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Last Name
Institution

Gail Anne Pettit Bruns, Ph.D., M.D.

TitleAssociate Professor of Pediatrics
InstitutionChildren's Hospital Boston
DepartmentPediatrics
AddressChildrens Hospital
Pediatrics
300 Longwood Ave
Boston MA 02115
Phone617/355-7575
Fax617/355-7588

 Bibliographic 
 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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  1. Higgins AW, Alkuraya FS, Bosco AF, Brown KK, Bruns GA, Donovan DJ, Eisenman R, Fan Y, Farra CG, Ferguson HL, Gusella JF, Harris DJ, Herrick SR, Kelly C, Kim HG, Kishikawa S, Korf BR, Kulkarni S, Lally E, Leach NT, Lemyre E, Lewis J, Ligon AH, Lu W, Maas RL, MacDonald ME, Moore SD, Peters RE, Quade BJ, Quintero-Rivera F, Saadi I, Shen Y, Shendure J, Williamson RE, Morton CC. Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project. Am J Hum Genet. 2008 Mar; 82(3):712-22.
    View in: PubMed
  2. Kim HG, Higgins AW, Herrick SR, Kishikawa S, Nicholson L, Kutsche K, Ligon AH, Harris DJ, MacDonald ME, Bruns GA, Morton CC, Quade BJ, Gusella JF. Candidate loci for Zimmermann-Laband syndrome at 3p14.3. Am J Med Genet A. 2007 Jan 15; 143(2):107-11.
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  3. Kim HG, Herrick SR, Lemyre E, Kishikawa S, Salisz JA, Seminara S, MacDonald ME, Bruns GA, Morton CC, Quade BJ, Gusella JF. Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1. J Med Genet. 2005 Aug; 42(8):666-72.
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  4. Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, Fernandez BA, Kanematsu E, Gentles S, Christopoulos CC, Choufani S, Kwasnicka D, Zheng XH, Lai Z, Nusskern D, Zhang Q, Gu Z, Lu F, Zeesman S, Nowaczyk MJ, Teshima I, Chitayat D, Shuman C, Weksberg R, Zackai EH, Grebe TA, Cox SR, Kirkpatrick SJ, Rahman N, Friedman JM, Heng HH, Pelicci PG, Lo-Coco F, Belloni E, Shaffer LG, Pober B, Morton CC, Gusella JF, Bruns GA, Korf BR, Quade BJ, Ligon AH, Ferguson H, Higgins AW, Leach NT, Herrick SR, Lemyre E, Farra CG, Kim HG, Summers AM, Gripp KW, Roberts W, Szatmari P, Winsor EJ, Grzeschik KH, Teebi A, Minassian BA, Kere J, Armengol L, Pujana MA, Estivill X, Wilson MD, Koop BF, Tosi S, Moore GE, Boright AP, Zlotorynski E, Kerem B, Kroisel PM, Petek E, Oscier DG, Mould SJ, Döhner H, Döhner K, Rommens JM, Vincent JB, Venter JC, Li PW, Mural RJ, Adams MD, Tsui LC. Human chromosome 7: DNA sequence and biology. Science. 2003 May 2; 300(5620):767-72.
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  5. Sharon D, Bruns GA, McGee TL, Sandberg MA, Berson EL, Dryja TP. X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function. Invest Ophthalmol Vis Sci. 2000 Aug; 41(9):2712-21.
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  6. Vance JM, Matise TC, Wooster R, Schutte BC, Bruns GA, van Roy N, Brodeur GM, Tao YX, Gregory S, Weith A, Vaudin M, White P. Report and abstracts of the third international workshop on human chromosome 1 mapping 1997. Cytogenet Cell Genet. 1997; 78(3-4):154-82.
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  7. Fujita R, Bingham E, Forsythe P, McHenry C, Aita V, Navia BA, Dry K, Segal M, Devoto M, Bruns G, Wright AF, Ott J, Sieving PA, Swaroop A. A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3. Am J Hum Genet. 1996 Jul; 59(1):152-8.
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  8. White RA, Hughes RT, Adkison LR, Bruns G, Zon LI. The gene encoding protein kinase SEK1 maps to mouse chromosome 11 and human chromosome 17. Genomics. 1996 Jun 15; 34(3):430-2.
    View in: PubMed
  9. Molnár A, Wu P, Largespada DA, Vortkamp A, Scherer S, Copeland NG, Jenkins NA, Bruns G, Georgopoulos K. The Ikaros gene encodes a family of lymphocyte-restricted zinc finger DNA binding proteins, highly conserved in human and mouse. J Immunol. 1996 Jan 15; 156(2):585-92.
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  10. Weith A, Brodeur GM, Bruns GA, Matise TC, Mischke D, Nizetic D, Seldin MF, van Roy N, Vance J. Report of the second international workshop on human chromosome 1 mapping 1995. Cytogenet Cell Genet. 1996; 72(2-3):114-44.
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  11. Gawin B, Klamt B, König A, Thäte C, Le Paslier D, Chumakov I, Bhogal R, Zehetner G, Bruns G, Gessler M. An integrated YAC clone contig for the WAGR region on human chromosome 11p13-p14.1. Genomics. 1995 Nov 1; 30(1):37-45.
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  12. Krainc D, Haas M, Ward DC, Lipton SA, Bruns G, Leifer D. Assignment of human myocyte-specific enhancer binding factor 2C (hMEF2C) to human chromosome 5q14 and evidence that MEF2C is evolutionarily conserved. Genomics. 1995 Oct 10; 29(3):809-11.
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  13. Schwartz F, Eisenman R, Knoll J, Gessler M, Bruns G. cDNA sequence, genomic organization, and evolutionary conservation of a novel gene from the WAGR region. Genomics. 1995 Sep 20; 29(2):526-32.
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  14. Schwartz F, Neve R, Eisenman R, Gessler M, Bruns G. A WAGR region gene between PAX-6 and FSHB expressed in fetal brain. Hum Genet. 1994 Dec; 94(6):658-64.
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  15. Eichbaum Q, Clerc P, Bruns G, McKeon F, Ezekowitz RA. Assignment of the human macrophage mannose receptor gene (MRC1) to 10p13 by in situ hybridization and PCR-based somatic cell hybrid mapping. Genomics. 1994 Aug; 22(3):656-8.
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  16. Khurana TS, Engle EC, Bennett RR, Silverman GA, Selig S, Bruns GA, Kunkel LM. (CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein. Hum Mol Genet. 1994 May; 3(5):841.
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  17. Guay-Woodford LM, Bruns GA, D'Eustachio P. Identification of a simple sequence polymorphism within the mouse locus D12Nyu2. Mamm Genome. 1994 Apr; 5(4):251-2.
    View in: PubMed
  18. Dracopoli NC, Bruns GA, Brodeur GM, Landes GM, Matise TC, Seldin MF, Vance JM, Weith A. Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994. Cytogenet Cell Genet. 1994; 67(3):144-65.
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  19. Gorlin JB, Henske E, Warren ST, Kunst CB, D'Urso M, Palmieri G, Hartwig JH, Bruns G, Kwiatkowski DJ. Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28. Genomics. 1993 Aug; 17(2):496-8.
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  20. Gessler M, Bruns GA. Sequence of the WT1 upstream region including the Wit-1 gene. Genomics. 1993 Aug; 17(2):499-501.
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  21. Gessler M, König A, Moore J, Qualman S, Arden K, Cavenee W, Bruns G. Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome. Genes Chromosomes Cancer. 1993 Jul; 7(3):131-6.
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  22. Henry I, Hoovers J, Barichard F, Berthéas MF, Puech A, Prieur F, Gessler M, Bruns G, Mannens M, Junien C. Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family. Genes Chromosomes Cancer. 1993 May; 7(1):57-62.
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  23. Lia KM, Bruns GA, LeBeau MM, Silverman GA. pMCT108.2 is a chimaeric clone which physically maps to human chromosome bands 9q33 (D9S203) and 18q21.1 (D18S24). Hum Mol Genet. 1993 Mar; 2(3):332.
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  24. Silverman GA, Jenkins R, Bruns GA, LeBeau MM. Reassignment of pEFD70.3 (D18S23) to human chromosome band 21q22.2 (D21S412) by physical mapping. Hum Mol Genet. 1993 Mar; 2(3):331.
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  25. Brandt P, Ibrahim E, Bruns GA, Neve RL. Determination of the nucleotide sequence and chromosomal localization of the ATP2B2 gene encoding human Ca(2+)-pumping ATPase isoform PMCA2. Genomics. 1992 Oct; 14(2):484-7.
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  26. Bach I, Brunner HG, Beighton P, Ruvalcaba RH, Reardon W, Pembrey ME, van der Velde-Visser SD, Bruns GA, Cremers CW, Cremers FP, et al. Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3). Am J Hum Genet. 1992 Jul; 51(1):38-44.
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  27. Beggs AH, Byers TJ, Knoll JH, Boyce FM, Bruns GA, Kunkel LM. Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11. J Biol Chem. 1992 May 5; 267(13):9281-8.
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  28. Sims KB, Lebo RV, Benson G, Shalish C, Schuback D, Chen ZY, Bruns G, Craig IW, Golbus MS, Breakefield XO. The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3. Hum Mol Genet. 1992 May; 1(2):83-9.
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  29. Gessler M, König A, Bruns GA. The genomic organization and expression of the WT1 gene. Genomics. 1992 Apr; 12(4):807-13.
    View in: PubMed
  30. Dorfman DM, Wilson DB, Bruns GA, Orkin SH. Human transcription factor GATA-2. Evidence for regulation of preproendothelin-1 gene expression in endothelial cells. J Biol Chem. 1992 Jan 15; 267(2):1279-85.
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  31. Haase VH, Snijders AJ, Cooke SM, Teng MN, Kaul D, Le Beau MM, Bruns GA, Bernards A. Alternatively spliced ltk mRNA in neurons predicts a receptor with a larger putative extracellular domain. Oncogene. 1991 Dec; 6(12):2319-25.
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  32. Cotran PR, Bruns GA, Berson EL, Dryja TP. Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase. Exp Eye Res. 1991 Nov; 53(5):557-64.
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  33. Miwa T, Manabe Y, Kurokawa K, Kamada S, Kanda N, Bruns G, Ueyama H, Kakunaga T. Structure, chromosome location, and expression of the human smooth muscle (enteric type) gamma-actin gene: evolution of six human actin genes. Mol Cell Biol. 1991 Jun; 11(6):3296-306.
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  34. Collier IE, Bruns GA, Goldberg GI, Gerhard DS. On the structure and chromosome location of the 72- and 92-kDa human type IV collagenase genes. Genomics. 1991 Mar; 9(3):429-34.
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  35. Fontaine B, Khurana TS, Hoffman EP, Bruns GA, Haines JL, Trofatter JA, Hanson MP, Rich J, McFarlane H, Yasek DM, et al. Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene. Science. 1990 Nov 16; 250(4983):1000-2.
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  36. Dinauer MC, Pierce EA, Bruns GA, Curnutte JT, Orkin SH. Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease. J Clin Invest. 1990 Nov; 86(5):1729-37.
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  37. van Heyningen V, Bickmore WA, Seawright A, Fletcher JM, Maule J, Fekete G, Gessler M, Bruns GA, Huerre-Jeanpierre C, Junien C, et al. Role for the Wilms tumor gene in genital development? Proc Natl Acad Sci U S A. 1990 Jul; 87(14):5383-6.
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  38. Sankila EM, Bruns GA, Schwartz M, Nikoskelainen E, Niebuhr E, Hodgson SV, Wright AF, de la Chapelle A. DXS26 (HU16) is located in Xq21.1. Hum Genet. 1990 Jun; 85(1):117-20.
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  39. Ueyama H, Bruns G, Kanda N. Assignment of the vascular smooth muscle actin gene ACTSA to human chromosome 10. Jinrui Idengaku Zasshi. 1990 Jun; 35(2):145-50.
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  40. Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA. Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping. Nature. 1990 Feb 22; 343(6260):774-8.
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  41. Bruns GA, Dracopoli NC. Report of the committee on the genetic constitution of chromosome 1. Cytogenet Cell Genet. 1990; 55(1-4):77-85.
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  42. Zon LI, Tsai SF, Burgess S, Matsudaira P, Bruns GA, Orkin SH. The major human erythroid DNA-binding protein (GF-1): primary sequence and localization of the gene to the X chromosome. Proc Natl Acad Sci U S A. 1990 Jan; 87(2):668-72.
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  43. Sastry K, Herman GA, Day L, Deignan E, Bruns G, Morton CC, Ezekowitz RA. The human mannose-binding protein gene. Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10. J Exp Med. 1989 Oct 1; 170(4):1175-89.
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  44. Gessler M, Bruns GA. A physical map around the WAGR complex on the short arm of chromosome 11. Genomics. 1989 Jul; 5(1):43-55.
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  45. Gessler M, Simola KO, Bruns GA. Cloning of breakpoints of a chromosome translocation identifies the AN2 locus. Science. 1989 Jun 30; 244(4912):1575-8.
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  46. Gessler M, Thomas GH, Couillin P, Junien C, McGillivray BC, Hayden M, Jaschek G, Bruns GA. A deletion map of the WAGR region on chromosome 11. Am J Hum Genet. 1989 Apr; 44(4):486-95.
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  47. Shelley CS, Remold-O'Donnell E, Davis AE, Bruns GA, Rosen FS, Carroll MC, Whitehead AS. Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome. Proc Natl Acad Sci U S A. 1989 Apr; 86(8):2819-23.
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  48. Bruns GA, Sherman SL. Report of the committee on the genetic constitution of chromosome 1. Cytogenet Cell Genet. 1989; 51(1-4):67-90.
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  49. Sims KB, de la Chapelle A, Norio R, Sankila EM, Hsu YP, Rinehart WB, Corey TJ, Ozelius L, Powell JF, Bruns G, et al. Monoamine oxidase deficiency in males with an X chromosome deletion. Neuron. 1989 Jan; 2(1):1069-76.
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  50. Siddique T, McKinney R, Hung WY, Bartlett RJ, Bruns G, Mohandas TK, Ropers HH, Wilfert C, Roses AD. The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2. Genomics. 1988 Aug; 3(2):156-60.
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  51. Gessler M, Bruns GA. Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome. Genomics. 1988 Aug; 3(2):117-23.
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  52. Kwan SP, Sandkuyl LA, Blaese M, Kunkel LM, Bruns G, Parmley R, Skarshaug S, Page DC, Ott J, Rosen FS. Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. Genomics. 1988 Jul; 3(1):39-43.
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  53. Ozelius L, Hsu YP, Bruns G, Powell JF, Chen S, Weyler W, Utterback M, Zucker D, Haines J, Trofatter JA, et al. Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphism. Genomics. 1988 Jul; 3(1):53-8.
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  54. Stevens RL, Avraham S, Gartner MC, Bruns GA, Austen KF, Weis JH. Isolation and characterization of a cDNA that encodes the peptide core of the secretory granule proteoglycan of human promyelocytic leukemia HL-60 cells. J Biol Chem. 1988 May 25; 263(15):7287-91.
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  55. Kwiatkowski DJ, Bruns GA. Human profilin. Molecular cloning, sequence comparison, and chromosomal analysis. J Biol Chem. 1988 Apr 25; 263(12):5910-5.
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  56. Kosik KS, Orecchio LD, Bruns GA, Benowitz LI, MacDonald GP, Cox DR, Neve RL. Human GAP-43: its deduced amino acid sequence and chromosomal localization in mouse and human. Neuron. 1988 Apr; 1(2):127-32.
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  57. Kwiatkowski DJ, Westbrook CA, Bruns GA, Morton CC. Localization of gelsolin proximal to ABL on chromosome 9. Am J Hum Genet. 1988 Apr; 42(4):565-72.
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  58. Matsuoka R, Chambers A, Kimura M, Kanda N, Bruns G, Yoshida M, Takao A. Molecular cloning and chromosomal localization of a gene coding for human cardiac myosin heavy-chain. Am J Med Genet. 1988 Feb; 29(2):369-76.
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  59. Sherman SL, Bruns GA. Report of the committee on the genetic constitution of chromosome 1. Cytogenet Cell Genet. 1988; 49(1-3):39-45.
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  60. Arbiser JL, Morton CC, Bruns GA, Majzoub JA. Human corticotropin releasing hormone gene is located on the long arm of chromosome 8. Cytogenet Cell Genet. 1988; 47(3):113-6.
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  61. Kiyama R, Okumura K, Matsui H, Bruns GA, Kanda N, Oishi M. Nature of recombination involved in excision and rearrangement of human repetitive DNA. J Mol Biol. 1987 Dec 20; 198(4):589-98.
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  62. Harris P, Lalande M, Stroh H, Bruns G, Flint A, Latt SA. Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p. Hum Genet. 1987 Oct; 77(2):95-103.
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  63. Goldberger G, Bruns GA, Rits M, Edge MD, Kwiatkowski DJ. Human complement factor I: analysis of cDNA-derived primary structure and assignment of its gene to chromosome 4. J Biol Chem. 1987 Jul 25; 262(21):10065-71.
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  64. Ramesh V, Eddy R, Bruns GA, Shih VE, Shows TB, Gusella JF. Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes. Hum Genet. 1987 Jun; 76(2):121-6.
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  65. Stewart GD, Bruns GA, Wasmuth JJ, Kurnit DM. An anonymous DNA segment (II227) maps to the long arm of human chromosome 5 and identifies a BstXI polymorphism (D5S26). Nucleic Acids Res. 1987 May 11; 15(9):3939.
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  66. Bruns G, Stroh H, Veldman GM, Latt SA, Floros J. The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10. Hum Genet. 1987 May; 76(1):58-62.
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  67. Bartlett RJ, Pericak-Vance MA, Yamaoka L, Gilbert J, Herbstreith M, Hung WY, Lee JE, Mohandas T, Bruns G, Laberge C, et al. A new probe for the diagnosis of myotonic muscular dystrophy. Science. 1987 Mar 27; 235(4796):1648-50.
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  68. Gold DP, van Dongen JJ, Morton CC, Bruns GA, van den Elsen P, Geurts van Kessel AH, Terhorst C. The gene encoding the epsilon subunit of the T3/T-cell receptor complex maps to chromosome 11 in humans and to chromosome 9 in mice. Proc Natl Acad Sci U S A. 1987 Mar; 84(6):1664-8.
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  69. Tanzi RE, Gusella JF, Watkins PC, Bruns GA, St George-Hyslop P, Van Keuren ML, Patterson D, Pagan S, Kurnit DM, Neve RL. Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus. Science. 1987 Feb 20; 235(4791):880-4.
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  70. Van Keuren ML, Hart IM, Kao FT, Neve RL, Bruns GA, Kurnit DM, Patterson D. A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity. Cytogenet Cell Genet. 1987; 44(2-3):142-7.
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  71. Morton NE, Bruns GA. Report of the committee on the genetic-constitution of chromosomes 1 and 2. Cytogenet Cell Genet. 1987; 46(1-4):102-30.
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  72. Weis JH, Morton CC, Bruns GA, Weis JJ, Klickstein LB, Wong WW, Fearon DT. A complement receptor locus: genes encoding C3b/C4b receptor and C3d/Epstein-Barr virus receptor map to 1q32. J Immunol. 1987 Jan 1; 138(1):312-5.
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  73. Yang-Feng TL, Bruns GA, Carroll AJ, Simola KO, Francke U. Localization of the LDHA gene to 11p14----11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13. Hum Genet. 1986 Dec; 74(4):331-4.
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  74. Litt M, Sheehy R, Bruns GA, Magenis RE. A polymorphic locus on the long arm of chromosome 20 defined by two probes from a single cosmid. Hum Genet. 1986 Aug; 73(4):340-5.
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  75. Donlon TA, Lalande M, Wyman A, Bruns G, Latt SA. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. Proc Natl Acad Sci U S A. 1986 Jun; 83(12):4408-12.
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  76. Glaser T, Lewis WH, Bruns GA, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KO, et al. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus. Nature. 1986 Jun 26-Jul 2; 321(6073):882-7.
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  77. Shiloh Y, Donlon T, Bruns G, Breitman ML, Tsui LC. Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36. Hum Genet. 1986 May; 73(1):17-9.
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  78. Davis AE, Whitehead AS, Harrison RA, Dauphinais A, Bruns GA, Cicardi M, Rosen FS. Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11. Proc Natl Acad Sci U S A. 1986 May; 83(10):3161-5.
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  79. Bufton L, Bruns GA, Magenis RE, Tomar D, Shaw D, Brook D, Litt M. Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19. Am J Hum Genet. 1986 Apr; 38(4):447-60.
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  80. Litt M, Bruns GA, Sheehy R, Magenis RE. A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37. Am J Hum Genet. 1986 Mar; 38(3):288-96.
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  81. Huang LS, Miller DA, Bruns GA, Breslow JL. Mapping of the human APOB gene to chromosome 2p and demonstration of a two-allele restriction fragment length polymorphism. Proc Natl Acad Sci U S A. 1986 Feb; 83(3):644-8.
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  82. Kwan SP, Kunkel L, Bruns G, Wedgwood RJ, Latt S, Rosen FS. Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism. J Clin Invest. 1986 Feb; 77(2):649-52.
    View in: PubMed
  83. Latt SA, Shiloh Y, Sakai K, Brodeur G, Donlon T, Korf B, Shipley J, Bruns G, Heartlein M, Kanda N, et al. Novel DNA rearrangement phenomena associated with DNA amplification in human neuroblastomas and neuroblastoma cell lines. Prog Clin Biol Res. 1986; 209A:601-12.
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  84. Housman DE, Glaser T, Gerhard DS, Jones C, Bruns GA, Lewis WH. Mapping of human chromosome 11: organization of genes within the Wilms' tumor region of the chromosome. Cold Spring Harb Symp Quant Biol. 1986; 51 Pt 2:837-41.
    View in: PubMed
  85. Ma NS, Gerhard DS, Housman DE, Orkin S, Bruns G. Owl monkey gene mapping: the assignment of gene loci for catalase, beta-globin gene cluster, HRAS1, insulin, and parathyroid hormone. Cytogenet Cell Genet. 1986; 43(1-2):57-68.
    View in: PubMed
  86. Buroker NE, Magenis RE, Weliky K, Bruns G, Litt M. Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q. Hum Genet. 1986 Jan; 72(1):86-94.
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  87. Kurnit DM, Roy S, Stewart GD, Schwedock J, Neve RL, Bruns GA, Van Keuren ML, Patterson D. The 724 family of DNA sequences is interspersed about the pericentromeric regions of human acrocentric chromosomes. Cytogenet Cell Genet. 1986; 43(1-2):109-16.
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  88. Jackson CL, Bruns GA, Breslow JL. Isolation of cDNA and genomic clones for apolipoprotein C-II. Methods Enzymol. 1986; 128:788-800.
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  89. Yamaoka LH, Bartlett RJ, Ross DA, Fey GH, Ledbetter DH, Bruns G, Pericak-Vance MA, Herbstreith MH, Roses AD. Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy. J Neurogenet. 1985 Dec; 2(6):403-12.
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  90. Benchimol S, Lamb P, Crawford LV, Sheer D, Shows TB, Bruns GA, Peacock J. Transformation associated p53 protein is encoded by a gene on human chromosome 17. Somat Cell Mol Genet. 1985 Sep; 11(5):505-10.
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  91. Mukai S, Dryja TP, Bruns GA, Aldridge JF, Berson EL. Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locus. Am J Ophthalmol. 1985 Aug 15; 100(2):225-9.
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  92. Shiloh Y, Kanda N, Kunkel LM, Bruns G, Sakai K, Latt SA. Two RFLPs identified by a human chromosome #2 clone at 2p15-2p16 (HGM8 assignment no. D2S5). Nucleic Acids Res. 1985 Jul 25; 13(14):5403.
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  93. Mantzouranis EC, Dowton SB, Whitehead AS, Edge MD, Bruns GA, Colten HR. Human serum amyloid P component. cDNA isolation, complete sequence of pre-serum amyloid P component, and localization of the gene to chromosome 1. J Biol Chem. 1985 Jun 25; 260(12):7752-6.
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  94. Ginsburg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA, Orkin SH. Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. Science. 1985 Jun 21; 228(4706):1401-6.
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  95. Michelson AM, Bruns GA, Morton CC, Orkin SH. The human phosphoglycerate kinase multigene family. HLA-associated sequences and an X-linked locus containing a processed pseudogene and its functional counterpart. J Biol Chem. 1985 Jun 10; 260(11):6982-92.
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  96. Shiloh Y, Shipley J, Brodeur GM, Bruns G, Korf B, Donlon T, Schreck RR, Seeger R, Sakai K, Latt SA. Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines. Proc Natl Acad Sci U S A. 1985 Jun; 82(11):3761-5.
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  97. Das HK, McPherson J, Bruns GA, Karathanasis SK, Breslow JL. Isolation, characterization, and mapping to chromosome 19 of the human apolipoprotein E gene. J Biol Chem. 1985 May 25; 260(10):6240-7.
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  98. Caccia N, Bruns GA, Kirsch IR, Hollis GF, Bertness V, Mak TW. T cell receptor alpha chain genes are located on chromosome 14 at 14q11-14q12 in humans. J Exp Med. 1985 May 1; 161(5):1255-60.
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  99. van den Elsen P, Bruns G, Gerhard DS, Pravtcheva D, Jones C, Housman D, Ruddle FA, Orkin S, Terhorst C. Assignment of the gene coding for the T3-delta subunit of the T3-T-cell receptor complex to the long arm of human chromosome 11 and to mouse chromosome 9. Proc Natl Acad Sci U S A. 1985 May; 82(9):2920-4.
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  100. de Martinville B, Kunkel LM, Bruns G, Morlé F, Koenig M, Mandel JL, Horwich A, Latt SA, Gusella JF, Housman D, et al. Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus. Am J Hum Genet. 1985 Mar; 37(2):235-49.
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  101. Bruns G, Kavathas P, Shiloh Y, Sakai K, Schwaber J, Latt SA, Herzenberg LA. The human T cell antigen Leu-2 (T8) is encoded on chromosome 2. Hum Genet. 1985; 70(4):311-4.
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  102. Whitehead AS, Skinner M, Bruns GA, Costello W, Edge MD, Cohen AS, Sipe JD. Cloning of human prealbumin complementary DNA. Localization of the gene to chromosome 18 and detection of a variant prealbumin allele in a family with familial amyloid polyneuropathy. Mol Biol Med. 1984 Dec; 2(6):411-23.
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  103. Caccia N, Kronenberg M, Saxe D, Haars R, Bruns GA, Goverman J, Malissen M, Willard H, Yoshikai Y, Simon M, et al. The T cell receptor beta chain genes are located on chromosome 6 in mice and chromosome 7 in humans. Cell. 1984 Jul; 37(3):1091-9.
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  104. Aldridge J, Kunkel L, Bruns G, Tantravahi U, Lalande M, Brewster T, Moreau E, Wilson M, Bromley W, Roderick T, et al. A strategy to reveal high-frequency RFLPs along the human X chromosome. Am J Hum Genet. 1984 May; 36(3):546-64.
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  105. Jackson CL, Bruns GA, Breslow JL. Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII. Proc Natl Acad Sci U S A. 1984 May; 81(10):2945-9.
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  106. Dryja TP, Cavenee W, White R, Rapaport JM, Petersen R, Albert DM, Bruns GA. Homozygosity of chromosome 13 in retinoblastoma. N Engl J Med. 1984 Mar 1; 310(9):550-3.
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  107. Bruns GA, Karathanasis SK, Breslow JL. Human apolipoprotein A-I--C-III gene complex is located on chromosome 11. Arteriosclerosis. 1984 Mar-Apr; 4(2):97-102.
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  108. Brook JD, Shaw DJ, Meredith L, Bruns GA, Harper PS. Localisation of genetic markers and orientation of the linkage group on chromosome 19. Hum Genet. 1984; 68(4):282-5.
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  109. Dryja TP, Rapaport JM, Weichselbaum R, Bruns GA. Chromosome 13 restriction fragment length polymorphisms. Hum Genet. 1984; 65(4):320-4.
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  110. Kurnit DM, Neve RL, Morton CC, Bruns GA, Ma NS, Cox DR, Klinger HP. Recent evolution of DNA sequence homology in the pericentromeric regions of human acrocentric chromosomes. Cytogenet Cell Genet. 1984; 38(2):99-105.
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  111. Kohl NE, Kanda N, Schreck RR, Bruns G, Latt SA, Gilbert F, Alt FW. Transposition and amplification of oncogene-related sequences in human neuroblastomas. Cell. 1983 Dec; 35(2 Pt 1):359-67.
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  112. Orkin SH, Daddona PE, Shewach DS, Markham AF, Bruns GA, Goff SC, Kelley WN. Molecular cloning of human adenosine deaminase gene sequences. J Biol Chem. 1983 Nov 10; 258(21):12753-6.
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  113. Neve RL, Bruns GA, Dryja TP, Kurnit DM. Retrieval of human DNA from rodent-human genomic libraries by a recombination process. Gene. 1983 Sep; 23(3):343-54.
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  114. Kanda N, Schreck R, Alt F, Bruns G, Baltimore D, Latt S. Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes. Proc Natl Acad Sci U S A. 1983 Jul; 80(13):4069-73.
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  115. Whitehead AS, Bruns GA, Markham AF, Colten HR, Woods DE. Isolation of human C-reactive protein complementary DNA and localization of the gene to chromosome 1. Science. 1983 Jul 1; 221(4605):69-71.
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  116. Dryja TP, Bruns GA, Gallie B, Petersen R, Green W, Rapaport JM, Albert DM, Gerald PS. Low incidence of deletion of the esterase D locus in retinoblastoma patients. Hum Genet. 1983; 64(2):151-5.
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  117. Bruns G. [Prognosis in tumor diagnosis]. Arch Geschwulstforsch. 1983; 53(5):497-506.
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  118. Dryja TP, Bruns GA, Orkin SH, Albert DM, Gerald PS. Isolation of DNA fragments from chromosome 13. Retina. 1983; 3(2):121-5.
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  119. Gerald PS, Bruns GA. Recombinant DNA and the analysis of cytogenetic disorders associated with mental retardation. Res Publ Assoc Res Nerv Ment Dis. 1983; 60:173-9.
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  120. Kurnit DM, Philipp BW, Bruns GA. Confirmation of the mapping assignment of human serum albumin to chromosome 4 using a cloned human albumin gene. Cytogenet Cell Genet. 1982; 34(4):282-8.
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  121. Bruns GA, Mintz BJ, Leary AC, Regina VM, Gerald PS. Human lysosomal genes: arylsulfatase A and beta-galactosidase. Biochem Genet. 1979 Dec; 17(11-12):1031-59.
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  122. Minna JD, Bruns GA, Krinsky AH, Lalley PA, Francke U, Gerald PS. Assignment of a Mus musculus gene for triosephosphate isomerase to chromosome 6 and for glyoxalase-I to chromosome 17 using somatic cell hybrids. Somatic Cell Genet. 1978 Mar; 4(2):241-52.
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  123. Bruns GA, Leary AC, Eisenman RE, Bazinet CW, Regina VM, Gerald PS. Expression of ACONS and GALT in man-rodent somatic cell hybrids. Cytogenet Cell Genet. 1978; 22(1-6):172-6.
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  124. Gerald PS, Bruns GA. Genetic determinants of viral susceptibility. Birth Defects Orig Artic Ser. 1978; 14(6A):1-7.
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  125. Bruns GA, Mintz BJ, Leary AC, Regina VM, Gerald PS. Expression of human arylsulfatase-A in man-hamster somatic cell hybrids. Cytogenet Cell Genet. 1978; 22(1-6):182-5.
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  126. Rahmann H, Bruns GA. Production on nonserogenous CSF compounds in the CNS of teleosts. Adv Neurol. 1978; 20:103-9.
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  127. Bruns GA, Pierce P, Regina VM, Gerald PS. Expression of GAPDH and TPI in dog-rodent hybrids. Cytogenet Cell Genet. 1978; 22(1-6):547-51.
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  128. Bruns GA, Leary AC, Regina VM, Gerald PS. Lysosomal beta-D-galactosidase in man-hamster somatic cell hybrids. Cytogenet Cell Genet. 1978; 22(1-6):177-81.
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  129. Bruns GA, Regina VM. Adenylate kinase 2, a mitochondrial enzyme. Biochem Genet. 1977 Jun; 15(5-6):477-86.
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  130. Ingram PH, Bruns GA, Regina VM, Eisenman RE, Gerald PS. Expression of alpha-D-mannosidase in man-hamster somatic cell hybrids. Biochem Genet. 1977 Jun; 15(5-6):455-76.
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  131. Bruns GA. Complement genes on chromosome 6. N Engl J Med. 1977 Mar 3; 296(9):510-11.
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  132. Benn P, Chern CJ, Bruns G, Craig IW, Croce CM. Assignment of the genes for human beta-glucuronidase and mitochondrial malate dehydrogenase to the region pter leads to q22 of chromosome 7. Cytogenet Cell Genet. 1977; 19(5):273-80.
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  133. Bruns GA, Gerald PS. Human glyceraldehyde-3-phosphate dehydrogenase in man-rodent somatic cell hybrids. Science. 1976 Apr 2; 192(4234):54-6.
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  134. Bruns GA, Gerald PS. Expression of the human adenylate kinase isozymes, phosphopyruvate hydratase, 6-phosphogluconate dehydrogenase, and phosphoglucomutase-1 in man-rodent somatic cell hybrids. Biochem Genet. 1976 Feb; 14(1-2):1-17.
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  135. Bruns GA, Eisenman RE, Gerald PS. Human mitochondrial NADP-dependent isocitrate dehydrogenase in man-mouse somatic cell hybrids. Cytogenet Cell Genet. 1976; 17(4):200-11.
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  136. Bruns GA, Gerald PS. Human acid phosphatase in somatic cell hybrids. Science. 1974 Apr 26; 184(4135):480-2.
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  137. Bruns G, Gerald PS. Proceedings: The syntenic relationship of the genes for human lysosomal acid phosphatase, isozyme C, and LDH-A. Cytogenet Cell Genet. 1974; 13(1):69-72.
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  138. Bruns GA, Ingram VM. The erythroid cells and haemoglobins of the chick embryo. Philos Trans R Soc Lond B Biol Sci. 1973 Oct 25; 266(877):225-305.
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  139. Bruns GA, Ingram VM. Progenitor cells of the definitive erythroid series in the chick embryo. Dev Biol. 1973 Mar; 31(1):192-4.
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  140. Bruns GA, Ingram VM. Erythropoiesis in the developing chick embryo. Dev Biol. 1973 Feb; 30(2):455-9.
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