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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

The Challenge of Risk Stratification of Infants Born Preterm in the Setting of Competing and Disparate Healthcare Outcomes.
Whitehead HV, McPherson CC, Vesoulis ZA, Cohlan BA, Rao R, Warner BB, Cole FS
J Pediatr. 2020 Aug; 223194-196. doi: 10.1016/j.jpeds.2020.04.043.

PMID:
    32711746
    [PubMed - in process]
Related citations


Functional Genomics of ATP-Binding Cassette Transporter A3 (<i>ABCA3</i>) Variants.
Wambach JA, Yang P, Wegner DJ, Heins HB, Luke C, Li F, White FV, Cole FS
Am J Respir Cell Mol Biol. 2020 Jul 21; doi: 10.1165/rcmb.2020-0034MA.

PMID:
    32692933
    [PubMed - as supplied by publisher]
Related citations


Precise breakpoint detection in a patient with 9p- syndrome.
Ng J, Sams E, Baldridge D, Kremitzki M, Wegner DJ, Lindsay T, Fulton R, Cole FS, Turner TN
Cold Spring Harb Mol Case Stud. 2020 Jun; 6(3)pii: a005348. doi: 10.1101/mcs.a005348.

PMID:
    32532883
    [PubMed - in process]
Related citations


De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.
Mao D, Reuter CM, Ruzhnikov MRZ, Beck AE, Farrow EG, Emrick LT, Rosenfeld JA, Mackenzie KM, Robak L, Wheeler MT, Burrage LC, Jain M, Liu P, Calame D, Küry S, Sillesen M, Schmitz-Abe K, Tonduti D, Spaccini L, Iascone M, Genetti CA, Koenig MK, Graf M, Tran A, Alejandro M, Undiagnosed Diseases Network., Lee BH, Thiffault I, Agrawal PB, Bernstein JA, Bellen HJ, Chao HT
Am J Hum Genet. 2020 Apr 2; 106(4)570-583. doi: 10.1016/j.ajhg.2020.02.016.

PMID:
    32197074
    [PubMed - indexed for MEDLINE]
Related citations


Phenotypic expansion of KMT2D-related disorder: Beyond Kabuki syndrome.
Baldridge D, Spillmann RC, Wegner DJ, Wambach JA, White FV, Sisco K, Toler TL, Dickson PI, Cole FS, Shashi V, Grange DK
Am J Med Genet A. 2020 May; 182(5)1053-1065. doi: 10.1002/ajmg.a.61518.

PMID:
    32083401
    [PubMed - in process]
Related citations


Acute Kidney Injury and Bronchopulmonary Dysplasia in Premature Neonates Born Less than 32 Weeks' Gestation.
Starr MC, Boohaker L, Eldredge LC, Menon S, Griffin R, Mayock DE, Li L, Askenazi D, Hingorani S, Neonatal Kidney Collaborative.
Am J Perinatol. 2020 Feb; 37(3)341-348. doi: 10.1055/s-0039-3400311.

PMID:
    31777046
    [PubMed - in process]
Related citations


Acute Kidney Injury is Associated with Poor Lung Outcomes in Infants Born ≥32 Weeks of Gestational Age.
Starr MC, Boohaker L, Eldredge LC, Menon S, Griffin R, Mayock D, Askenazi D, Hingorani S, Neonatal Kidney Collaborative.
Am J Perinatol. 2020 Jan; 37(2)231-240. doi: 10.1055/s-0039-1698836.

PMID:
    31739364
    [PubMed - indexed for MEDLINE]
Related citations


Incidence and Risk Factors of Early Onset Neonatal AKI.
Charlton JR, Boohaker L, Askenazi D, Brophy PD, D'Angio C, Fuloria M, Gien J, Griffin R, Hingorani S, Ingraham S, Mian A, Ohls RK, Rastogi S, Rhee CJ, Revenis M, Sarkar S, Smith A, Starr M, Kent AL, Neonatal Kidney Collaborative.
Clin J Am Soc Nephrol. 2019 Feb 7; 14(2)184-195. doi: 10.2215/CJN.03670318.

PMID:
    31738181
    [PubMed - indexed for MEDLINE]
Related citations


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 - indexed for MEDLINE]
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. 2020 Mar/Apr; 35(2)177-185. doi: 10.1177/1062860619850322.

PMID:
    31115254
    [PubMed - in process]
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 - indexed for MEDLINE]
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 - indexed for MEDLINE]
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 - indexed for MEDLINE]
Related citations


Addressing medically underserved populations through maternal-fetal transport: a geographic analysis.
Rosenbloom JI, Nelson DM, Saunders S, Cole FS, Chandarlis J, Macones GA, Cahill AG
J Matern Fetal Neonatal Med. 2020 Sep; 33(17)2913-2917. doi: 10.1080/14767058.2018.1564028.

PMID:
    30585099
    [PubMed - in process]
Related citations


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 - indexed for MEDLINE]
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 - indexed for MEDLINE]
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 - indexed for MEDLINE]
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

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