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Anne Marie Comeau PhD

TitleProfessor
InstitutionUMass Chan Medical School
DepartmentPediatrics
Address305 South Street
Jamaica Plain MA 02130
Phone774-455-4600
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    Other Positions
    InstitutionT.H. Chan School of Medicine
    DepartmentPediatrics
    DivisionPediatric Genetics


    Collapse Biography 
    Collapse education and training
    College of the Holy Cross, Worcester, MA, United StatesBALiberal Arts
    Brandeis University, Waltham, MA, United StatesPHDBiology

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Ma KC, Hale JE, Grad YH, Alter G, Luzuriaga K, Eaton RB, Fischinger S, Kaur D, Brody R, Siddiqui SM, Leach D, Brown CM, Klevens RM, Madoff L, Comeau AM. Trends in Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Seroprevalence in Massachusetts Estimated from Newborn Screening Specimens. Clin Infect Dis. 2022 08 24; 75(1):e105-e113. PMID: 35213690.
      Citations:    Fields:    
    2. Kumar B, Barton S, Kordowska J, Eaton RB, Counihan AM, Hale JE, Comeau AM. Novel Modification of a Confirmatory SMA Sequencing Assay that Can Be Used to Determine SMN2 Copy Number. Int J Neonatal Screen. 2021 Jul 21; 7(3). PMID: 34449530.
      Citations:    
    3. Hale JE, Darras BT, Swoboda KJ, Estrella E, Chen JYH, Abbott MA, Hay BN, Kumar B, Counihan AM, Gerstel-Thompson J, Sahai I, Eaton RB, Comeau AM. Massachusetts' Findings from Statewide Newborn Screening for Spinal Muscular Atrophy. Int J Neonatal Screen. 2021 May 23; 7(2). PMID: 34071063.
      Citations:    
    4. Hale JE, Platt CD, Bonilla FA, Hay BN, Sullivan JL, Johnston AM, Pasternack MS, Hesterberg PE, Meissner HC, Cooper ER, Barmettler S, Farmer JR, Fisher D, Walter JE, Yang NJ, Sahai I, Eaton RB, DeMaria A, Notarangelo LD, Pai SY, Comeau AM. Ten Years of Newborn Screening for Severe Combined Immunodeficiency (SCID) in Massachusetts. J Allergy Clin Immunol Pract. 2021 05; 9(5):2060-2067.e2. PMID: 33607339.
      Citations: 4     Fields:    Translation:HumansPHPublic Health
    5. Verheijen J, Wong SY, Rowe JH, Raymond K, Stoddard J, Delmonte OM, Bosticardo M, Dobbs K, Niemela J, Calzoni E, Pai SY, Choi U, Yamazaki Y, Comeau AM, Janssen E, Henderson L, Hazen M, Berry G, Rosenzweig SD, Aldhekri HH, He M, Notarangelo LD, Morava E. Defining a new immune deficiency syndrome: MAN2B2-CDG. J Allergy Clin Immunol. 2020 03; 145(3):1008-1011. PMID: 31775018.
      Citations: 5     Fields:    Translation:HumansCells
    6. Purswani P, Meehan CA, Kuehn HS, Chang Y, Dasso JF, Meyer AK, Ujhazi B, Csomos K, Lindsay D, Alberdi T, Joychan S, Trotter J, Duff C, Ellison M, Bleesing J, Kumanovics A, Comeau AM, Hale JE, Notarangelo LD, Torgersen TR, Ochs HD, Sriaroon P, Oshrine B, Petrovic A, Rosenzweig SD, Leiding JW, Walter JE. Two Unique Cases of X-linked SCID: A Diagnostic Challenge in the Era of Newborn Screening. Front Pediatr. 2019; 7:55. PMID: 31024866.
      Citations:    
    7. Comeau AM. Paradigm shifts in newborn screening? Genet Med. 2019 03; 21(3):534-535. PMID: 30093708.
      Citations: 1     Fields:    Translation:HumansPHPublic Health
    8. Sontag MK, Sarkar D, Comeau AM, Hassell K, Botto LD, Parad R, Rose SR, Wintergerst KA, Smith-Whitley K, Singh S, Yusuf C, Ojodu J, Copeland S, Hinton CF. Case Definitions for Conditions Identified by Newborn Screening Public Health Surveillance. Int J Neonatal Screen. 2018; 4(2):16. PMID: 29862374.
      Citations:    
    9. Goda V, Malik A, Kalmar T, Maroti Z, Patel B, Ujhazi B, Csomos K, Hale JE, Chen K, Bleesing J, Palma P, Cancrini C, Comeau AM, Krivan G, Walter JE. Partial RAG deficiency in a patient with varicella infection, autoimmune cytopenia, and anticytokine antibodies. J Allergy Clin Immunol Pract. 2018 Sep - Oct; 6(5):1769-1771.e2. PMID: 29410113.
      Citations: 11     Fields:    Translation:HumansCells
    10. Delmonte OM, Biggs CM, Hayward A, Comeau AM, Kuehn HS, Rosenzweig SD, Notarangelo LD. First Case of X-Linked Moesin Deficiency Identified After Newborn Screening for SCID. J Clin Immunol. 2017 05; 37(4):336-338. PMID: 28378256.
      Citations: 10     Fields:    Translation:HumansPHPublic Health
    11. Kemper AR, Brosco J, Comeau AM, Green NS, Grosse SD, Jones E, Kwon JM, Lam WK, Ojodu J, Prosser LA, Tanksley S. Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation. Genet Med. 2017 01; 19(1):121-126. PMID: 27337030.
      Citations: 37     Fields:    Translation:HumansPHPublic Health
    12. Brauer PM, Pessach IM, Clarke E, Rowe JH, Ott de Bruin L, Lee YN, Dominguez-Brauer C, Comeau AM, Awong G, Felgentreff K, Zhang YH, Bredemeyer A, Al-Herz W, Du L, Ververs F, Kennedy M, Giliani S, Keller G, Sleckman BP, Schatz DG, Bushman FD, Notarangelo LD, Zúñiga-Pflücker JC. Modeling altered T-cell development with induced pluripotent stem cells from patients with RAG1-dependent immune deficiencies. Blood. 2016 08 11; 128(6):783-93. PMID: 27301863.
      Citations: 17     Fields:    Translation:HumansCells
    13. Hinton CF, Homer CJ, Thompson AA, Williams A, Hassell KL, Feuchtbaum L, Berry SA, Comeau AM, Therrell BL, Brower A, Harris KB, Brown C, Monaco J, Ostrander RJ, Zuckerman AE, Kaye C, Dougherty D, Greene C, Green NS. A framework for assessing outcomes from newborn screening: on the road to measuring its promise. Mol Genet Metab. 2016 08; 118(4):221-9. PMID: 27268406.
      Citations: 11     Fields:    Translation:HumansPHPublic Health
    14. Goldenberg AJ, Comeau AM, Grosse SD, Tanksley S, Prosser LA, Ojodu J, Botkin JR, Kemper AR, Green NS. Evaluating Harms in the Assessment of Net Benefit: A Framework for Newborn Screening Condition Review. Matern Child Health J. 2016 Mar; 20(3):693-700. PMID: 26833040.
      Citations: 16     Fields:    Translation:HumansPHPublic Health
    15. Allan GM, Lindblad AJ, Comeau A, Coppola J, Hudson B, Mannarino M, McMinis C, Padwal R, Schelstraete C, Zarnke K, Garrison S, Cotton C, Korownyk C, McCormack J, Nickel S, Kolber MR. Simplified lipid guidelines: Prevention and management of cardiovascular disease in primary care. Can Fam Physician. 2015 Oct; 61(10):857-67, e439-50. PMID: 26472792.
      Citations: 39     Fields:    Translation:HumansPHPublic Health
    16. Dobbs K, Domínguez Conde C, Zhang SY, Parolini S, Audry M, Chou J, Haapaniemi E, Keles S, Bilic I, Okada S, Massaad MJ, Rounioja S, Alwahadneh AM, Serwas NK, Capuder K, Çiftçi E, Felgentreff K, Ohsumi TK, Pedergnana V, Boisson B, Haskolo?lu ?, Ensari A, Schuster M, Moretta A, Itan Y, Patrizi O, Rozenberg F, Lebon P, Saarela J, Knip M, Petrovski S, Goldstein DB, Parrott RE, Savas B, Schambach A, Tabellini G, Bock C, Chatila TA, Comeau AM, Geha RS, Abel L, Buckley RH, ?kincio?ullar? A, Al-Herz W, Helminen M, Do?u F, Casanova JL, Boztu? K, Notarangelo LD. Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections. N Engl J Med. 2015 Jun 18; 372(25):2409-22. PMID: 26083206.
      Citations: 78     Fields:    Translation:HumansCells
    17. Kwan A, Abraham RS, Currier R, Brower A, Andruszewski K, Abbott JK, Baker M, Ballow M, Bartoshesky LE, Bonilla FA, Brokopp C, Brooks E, Caggana M, Celestin J, Church JA, Comeau AM, Connelly JA, Cowan MJ, Cunningham-Rundles C, Dasu T, Dave N, De La Morena MT, Duffner U, Fong CT, Forbes L, Freedenberg D, Gelfand EW, Hale JE, Hanson IC, Hay BN, Hu D, Infante A, Johnson D, Kapoor N, Kay DM, Kohn DB, Lee R, Lehman H, Lin Z, Lorey F, Abdel-Mageed A, Manning A, McGhee S, Moore TB, Naides SJ, Notarangelo LD, Orange JS, Pai SY, Porteus M, Rodriguez R, Romberg N, Routes J, Ruehle M, Rubenstein A, Saavedra-Matiz CA, Scott G, Scott PM, Secord E, Seroogy C, Shearer WT, Siegel S, Silvers SK, Stiehm ER, Sugerman RW, Sullivan JL, Tanksley S, Tierce ML, Verbsky J, Vogel B, Walker R, Walkovich K, Walter JE, Wasserman RL, Watson MS, Weinberg GA, Weiner LB, Wood H, Yates AB, Puck JM, Bonagura VR. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States. JAMA. 2014 Aug 20; 312(7):729-38. PMID: 25138334.
      Citations: 210     Fields:    Translation:HumansCellsPHPublic Health
    18. Botkin JR, Lewis MH, Watson MS, Swoboda KJ, Anderson R, Berry SA, Bonhomme N, Brosco JP, Comeau AM, Goldenberg A, Goldman E, Therrell B, Levy-Fisch J, Tarini B, Wilfond B. Parental permission for pilot newborn screening research: guidelines from the NBSTRN. Pediatrics. 2014 Feb; 133(2):e410-7. PMID: 24394680.
      Citations: 13     Fields:    Translation:HumansPHPublic Health
    19. Kemper AR, Green NS, Calonge N, Lam WK, Comeau AM, Goldenberg AJ, Ojodu J, Prosser LA, Tanksley S, Bocchini JA. Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children. Genet Med. 2014 Feb; 16(2):183-7. PMID: 23907646.
      Citations: 44     Fields:    Translation:HumansPHPublic Health
    20. Chen R, Giliani S, Lanzi G, Mias GI, Lonardi S, Dobbs K, Manis J, Im H, Gallagher JE, Phanstiel DH, Euskirchen G, Lacroute P, Bettinger K, Moratto D, Weinacht K, Montin D, Gallo E, Mangili G, Porta F, Notarangelo LD, Pedretti S, Al-Herz W, Alfahdli W, Comeau AM, Traister RS, Pai SY, Carella G, Facchetti F, Nadeau KC, Snyder M, Notarangelo LD. Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias. J Allergy Clin Immunol. 2013 Sep; 132(3):656-664.e17. PMID: 23830146.
      Citations: 59     Fields:    Translation:HumansAnimals
    21. Henderson LA, Frugoni F, Hopkins G, Al-Herz W, Weinacht K, Comeau AM, Bonilla FA, Notarangelo LD, Pai SY. First reported case of Omenn syndrome in a patient with reticular dysgenesis. J Allergy Clin Immunol. 2013 Apr; 131(4):1227-30, 1230.e1-3. PMID: 23014587.
      Citations: 12     Fields:    Translation:HumansCells
    22. Punwani D, Gonzalez-Espinosa D, Comeau AM, Dutra A, Pak E, Puck J. Cellular calibrators to quantitate T-cell receptor excision circles (TRECs) in clinical samples. Mol Genet Metab. 2012 Nov; 107(3):586-91. PMID: 23062576.
      Citations: 2     Fields:    Translation:HumansCellsPHPublic Health
    23. Kemper AR, Kus CA, Ostrander RJ, Comeau AM, Boyle CA, Dougherty D, Mann MY, Botkin JR, Green NS. A framework for key considerations regarding point-of-care screening of newborns. Genet Med. 2012 Dec; 14(12):951-4. PMID: 22899090.
      Citations: 4     Fields:    Translation:HumansPHPublic Health
    24. Kemper AR, Knapp AA, Metterville DR, Comeau AM, Green NS, Perrin JM. Weighing the evidence for newborn screening for Hemoglobin H disease. J Pediatr. 2011 May; 158(5):780-3. PMID: 21167500.
      Citations: 1     Fields:    Translation:HumansPHPublic Health
    25. Sahai I, Eaton RB, Hale JE, Mulcahy EA, Comeau AM. Long-term follow-up to ensure quality care of individuals diagnosed with newborn screening conditions: early experience in New England. Genet Med. 2010 Dec; 12(12 Suppl):S220-7. PMID: 21150368.
      Citations: 4     Fields:    Translation:HumansPHPublic Health
    26. Hale JE, Bonilla FA, Pai SY, Gerstel-Thompson JL, Notarangelo LD, Eaton RB, Comeau AM. Identification of an infant with severe combined immunodeficiency by newborn screening. J Allergy Clin Immunol. 2010 Nov; 126(5):1073-4. PMID: 20933257.
      Citations: 27     Fields:    Translation:HumansPHPublic Health
    27. Kemper AR, Knapp AA, Green NS, Comeau AM, Metterville DR, Perrin JM. Weighing the evidence for newborn screening for early-infantile Krabbe disease. Genet Med. 2010 Sep; 12(9):539-43. PMID: 20601893.
      Citations: 20     Fields:    Translation:HumansPHPublic Health
    28. Gerstel-Thompson JL, Wilkey JF, Baptiste JC, Navas JS, Pai SY, Pass KA, Eaton RB, Comeau AM. High-throughput multiplexed T-cell-receptor excision circle quantitative PCR assay with internal controls for detection of severe combined immunodeficiency in population-based newborn screening. Clin Chem. 2010 Sep; 56(9):1466-74. PMID: 20660142.
      Citations: 47     Fields:    Translation:HumansPHPublic Health
    29. Janik DK, Lindau-Shepard B, Comeau AM, Pass KA. A multiplex immunoassay using the Guthrie specimen to detect T-cell deficiencies including severe combined immunodeficiency disease. Clin Chem. 2010 Sep; 56(9):1460-5. PMID: 20660143.
      Citations: 11     Fields:    Translation:HumansCells
    30. Hale JE, Parad RB, Dorkin HL, Gerstle R, Lapey A, O'Sullivan BP, Spencer T, Yee W, Comeau AM. Cystic fibrosis newborn screening: using experience to optimize the screening algorithm. J Inherit Metab Dis. 2010 Oct; 33(Suppl 2):S255-61. PMID: 20521170.
      Citations: 5     Fields:    Translation:HumansPHPublic Health
    31. Comeau AM, Hale JE, Pai SY, Bonilla FA, Notarangelo LD, Pasternack MS, Meissner HC, Cooper ER, DeMaria A, Sahai I, Eaton RB. Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency. J Inherit Metab Dis. 2010 Oct; 33(Suppl 2):S273-81. PMID: 20490925.
      Citations: 28     Fields:    Translation:HumansPHPublic Health
    32. Perrin JM, Knapp AA, Browning MF, Comeau AM, Green NS, Lipstein EA, Metterville DR, Prosser L, Queally D, Kemper AR. An evidence development process for newborn screening. Genet Med. 2010 Mar; 12(3):131-4. PMID: 20154629.
      Citations: 10     Fields:    Translation:HumansPHPublic Health
    33. Carlson D, McKeen E, Mitchell M, Torres B, Parad R, Comeau AM, O'Sullivan BP. Oropharyngeal flora in healthy infants: observations and implications for cystic fibrosis care. Pediatr Pulmonol. 2009 May; 44(5):497-502. PMID: 19360845.
      Citations: 3     Fields:    Translation:HumansCells
    34. Ngo-Giang-Huong N, Khamduang W, Leurent B, Collins I, Nantasen I, Leechanachai P, Sirirungsi W, Limtrakul A, Leusaree T, Comeau AM, Lallemant M, Jourdain G. Early HIV-1 diagnosis using in-house real-time PCR amplification on dried blood spots for infants in remote and resource-limited settings. J Acquir Immune Defic Syndr. 2008 Dec 15; 49(5):465-71. PMID: 18989220.
      Citations: 19     Fields:    Translation:HumansCellsPHPublic Health
    35. Hsu HW, Zytkovicz TH, Comeau AM, Strauss AW, Marsden D, Shih VE, Grady GF, Eaton RB. Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening. Pediatrics. 2008 May; 121(5):e1108-14. PMID: 18450854.
      Citations: 19     Fields:    Translation:HumansPHPublic Health
    36. Hale JE, Parad RB, Comeau AM. Newborn screening showing decreasing incidence of cystic fibrosis. N Engl J Med. 2008 Feb 28; 358(9):973-4. PMID: 18305279.
      Citations: 16     Fields:    Translation:HumansPHPublic Health
    37. Comeau AM, Accurso FJ, White TB, Campbell PW, Hoffman G, Parad RB, Wilfond BS, Rosenfeld M, Sontag MK, Massie J, Farrell PM, O'Sullivan BP. Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report. Pediatrics. 2007 Feb; 119(2):e495-518. PMID: 17272609.
      Citations: 39     Fields:    Translation:HumansPHPublic Health
    38. O'Sullivan BP, Zwerdling RG, Dorkin HL, Comeau AM, Parad R. Early pulmonary manifestation of cystic fibrosis in children with the DeltaF508/R117H-7T genotype. Pediatrics. 2006 Sep; 118(3):1260-5. PMID: 16951024.
      Citations: 9     Fields:    Translation:HumansCellsPHPublic Health
    39. Pass K, Green NS, Lorey F, Sherwin J, Comeau AM. Pilot programs in newborn screening. Ment Retard Dev Disabil Res Rev. 2006; 12(4):293-300. PMID: 17183570.
      Citations: 7     Fields:    Translation:HumansPHPublic Health
    40. Parad RB, Comeau AM, Dorkin HL, Dovey M, Gerstle R, Martin T, O'Sullivan BP. Sweat testing infants detected by cystic fibrosis newborn screening. J Pediatr. 2005 Sep; 147(3 Suppl):S69-72. PMID: 16202787.
      Citations: 12     Fields:    Translation:HumansPHPublic Health
    41. Parad RB, Comeau AM. Diagnostic dilemmas resulting from the immunoreactive trypsinogen/DNA cystic fibrosis newborn screening algorithm. J Pediatr. 2005 Sep; 147(3 Suppl):S78-82. PMID: 16202789.
      Citations: 7     Fields:    Translation:HumansPHPublic Health
    42. Comeau AM, Parad R, Gerstle R, O'Sullivan BP, Dorkin HL, Dovey M, Haver K, Martin T, Eaton RB. Challenges in implementing a successful newborn cystic fibrosis screening program. J Pediatr. 2005 Sep; 147(3 Suppl):S89-93. PMID: 16202791.
      Citations: 2     Fields:    Translation:HumansPHPublic Health
    43. Comeau AM, Parad R, Gerstle R, O'Sullivan BP, Dorkin HL, Dovey M, Haver K, Martin T, Eaton RB. Communications systems and their models: Massachusetts parent compliance with recommended specialty care after positive cystic fibrosis newborn screening result. J Pediatr. 2005 Sep; 147(3 Suppl):S98-100. PMID: 16202793.
      Citations: 4     Fields:    Translation:HumansPHPublic Health
    44. Grosse SD, Boyle CA, Botkin JR, Comeau AM, Kharrazi M, Rosenfeld M, Wilfond BS. Newborn screening for cystic fibrosis: evaluation of benefits and risks and recommendations for state newborn screening programs. MMWR Recomm Rep. 2004 Oct 15; 53(RR-13):1-36. PMID: 15483524.
      Citations: 74     Fields:    Translation:HumansPHPublic Health
    45. Comeau AM, Parad RB, Dorkin HL, Dovey M, Gerstle R, Haver K, Lapey A, O'Sullivan BP, Waltz DA, Zwerdling RG, Eaton RB. Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections. Pediatrics. 2004 Jun; 113(6):1573-81. PMID: 15173476.
      Citations: 39     Fields:    Translation:HumansPHPublic Health
    46. Comeau AM, Larson C, Eaton RB. Integration of new genetic diseases into statewide newborn screening: New England experience. Am J Med Genet C Semin Med Genet. 2004 Feb 15; 125C(1):35-41. PMID: 14755432.
      Citations: 6     Fields:    Translation:HumansPHPublic Health
    47. Parad RB, Comeau AM. Newborn screening for cystic fibrosis. Pediatr Ann. 2003 Aug; 32(8):528-35. PMID: 12942895.
      Citations: 2     Fields:    Translation:HumansPHPublic Health
    48. Brambilla D, Jennings C, Aldrovandi G, Bremer J, Comeau AM, Cassol SA, Dickover R, Jackson JB, Pitt J, Sullivan JL, Butcher A, Grosso L, Reichelderfer P, Fiscus SA. Multicenter evaluation of use of dried blood and plasma spot specimens in quantitative assays for human immunodeficiency virus RNA: measurement, precision, and RNA stability. J Clin Microbiol. 2003 May; 41(5):1888-93. PMID: 12734222.
      Citations: 46     Fields:    Translation:HumansCells
    49. Comeau AM, Eaton RB. Successes of newborn screening programs. Science. 2002 Jan 04; 295(5552):44-5. PMID: 11780647.
      Citations: 1     Fields:    Translation:HumansPHPublic Health
    50. Eaton RB, Comeau AM, Zytkovicz TH, Larson C. Newborn screening: new developments in a proven field. Clin Lab Sci. 2002; 15(4):239-44. PMID: 12776784.
      Citations:    Fields:    Translation:HumansPHPublic Health
    51. Zytkovicz TH, Fitzgerald EF, Marsden D, Larson CA, Shih VE, Johnson DM, Strauss AW, Comeau AM, Eaton RB, Grady GF. Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program. Clin Chem. 2001 Nov; 47(11):1945-55. PMID: 11673361.
      Citations: 126     Fields:    Translation:HumansPHPublic Health
    52. Wheeler PG, Smith R, Dorkin H, Parad RB, Comeau AM, Bianchi DW. Genetic counseling after implementation of statewide cystic fibrosis newborn screening: Two years' experience in one medical center. Genet Med. 2001 Nov-Dec; 3(6):411-5. PMID: 11715005.
      Citations: 9     Fields:    Translation:HumansPHPublic Health
    53. Lallemant M, Jourdain G, Le Coeur S, Kim S, Koetsawang S, Comeau AM, Phoolcharoen W, Essex M, McIntosh K, Vithayasai V. A trial of shortened zidovudine regimens to prevent mother-to-child transmission of human immunodeficiency virus type 1. Perinatal HIV Prevention Trial (Thailand) Investigators. N Engl J Med. 2000 Oct 05; 343(14):982-91. PMID: 11018164.
      Citations: 84     Fields:    Translation:HumansPHPublic HealthCTClinical Trials
    54. Su X, Comeau AM. Cellulose as a matrix for nucleic acid purification. Anal Biochem. 1999 Feb 15; 267(2):415-8. PMID: 10036150.
      Citations: 11     Fields:    
    55. Canosa CA, Grady GF, Cabello ML, Comeau AM, Schwerzler ME, Contreras MT, Fraga JM, Gomez de los Terreros I, Pena J. Anonymous testing of newborn infants for HIV antibodies as a basis for estimating prevalence of HIV in childbearing women: the 1991-1994 study in Spain. Acta Paediatr Suppl. 1997 Jun; 421:67-71. PMID: 9240862.
      Citations: 1     Fields:    Translation:HumansCellsPHPublic Health
    56. Su X, Mushinsky G, Comeau AM. A cost effective base-matching assay with low backgrounds. Nucleic Acids Res. 1996 Nov 15; 24(22):4596-7. PMID: 8948656.
      Citations:    Fields:    Translation:Humans
    57. Comeau AM, Pitt J, Hillyer GV, Landesman S, Bremer J, Chang BH, Lew J, Moye J, Grady GF, McIntosh K. Early detection of human immunodeficiency virus on dried blood spot specimens: sensitivity across serial specimens. Women and Infants Transmission Study Group. J Pediatr. 1996 Jul; 129(1):111-8. PMID: 8757570.
      Citations: 21     Fields:    Translation:HumansCells
    58. McIntosh K, Comeau AM, Wara D, Diaz C, Landesman S, Pitt J, Rich K, Lew J, Moye J, Kalish LA. The utility of IgA antibody to human immunodeficiency virus type 1 in early diagnosis of vertically transmitted infection. National Institute of Allergy and Infectious Diseases and National Institute of Child Health and Human Development Women and Infants Transmission Study Group. Arch Pediatr Adolesc Med. 1996 Jun; 150(6):598-602. PMID: 8646309.
      Citations:    Fields:    Translation:HumansCellsPHPublic HealthCTClinical Trials
    59. Comeau AM. Application of the polymerase chain reaction for the detection of HIV in specimens from newborn screening programs. Acta Paediatr Suppl. 1994 Aug; 400:29-30. PMID: 7833556.
      Citations:    Fields:    Translation:HumansPHPublic Health
    60. Comeau AM, Hsu HW, Schwerzler M, Mushinsky G, Walter E, Hofman L, Grady GF. Identifying human immunodeficiency virus infection at birth: application of polymerase chain reaction to Guthrie cards. J Pediatr. 1993 Aug; 123(2):252-8. PMID: 8345421.
      Citations: 11     Fields:    Translation:HumansCells
    61. Comeau AM, Hsu HW, Schwerzler M, Mushinsky G, Grady GF. Detection of HIV in specimens from newborn screening programs. N Engl J Med. 1992 Jun 18; 326(25):1703. PMID: 1588991.
      Citations: 4     Fields:    Translation:HumansCellsPHPublic Health
    62. Comeau AM, Harris JA, McIntosh K, Weiblen BJ, Hoff R, Grady GF. Polymerase chain reaction in detecting HIV infection among seropositive infants: relation to clinical status and age and to results of other assays. J Acquir Immune Defic Syndr (1988). 1992; 5(3):271-8. PMID: 1740753.
      Citations: 9     Fields:    Translation:HumansCells
    63. Husson RN, Comeau AM, Hoff R. Diagnosis of human immunodeficiency virus infection in infants and children. Pediatrics. 1990 Jul; 86(1):1-10. PMID: 2193299.
      Citations: 13     Fields:    Translation:HumansCells
    64. Widmer G, Comeau AM, Furlong DB, Wirth DF, Patterson JL. Characterization of a RNA virus from the parasite Leishmania. Proc Natl Acad Sci U S A. 1989 Aug; 86(15):5979-82. PMID: 2762308.
      Citations: 44     Fields:    Translation:AnimalsCells
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