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Jerold W. Wallis, MD

Associate Professor, Radiology
Division of Nuclear Medicine

Specialty Areas

Radiology
Nuclear Medicine

Board Certifications

Internal Medicine
Nuclear Medicine

Hospital Affiliations

Barnes-Jewish Hospital
Barnes-Jewish West County Hospital
St. Louis Children's Hospital

Areas of Clinical Interest

Nuclear medicine, nuclear imaging, PET, positron emission tomography, radioiodine treatment, radionuclide imaging, teleradiology, PACS (Picture Archival and Communication Systems)

  • Maps & Directions
  • Education
  • Publication & Research

Maps & Directions

Maps & Directions

Barnes-Jewish Hospital
Mallinckrodt Institute of Radiology

510 South Kingshighway Boulevard
St. Louis, MO 63110

Suite: West Pavillion, 956
Office Phone: 314-362-1952

Education

Education

Fellowship: Nuclear Medicine, University of Michigan Hospitals, Ann Arbor, Michigan 1986
Residency: Internal Medicine, University of Michigan Hospitals, Ann Arbor, Michigan 1984
Medical Degree: Stanford University School of Medicine, Stanford, California 1981
M.S.: Computer Science, Stanford University, Stanford, California 1981

Publication & Research

Publication & Research

Fetal Radiation Dose from 18F-FDG in Pregnant Patients Imaged with PET, PET/CT, and PET/MR.
Zanotti-Fregonara P, Laforest R, Wallis JW
J Nucl Med. 2015 Aug; 56(8)1218-22. doi: 10.2967/jnumed.115.157032.

PMID:
    26089550
    [PubMed - indexed for MEDLINE]
Related citations


Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.
Delaneau O, Marchini J, 1000 Genomes Project Consortium., 1000 Genomes Project Consortium.
Nat Commun. 2014 Jun 13; 53934. doi: 10.1038/ncomms4934.

PMID:
    25653097
    [PubMed - indexed for MEDLINE]
Related citations


Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences.
Colonna V, Ayub Q, Chen Y, Pagani L, Luisi P, Pybus M, Garrison E, Xue Y, Tyler-Smith C, 1000 Genomes Project Consortium., Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA
Genome Biol. 2014 Jun 30; 15(6)R88. doi: 10.1186/gb-2014-15-6-r88.

PMID:
    24980144
    [PubMed - indexed for MEDLINE]
Related citations


The SNMMI and EANM practice guideline for tele-nuclear medicine 2.0.
Parker JA, Christian P, Jadvar H, Sattler B, Wallis JW
J Nucl Med Technol. 2014 Mar; 42(1)15-9. doi: 10.2967/jnmt.113.133231.

PMID:
    24375155
    [PubMed - indexed for MEDLINE]
Related citations


Integrative annotation of variants from 1092 humans: application to cancer genomics.
Khurana E, Fu Y, Colonna V, Mu XJ, Kang HM, Lappalainen T, Sboner A, Lochovsky L, Chen J, Harmanci A, Das J, Abyzov A, Balasubramanian S, Beal K, Chakravarty D, Challis D, Chen Y, Clarke D, Clarke L, Cunningham F, Evani US, Flicek P, Fragoza R, Garrison E, Gibbs R, Gümüş ZH, Herrero J, Kitabayashi N, Kong Y, Lage K, Liluashvili V, Lipkin SM, MacArthur DG, Marth G, Muzny D, Pers TH, Ritchie GRS, Rosenfeld JA, Sisu C, Wei X, Wilson M, Xue Y, Yu F, 1000 Genomes Project Consortium., Dermitzakis ET, Yu H, Rubin MA, Tyler-Smith C, Gerstein M
Science. 2013 Oct 4; 342(6154)1235587. doi: 10.1126/science.1235587.

PMID:
    24092746
    [PubMed - indexed for MEDLINE]
Related citations


The Cancer Genome Atlas Pan-Cancer analysis project.
Cancer Genome Atlas Research Network., Weinstein JN, Collisson EA, Mills GB, Shaw KR, Ozenberger BA, Ellrott K, Shmulevich I, Sander C, Stuart JM
Nat Genet. 2013 Oct; 45(10)1113-20. doi: 10.1038/ng.2764.

PMID:
    24071849
    [PubMed - indexed for MEDLINE]
Related citations


BreakTrans: uncovering the genomic architecture of gene fusions.
Chen K, Navin NE, Wang Y, Schmidt HK, Wallis JW, Niu B, Fan X, Zhao H, McLellan MD, Hoadley KA, Mardis ER, Ley TJ, Perou CM, Wilson RK, Ding L
Genome Biol. 2013 Aug 23; 14(8)R87. doi: 10.1186/gb-2013-14-8-r87.

PMID:
    23972288
    [PubMed - indexed for MEDLINE]
Related citations


Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.
Cancer Genome Atlas Research Network., Ley TJ, Miller C, Ding L, Raphael BJ, Mungall AJ, Robertson A, Hoadley K, Triche TJ Jr, Laird PW, Baty JD, Fulton LL, Fulton R, Heath SE, Kalicki-Veizer J, Kandoth C, Klco JM, Koboldt DC, Kanchi KL, Kulkarni S, Lamprecht TL, Larson DE, Lin L, Lu C, McLellan MD, McMichael JF, Payton J, Schmidt H, Spencer DH, Tomasson MH, Wallis JW, Wartman LD, Watson MA, Welch J, Wendl MC, Ally A, Balasundaram M, Birol I, Butterfield Y, Chiu R, Chu A, Chuah E, Chun HJ, Corbett R, Dhalla N, Guin R, He A, Hirst C, Hirst M, Holt RA, Jones S, Karsan A, Lee D, Li HI, Marra MA, Mayo M, Moore RA, Mungall K, Parker J, Pleasance E, Plettner P, Schein J, Stoll D, Swanson L, Tam A, Thiessen N, Varhol R, Wye N, Zhao Y, Gabriel S, Getz G, Sougnez C, Zou L, Leiserson MD, Vandin F, Wu HT, Applebaum F, Baylin SB, Akbani R, Broom BM, Chen K, Motter TC, Nguyen K, Weinstein JN, Zhang N, Ferguson ML, Adams C, Black A, Bowen J, Gastier-Foster J, Grossman T, Lichtenberg T, Wise L, Davidsen T, Demchok JA, Shaw KR, Sheth M, Sofia HJ, Yang L, Downing JR, Eley G
N Engl J Med. 2013 May 30; 368(22)2059-74. doi: 10.1056/NEJMoa1301689.

PMID:
    23634996
    [PubMed - indexed for MEDLINE]
Related citations


Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma.
Gutmann DH, McLellan MD, Hussain I, Wallis JW, Fulton LL, Fulton RS, Magrini V, Demeter R, Wylie T, Kandoth C, Leonard JR, Guha A, Miller CA, Ding L, Mardis ER
Genome Res. 2013 Mar; 23(3)431-9. doi: 10.1101/gr.142604.112.

PMID:
    23222849
    [PubMed - indexed for MEDLINE]
Related citations


An integrated map of genetic variation from 1,092 human genomes.
1000 Genomes Project Consortium., Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA
Nature. 2012 Nov 1; 491(7422)56-65. doi: 10.1038/nature11632.

PMID:
    23128226
    [PubMed - indexed for MEDLINE]
Related citations


The origin and evolution of mutations in acute myeloid leukemia.
Welch JS, Ley TJ, Link DC, Miller CA, Larson DE, Koboldt DC, Wartman LD, Lamprecht TL, Liu F, Xia J, Kandoth C, Fulton RS, McLellan MD, Dooling DJ, Wallis JW, Chen K, Harris CC, Schmidt HK, Kalicki-Veizer JM, Lu C, Zhang Q, Lin L, O'Laughlin MD, McMichael JF, Delehaunty KD, Fulton LA, Magrini VJ, McGrath SD, Demeter RT, Vickery TL, Hundal J, Cook LL, Swift GW, Reed JP, Alldredge PA, Wylie TN, Walker JR, Watson MA, Heath SE, Shannon WD, Varghese N, Nagarajan R, Payton JE, Baty JD, Kulkarni S, Klco JM, Tomasson MH, Westervelt P, Walter MJ, Graubert TA, DiPersio JF, Ding L, Mardis ER, Wilson RK
Cell. 2012 Jul 20; 150(2)264-78. doi: 10.1016/j.cell.2012.06.023.

PMID:
    22817890
    [PubMed - indexed for MEDLINE]
Related citations


Whole-genome analysis informs breast cancer response to aromatase inhibition.
Ellis MJ, Ding L, Shen D, Luo J, Suman VJ, Wallis JW, Van Tine BA, Hoog J, Goiffon RJ, Goldstein TC, Ng S, Lin L, Crowder R, Snider J, Ballman K, Weber J, Chen K, Koboldt DC, Kandoth C, Schierding WS, McMichael JF, Miller CA, Lu C, Harris CC, McLellan MD, Wendl MC, DeSchryver K, Allred DC, Esserman L, Unzeitig G, Margenthaler J, Babiera GV, Marcom PK, Guenther JM, Leitch M, Hunt K, Olson J, Tao Y, Maher CA, Fulton LL, Fulton RS, Harrison M, Oberkfell B, Du F, Demeter R, Vickery TL, Elhammali A, Piwnica-Worms H, McDonald S, Watson M, Dooling DJ, Ota D, Chang LW, Bose R, Ley TJ, Piwnica-Worms D, Stuart JM, Wilson RK, Mardis ER
Nature. 2012 Jun 10; 486(7403)353-60. doi: 10.1038/nature11143.

PMID:
    22722193
    [PubMed - indexed for MEDLINE]
Related citations


BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data.
Chen K, Wallis JW, Kandoth C, Kalicki-Veizer JM, Mungall KL, Mungall AJ, Jones SJ, Marra MA, Ley TJ, Mardis ER, Wilson RK, Weinstein JN, Ding L
Bioinformatics. 2012 Jul 15; 28(14)1923-4. doi: 10.1093/bioinformatics/bts272.

PMID:
    22563071
    [PubMed - indexed for MEDLINE]
Related citations


The 1000 Genomes Project: data management and community access.
Clarke L, Zheng-Bradley X, Smith R, Kulesha E, Xiao C, Toneva I, Vaughan B, Preuss D, Leinonen R, Shumway M, Sherry S, Flicek P, 1000 Genomes Project Consortium.
Nat Methods. 2012 Apr 27; 9(5)459-62. doi: 10.1038/nmeth.1974.

PMID:
    22543379
    [PubMed - indexed for MEDLINE]
Related citations


SNM practice guideline for lung scintigraphy 4.0.
Parker JA, Coleman RE, Grady E, Royal HD, Siegel BA, Stabin MG, Sostman HD, Hilson AJ, Society of Nuclear Medicine.
J Nucl Med Technol. 2012 Mar; 40(1)57-65. doi: 10.2967/jnmt.111.101386.

PMID:
    22282651
    [PubMed - indexed for MEDLINE]
Related citations


Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing.
Ding L, Ley TJ, Larson DE, Miller CA, Koboldt DC, Welch JS, Ritchey JK, Young MA, Lamprecht T, McLellan MD, McMichael JF, Wallis JW, Lu C, Shen D, Harris CC, Dooling DJ, Fulton RS, Fulton LL, Chen K, Schmidt H, Kalicki-Veizer J, Magrini VJ, Cook L, McGrath SD, Vickery TL, Wendl MC, Heath S, Watson MA, Link DC, Tomasson MH, Shannon WD, Payton JE, Kulkarni S, Westervelt P, Walter MJ, Graubert TA, Mardis ER, Wilson RK, DiPersio JF
Nature. 2012 Jan 11; 481(7382)506-10. doi: 10.1038/nature10738.

PMID:
    22237025
    [PubMed - indexed for MEDLINE]
Related citations


The SNM practice guideline for somatostatin receptor scintigraphy 2.0.
Balon HR, Brown TL, Goldsmith SJ, Silberstein EB, Krenning EP, Lang O, Dillehay G, Tarrance J, Johnson M, Stabin MG, Society of Nuclear Medicine.
J Nucl Med Technol. 2011 Dec; 39(4)317-24. doi: 10.2967/jnmt.111.098277.

PMID:
    22068564
    [PubMed - indexed for MEDLINE]
Related citations


The functional spectrum of low-frequency coding variation.
Marth GT, Yu F, Indap AR, Garimella K, Gravel S, Leong WF, Tyler-Smith C, Bainbridge M, Blackwell T, Zheng-Bradley X, Chen Y, Challis D, Clarke L, Ball EV, Cibulskis K, Cooper DN, Fulton B, Hartl C, Koboldt D, Muzny D, Smith R, Sougnez C, Stewart C, Ward A, Yu J, Xue Y, Altshuler D, Bustamante CD, Clark AG, Daly M, DePristo M, Flicek P, Gabriel S, Mardis E, Palotie A, Gibbs R, 1000 Genomes Project.
Genome Biol. 2011 Sep 14; 12(9)R84. doi: 10.1186/gb-2011-12-9-r84.

PMID:
    21917140
    [PubMed - indexed for MEDLINE]
Related citations


Demographic history and rare allele sharing among human populations.
Gravel S, Henn BM, Gutenkunst RN, Indap AR, Marth GT, Clark AG, Yu F, Gibbs RA, 1000 Genomes Project., Bustamante CD
Proc Natl Acad Sci U S A. 2011 Jul 19; 108(29)11983-8. doi: 10.1073/pnas.1019276108.

PMID:
    21730125
    [PubMed - indexed for MEDLINE]
Related citations


Variation in genome-wide mutation rates within and between human families.
Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, Hurles ME, Awadalla P, 1000 Genomes Project.
Nat Genet. 2011 Jun 12; 43(7)712-4. doi: 10.1038/ng.862.

PMID:
    21666693
    [PubMed - indexed for MEDLINE]
Related citations

Areas of Research Interest

Computer applications in nuclear medicine