Louis Martens Kunkel

Louis Martens Kunkel, Ph.D.

Professor of Genetics and Pediatrics, Harvard Medical School

Director, Genomics Program

617-355-7576

Kunkel Lab Website

Publications

Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome.

Authors: Authors: Sirotkin H, O'Donnell H, DasGupta R, Halford S, St Jore B, Puech A, Parimoo S, Morrow B, Skoultchi A, Weissman SM, Scambler P, Kucherlapati R.
Genomics 1997-04-01
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A mouse model of human familial adenomatous polyposis.

Authors: Authors: Yang K, Edelmann W, Fan K, Lau K, Kolli VR, Fodde R, Khan PM, Kucherlapati R, Lipkin M.
J Exp Zool 1997-02-15
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Loss of Apc and the entire chromosome 18 but absence of mutations at the Ras and Tp53 genes in intestinal tumors from Apc1638N, a mouse model for Apc-driven carcinogenesis.

Authors: Authors: Smits R, Kartheuser A, Jagmohan-Changur S, Leblanc V, Breukel C, de Vries A, van Kranen H, van Krieken JH, Williamson S, Edelmann W, Kucherlapati R, Fodde R.
Carcinogenesis 1997-02-01
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AICL: a new activation-induced antigen encoded by the human NK gene complex.

Authors: Authors: Hamann J, Montgomery KT, Lau S, Kucherlapati R, van Lier RA.
Immunogenetics 1997-01-01
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Report of the fourth International Workshop in Human Chromosome 12 Mapping, 1997.

Authors: Authors: Kucherlapati R, Marynen P, Turc-Carel C.
Cytogenet Cell Genet 1997-01-01
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Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

Authors: Authors: Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE.
Nat Genet 1997-01-01
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Characterization of human DSPG3, a small dermatan sulfate proteoglycan.

Authors: Authors: Deere M, Johnson J, Garza S, Harrison WR, Yoon SJ, Elder FF, Kucherlapati R, Hook M, Hecht JT.
Genomics 1996-12-15
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Physical mapping of the human neurotensin gene (NTS) between markers D12S1444 and D12S81 on chromosome 12q21.

Authors: Authors: Marondel I, Renault B, Lieman J, Ward D, Kucherlapati R.
Genomics 1996-12-01
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Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

Authors: Authors: Papolos DF, Faedda GL, Veit S, Goldberg R, Morrow B, Kucherlapati R, Shprintzen RJ.
Am J Psychiatry 1996-12-01
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Linkage of asthma and total serum IgE concentration to markers on chromosome 12q: evidence from Afro-Caribbean and Caucasian populations.

Authors: Authors: Barnes KC, Neely JD, Duffy DL, Freidhoff LR, Breazeale DR, Schou C, Naidu RP, Levett PN, Renault B, Kucherlapati R, Iozzino S, Ehrlich E, Beaty TH, Marsh DG.
Genomics 1996-10-01
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