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10 Article(s) on File
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Tackling antibiotic resistance
Bush K,
Courvalin P,
Dantas G,
Davies J,
Eisenstein B,
Huovinen P,
Jacoby GA,
Kishony R,
Kreiswirth BN,
Kutter E,
Lerner SA,
Levy S,
Lewis K,
Lomovskaya O,
Miller JH,
Mobashery S,
Piddock LJ,
Projan S,
Thomas CM,
Tomasz A,
Tulkens PM,
Walsh TR,
Watson JD,
Witkowski J,
Witte W,
Wright G,
Yeh P,
Zgurskaya HI

Nature Reviews Microbiology
  9 (12): 894-896; Dec 2011  
[Abstract]
[DOI] [Full Text]

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
Nord AS,
Roeb W,
Dickel DE,
Walsh T,
Kusenda M,
OConnor KL,
Malhotra D,
McCarthy SE,
Stray SM,
Taylor SM,
Sebat J,
King B,
King MC,
McClellan JM

European Journal of Human Genetics
  19 (6): 727-731; Jun 2011   Elsevier PMC3110052
[Abstract]
[DOI]

Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51
Walsh T,
Pierce SB,
Lenz DR,
Brownstein Z,
Dagan-Rosenfeld O,
Shahin H,
Roeb W,
McCarthy SE,
Nord AS,
Gordon CR,
Ben-Neriah Z,
Sebat J,
Kanaan M,
Lee MK,
Frydman M,
King MC,
Avraham KB

American Journal of Human Genetics
  87 (1): 101-109 ; Jul 9 2010   PMCID: PMC2896780
[Abstract]
[DOI] [Full Text] [PDF]

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Girirajan S,
Rosenfeld JA,
Cooper GM,
Antonacci F,
Siswara P,
Itsara A,
Vives L,
Walsh T,
McCarthy SE,
Baker C,
Mefford HC,
Kidd JM,
Browning SR,
Browning BL,
Dickel DE,
Levy DL,
Ballif BC,
Platky K,
Farber DM,
Gowans GC,
Wetherbee JJ,
Asamoah A,
Weaver DD,
Mark PR,
Dickerson J,
Garg BP,
Ellingwood SA,
Smith R,
Banks VC,
Smith W,
McDonald MT,
Hoo JJ,
French BN,
Hudson C,
Johnson JP,
Ozmore JR,
Moeschler JB,
Surti U,
Escobar LF,
El-Khechen D,
Gorski JL,
Kussmann J,
Salbert B,
Lacassie Y,
Biser A,
McDonald-McGinn DM,
Zackai EH,
Deardorff MA,
Shaikh TH,
Haan E,
Friend KL,
Fichera M,
Romano C,
Gécz J,
DeLisi LE,
Sebat J,
King MC,
Shaffer LG,
Eichler EE

Nature Genetics
  (0): Feb 14 2010   PMCID: PMC2847896
[Abstract]
[DOI] [Full Text] [PDF]

Microduplications of 16p11.2 are associated with schizophrenia
McCarthy SE,
Makarov V,
Kirov G,
Addington AM,
McClellan J,
Yoon S,
Perkins DO,
Dickel DE,
Kusenda M,
Krastoshevsky O,
Krause V,
Kumar RA,
Grozeva D,
Malhotra D,
Walsh T,
Zackai EH,
Kaplan P,
Ganesh J,
Krantz ID,
Spinner NB,
Roccanova P,
Bhandari A,
Pavon K,
Lakshmi B,
Leotta A,
Kendall JT,
Lee YH,
Vacic V,
Gary S,
Iakoucheva LM,
Crow TJ,
Christian SL,
Lieberman JA,
Stroup TS,
Lehtimaki T,
Puura K,
Haldeman-Englert C,
Pearl J,
Goodell M,
Willour VL,
DeRosse P,
Steele J,
Kassem L,
Wolff J,
Chitkara N,
McMahon FJ,
Malhotra AK,
Potash JB,
Schulze TG,
Nothen MM,
Cichon S,
Rietschel M,
Leibenluft E,
Kustanovich V,
Lajonchere CM,
Sutcliffe JS,
Skuse D,
Gill M,
Gallagher L,
Mendell NR,
Craddock N,
Owen MJ,
ODonovan MC,
Shaikh TH,
Susser E,
DeLisi LE,
Sullivan PF,
Deutsch CK,
Rapoport J,
Levy DL,
King MC,
Sebat J

Nature Genetics
  41 (11): 1223-1227; Nov 2009   PMCID: PMC2951180
[Abstract]
[DOI] [Full Text] [PDF]

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
Mefford HC,
Sharp AJ,
Baker C,
Itsara A,
Jiang Z,
Buysse K,
Huang S,
Maloney VK,
Crolla JA,
Baralle D,
Collins A,
Mercer C,
Norga K,
de Ravel T,
Devriendt K,
Bongers EM,
de Leeuw N,
Reardon W,
Gimelli S,
Bena F,
Hennekam RC,
Male A,
Gaunt L,
Clayton-Smith J,
Simonic I,
Park SM,
Mehta SG,
Nik-Zainal S,
Woods CG,
Firth HV,
Parkin G,
Fichera M,
Reitano S,
Lo Giudice M,
Li KE,
Casuga I,
Broomer A,
Conrad B,
Schwerzmann M,
Raber L,
Gallati S,
Striano P,
Coppola A,
Tolmie JL,
Tobias ES,
Lilley C,
Armengol L,
Spysschaert Y,
Verloo P,
De Coene A,
Goossens L,
Mortier G,
Speleman F,
van Binsbergen E,
Nelen MR,
Hochstenbach R,
Poot M,
Gallagher L,
Gill M,
McClellan J,
King MC,
Regan R,
Skinner C,
Stevenson RE,
Antonarakis SE,
Chen C,
Estivill X,
Menten B,
Gimelli G,
Gribble S,
Schwartz S,
Sutcliffe JS,
Walsh T,
Knight SJ,
Sebat J,
Romano C,
Schwartz CE,
Veltman JA,
de Vries BB,
Vermeesch JR,
Barber JC,
Willatt L,
Tassabehji M,
Eichler EE

N Engl J Med
  359 (16): 1685-99; Oct 16 2008   PMCID: PMC2703742
[Abstract]
[DOI] [Full Text] [PDF]

Gene mutations and cognitive delay - Response
McClellan JM,
Walsh T,
McCarthy SE,
King MC,
Sebat J

Science
  321 (5889): 640-640; Aug 1 2008  
[DOI] [Full Text] [PDF]

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Walsh T,
McClellan JM,
McCarthy SE,
Addington AM,
Pierce SB,
Cooper GM,
Nord AS,
Kusenda M,
Malhotra D,
Bhandari A,
Stray SM,
Rippey CF,
Roccanova P,
Makarov V,
Lakshmi B,
Findling RL,
Sikich L,
Stromberg T,
Merriman B,
Gogtay N,
Butler P,
Eckstrand K,
Noory L,
Gochman P,
Long R,
Chen Z,
Davis S,
Baker C,
Eichler EE,
Meltzer PS,
Nelson SF,
Singleton AB,
Lee MK,
Rapoport JL,
King MC,
Sebat J

Science
  320 (5875): 539-43; Apr 25 2008  
[Abstract]
[DOI] [Full Text] [PDF]

Strong Association of De Novo Copy Number Mutations with Autism
Sebat J,
Lakshmi B,
Malhotra D,
Troge JE,
Lese-Martin C,
Walsh T,
Yamrom B,
Yoon S,
Krasnitz A,
Kendall JT,
Leotta A,
Pai D,
Zhang R,
Lee YH,
Hicks JB,
Spence SJ,
Lee AT,
Puura K,
Lehtimaki T,
Ledbetter D,
Gregersen PK,
Bregman J,
Sutcliffe JS,
Jobanputra V,
Chung W,
Warburton D,
King MC,
Skuse D,
Geschwind DH,
Gilliam TC,
Ye K,
Wigler MH

Science
  316 (5823): 445-449; April 20 2007  
[Abstract]
[DOI] [Full Text] [PDF]

DBC2, a candidate for a tumor suppressor gene involved in breast cancer
Hamaguchi M,
Meth JL,
von Klitzing C,
Wei W,
Esposito D,
Rodgers L,
Walsh T,
Welcsh P,
King MC,
Wigler MH

Proceedings of the National Academy of Sciences of the United States of America
  99 (21): 13647-13652; Oct 2002  
[Full Text]


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