Raju Kucherlapati headshot

Raju Kucherlapati, Ph.D.

Paul C. Cabot Professor of Genetics, Harvard Medical School
617-525-4445
Kucherlapati Lab Website
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia.
Authors: Authors: Lencz T, Morgan TV, Athanasiou M, Dain B, Reed CR, Kane JM, Kucherlapati R, Malhotra AK.
Mol Psychiatry
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Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia.
Authors: Authors: Kratz CP, Niemeyer CM, Thomas C, Bauhuber S, Matejas V, Bergsträsser E, Flotho C, Flores NJ, Haas O, Hasle H, van den Heuvel-Eibrink MM, Kucherlapati RS, Lang P, Roberts AE, Starý J, Strahm B, Swanson KD, Trebo M, Zecca M, Neel B, Locatelli F, Loh ML, Zenker M.
Leukemia
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Raju Kucherlapati talks about personalised medicine: breathing new life into old drugs. Interview by Steve Carney.
Authors: Authors: Kucherlapati R.
Drug Discov Today
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Analysis of TBX1 variation in patients with psychotic and affective disorders.
Authors: Authors: Funke BH, Lencz T, Finn CT, DeRosse P, Poznik GD, Plocik AM, Kane J, Rogus J, Malhotra AK, Kucherlapati R.
Mol Med
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Response to treatment and survival of patients with non-small cell lung cancer undergoing somatic EGFR mutation testing.
Authors: Authors: Sequist LV, Joshi VA, Jänne PA, Muzikansky A, Fidias P, Meyerson M, Haber DA, Kucherlapati R, Johnson BE, Lynch TJ.
Oncologist
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Germline gain-of-function mutations in SOS1 cause Noonan syndrome.
Authors: Authors: Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS.
Nat Genet
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DTNBP1 genotype influences cognitive decline in schizophrenia.
Authors: Authors: Burdick KE, Goldberg TE, Funke B, Bates JA, Lencz T, Kucherlapati R, Malhotra AK.
Schizophr Res
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A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions.
Authors: Authors: Funke BH, Brown AC, Ramoni MF, Regan ME, Baglieri C, Finn CT, Babcock M, Shprintzen RJ, Morrow BE, Kucherlapati R.
Genet Test
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Participation of mouse DNA polymerase iota in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer.
Authors: Authors: Dumstorf CA, Clark AB, Lin Q, Kissling GE, Yuan T, Kucherlapati R, McGregor WG, Kunkel TA.
Proc Natl Acad Sci U S A
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Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome.
Authors: Authors: Long JM, LaPorte P, Merscher S, Funke B, Saint-Jore B, Puech A, Kucherlapati R, Morrow BE, Skoultchi AI, Wynshaw-Boris A.
Neurogenetics
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