenkman E, Simmons J, Bailey LC, Razzaghi H, Utidjian LH, McCafferty-Fernandez J, Cole FS, Smallwood J, Werk LN, Walsh KE
Am J Med Qual. 2019 May 22; 1062860619850322. doi: 10.1177/1062860619850322.

PMID:
    31115254
    [PubMed - as supplied by publisher]
Related citations


Phenotype and response to growth hormone therapy in siblings with B4GALT7 deficiency.
Sandler-Wilson C, Wambach JA, Marshall BA, Wegner DJ, McAlister W, Cole FS, Shinawi M
Bone. 2019 Jul; 12414-21. doi: 10.1016/j.bone.2019.03.029.

PMID:
    30914273
    [PubMed - in process]
Related citations


CemOrange2 fusions facilitate multifluorophore subcellular imaging in C. elegans.
Thomas BJ, Wight IE, Chou WYY, Moreno M, Dawson Z, Homayouni A, Huang H, Kim H, Jia H, Buland JR, Wambach JA, Cole FS, Pak SC, Silverman GA, Luke CJ
PLoS One. 2019; 14(3)e0214257. doi: 10.1371/journal.pone.0214257.

PMID:
    30913273
    [PubMed - in process]
Related citations


Optimizing the AKI definition during first postnatal week using Assessment of Worldwide Acute Kidney Injury Epidemiology in Neonates (AWAKEN) cohort.
Askenazi D, Abitbol C, Boohaker L, Griffin R, Raina R, Dower J, Davis TK, Ray PE, Perazzo S, DeFreitas M, Milner L, Ambalavanan N, Cole FS, Rademacher E, Zappitelli M, Mhanna M, Neonatal Kidney Collaborative.
Pediatr Res. 2019 Feb; 85(3)329-338. doi: 10.1038/s41390-018-0249-8.

PMID:
    30643188
    [PubMed - in process]
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Late onset neonatal acute kidney injury: results from the AWAKEN Study.
Charlton JR, Boohaker L, Askenazi D, Brophy PD, Fuloria M, Gien J, Griffin R, Hingorani S, Ingraham S, Mian A, Ohls RK, Rastogi S, Rhee CJ, Revenis M, Sarkar S, Starr M, Kent AL, Neonatal Kidney Collaborative (NKC).
Pediatr Res. 2019 Feb; 85(3)339-348. doi: 10.1038/s41390-018-0255-x.

PMID:
    30546043
    [PubMed - in process]
Related citations


Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome.
Wambach JA, Wegner DJ, Patni N, Kircher M, Willing MC, Baldridge D, Xing C, Agarwal AK, Vergano SAS, Patel C, Grange DK, Kenney A, Najaf T, Nickerson DA, Bamshad MJ, Cole FS, Garg A
Am J Hum Genet. 2018 Dec 6; 103(6)968-975. doi: 10.1016/j.ajhg.2018.10.010.

PMID:
    30414627
    [PubMed - indexed for MEDLINE]
Related citations


Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizures.
Wambach JA, Wegner DJ, Yang P, Shinawi M, Baldridge D, Betleja E, Shimony JS, Spencer D, Hackett BP, Andrews MV, Ferkol T, Dutcher SK, Mahjoub MR, Cole FS
Pediatr Res. 2018 Sep; 84(3)435-441. doi: 10.1038/s41390-018-0083-z.

PMID:
    29967526
    [PubMed - in process]
Related citations


Functional Assays to Screen and Dissect Genomic Hits: Doubling Down on the National Investment in Genomic Research.
Musunuru K, Bernstein D, Cole FS, Khokha MK, Lee FS, Lin S, McDonald TV, Moskowitz IP, Quertermous T, Sankaran VG, Schwartz DA, Silverman EK, Zhou X, Hasan AAK, Luo XJ
Circ Genom Precis Med. 2018 Apr; 11(4)e002178. doi: 10.1161/CIRCGEN.118.002178.

PMID:
    29654098
    [PubMed - indexed for MEDLINE]
Related citations


Mutations in the thyroid transcription factor gene NKX2-1 result in decreased expression of SFTPB and SFTPC.
Attarian SJ, Leibel SL, Yang P, Alfano DN, Hackett BP, Cole FS, Hamvas A
Pediatr Res. 2018 Sep; 84(3)419-425. doi: 10.1038/pr.2018.30.

PMID:
    29538355
    [PubMed - in process]
Related citations


Gene variants of the phosphatidylcholine synthesis pathway do not contribute to RDS in the Chinese population.
Chen YJ, Meyer J, Wambach JA, DePass K, Wegner DJ, Fan X, Zhang QY, Hillary H, Cole FS, Hamvas A
World J Pediatr. 2018 Feb; 14(1)52-56. doi: 10.1007/s12519-017-0109-3.

PMID:
    29411327
    [PubMed - indexed for MEDLINE]
Related citations


Infants with Atypical Presentations of Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins Who Underwent Bilateral Lung Transplantation.
Towe CT, White FV, Grady RM, Sweet SC, Eghtesady P, Wegner DJ, Sen P, Szafranski P, Stankiewicz P, Hamvas A, Cole FS, Wambach JA
J Pediatr. 2018 Mar; 194158-164.e1. doi: 10.1016/j.jpeds.2017.10.026.

PMID:
    29198536
    [PubMed - indexed for MEDLINE]
Related citations


Neonatal Outcomes Differ after Spontaneous and Indicated Preterm Birth.
Stout MJ, Demaree D, Merfeld E, Tuuli MG, Wambach JA, Cole FS, Cahill AG
Am J Perinatol. 2018 Apr; 35(5)494-502. doi: 10.1055/s-0037-1608804.

PMID:
    29183099
    [PubMed - indexed for MEDLINE]
Related citations


Differentiation of Human Pluripotent Stem Cells into Functional Lung Alveolar Epithelial Cells.
Jacob A, Morley M, Hawkins F, McCauley KB, Jean JC, Heins H, Na CL, Weaver TE, Vedaie M, Hurley K, Hinds A, Russo SJ, Kook S, Zacharias W, Ochs M, Traber K, Quinton LJ, Crane A, Davis BR, White FV, Wambach J, Whitsett JA, Cole FS, Morrisey EE, Guttentag SH, Beers MF, Kotton DN
Cell Stem Cell. 2017 Oct 5; 21(4)472-488.e10. doi: 10.1016/j.stem.2017.08.014.

PMID:
    28965766
    [PubMed - indexed for MEDLINE]
Related citations


The Genomics of Neonatal Abstinence Syndrome.
Cole FS, Wegner DJ, Davis JM
Front Pediatr. 2017; 5176. doi: 10.3389/fped.2017.00176.

PMID:
    28879171
    [PubMed]
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Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN).
Wambach JA, Stettner GM, Haack TB, Writzl K, Škofljanec A, Maver A, Munell F, Ossowski S, Bosio M, Wegner DJ, Shinawi M, Baldridge D, Alhaddad B, Strom TM, Grange DK, Wilichowski E, Troxell R, Collins J, Warner BB, Schmidt RE, Pestronk A, Cole FS, Steinfeld R
Hum Mutat. 2017 Nov; 38(11)1477-1484. doi: 10.1002/humu.23297.

PMID:
    28726266
    [PubMed - indexed for MEDLINE]
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Families as Partners in Hospital Error and Adverse Event Surveillance.
Khan A, Coffey M, Litterer KP, Baird JD, Furtak SL, Garcia BM, Ashland MA, Calaman S, Kuzma NC, O'Toole JK, Patel A, Rosenbluth G, Destino LA, Everhart JL, Good BP, Hepps JH, Dalal AK, Lipsitz SR, Yoon CS, Zigmont KR, Srivastava R, Starmer AJ, Sectish TC, Spector ND, West DC, Landrigan CP, the Patient and Family Centered I-PASS Study Group., Allair BK, Alminde C, Alvarado-Little W, Atsatt M, Aylor ME, Bale JF Jr, Balmer D, Barton KT, Beck C, Bismilla Z, Blankenburg RL, Chandler D, Choudhary A, Christensen E, Coghlan-McDonald S, Cole FS, Corless E, Cray S, Da Silva R, Dahale D, Dreyer B, Growdon AS, Gubler L, Guiot A, Harris R, Haskell H, Kocolas I, Kruvand E, Lane MM, Langrish K, Ledford CJW, Lewis K, Lopreiato JO, Maloney CG, Mangan A, Markle P, Mendoza F, Micalizzi DA, Mittal V, Obermeyer M, O'Donnell KA, Ottolini M, Patel SJ, Pickler R, Rogers JE, Sanders LM, Sauder K, Shah SS, Sharma M, Simpkin A, Subramony A, Thompson ED Jr, Trueman L, Trujillo T, Turmelle MP, Warnick C, Welch C, White AJ, Wien MF, Winn AS, Wintch S, Wolf M, Yin HS, Yu CE
JAMA Pediatr. 2017 Apr 1; 171(4)372-381. doi: 10.1001/jamapediatrics.2016.4812.

PMID:
    28241211
    [PubMed - indexed for MEDLINE]
Related citations


Outcomes of Lung Transplantation for Infants and Children with Genetic Disorders of Surfactant Metabolism.
Eldridge WB, Zhang Q, Faro A, Sweet SC, Eghtesady P, Hamvas A, Cole FS, Wambach JA
J Pediatr. 2017 May; 184157-164.e2. doi: 10.1016/j.jpeds.2017.01.017.

PMID:
    28215425
    [PubMed - indexed for MEDLINE]
Related citations


Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome.
Wambach JA, Yang P, Wegner DJ, Heins HB, Kaliberova LN, Kaliberov SA, Curiel DT, White FV, Hamvas A, Hackett BP, Cole FS
Am J Respir Cell Mol Biol. 2016 Nov; 55(5)716-721.

PMID:
    27374344
    [PubMed - indexed for MEDLINE]
Related citations


Genetic Factors Contribute to Risk for Neonatal Respiratory Distress Syndrome among Moderately Preterm, Late Preterm, and Term Infants.
Shen CL, Zhang Q, Meyer Hudson J, Cole FS, Wambach JA
J Pediatr. 2016 May; 17269-74.e2. doi: 10.1016/j.jpeds.2016.01.031.

PMID:
    26935785
    [PubMed - indexed for MEDLINE]
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In the News