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14 Article(s) on File
Page 1 of 1
The contribution of de novo coding mutations to autism spectrum disorder
Iossifov I,
ORoak BJ,
Sanders SJ,
Ronemus M,
Krumm N,
Levy D,
Stessman HA,
Witherspoon KT,
Vives L,
Patterson KE,
Smith JD,
Paeper B,
Nickerson DA,
Dea J,
Dong S,
Gonzalez LE,
Mandell JD,
Mane SM,
Murtha MT,
Sullivan CA,
Walker MF,
Waqar Z,
Wei L,
Willsey AJ,
Yamrom B,
Lee YH,
Grabowska E,
Dalkic E,
Wang Z,
Marks S,
Andrews P,
Leotta A,
Kendall J,
Hakker I,
Rosenbaum J,
Ma B,
Rodgers L,
Troge J,
Narzisi G,
Yoon S,
Schatz MC,
Ye K,
McCombie WR,
Shendure J,
Eichler EE,
State MW,
Wigler M

Nature
  515 (7526): 2160-U136; Nov 13 2014   NLM
[Abstract]
[DOI] [Full Text]

Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data
Glessner JT,
Bick AG,
Ito K,
Homsy JG,
Rodriguez-Murillo L,
Fromer M,
Mazaika E,
Vardarajan B,
Italia M,
Leipzig J,
DePalma SR,
Golhar R,
Sanders SJ,
Yamrom B,
Ronemus M,
Iossifov I,
Willsey AJ,
State MW,
Kaltman JR,
White PS,
Shen Y,
Warburton D,
Brueckner M,
Seidman C,
Goldmuntz E,
Gelb BD,
Lifton R,
Seidman J,
Hakonarson H,
Chung WK

Circulation Research
  115 (10): 884-96; Oct 24 2014   Nlm
[Abstract]
[DOI] [Full Text]

Accurate de novo and transmitted indel detection in exome-capture data using microassembly
Narzisi G,
ORawe JA,
Iossifov I,
Fang H,
Lee Yh,
Wang Z,
Wu Y,
Lyon GJ,
Wigler M,
Schatz MC

Nature Methods
  11 (10): 1033-1036; Oct 2014   NLM
[Abstract]
[DOI] [Full Text]

Target-independent prediction of drug synergies using only drug lipophilicity
Yilancioglu K,
Weinstein ZB,
Meydan C,
Akhmetov A,
Toprak I,
Durmaz A,
Iossifov I,
Kazan H,
Roth FP,
Cokol M

Journal of Chemical Information and Modeling
  54 (8): 2286-2293; Aug 25 2014   NLM
[Abstract]
[DOI] [Full Text]

Large-Scale Identification and Analysis of Suppressive Drug Interactions
Cokol M,
Weinstein Z,
Yilancioglu K,
Tasan M,
Doak A,
Cansever D,
Mutlu B,
Li S,
Rodriguez-Esteban R,
Akhmedov M,
Guvenek A,
Cetiner S,
Giaever G,
Iossifov I,
Nislow C,
Shoichet B

Chemistry and Biology
  21 (4): 541-551; Apr 2 2014   NLM
[Abstract]
[DOI] [Full Text]

Reducing INDEL calling errors in whole genome and exome sequencing data
Fang H,
Wu Y,
Narzisi G,
ORawe JA,
Barron LT,
Rosenbaum J,
Ronemus M,
Iossifov I,
Schatz MC,
Lyon GJ

Genome Med
  6 (10): 89; 2014   Nlm
[Abstract]
[DOI] [Full Text]

The role of de novo mutations in the genetics of autism spectrum disorders
Ronemus M,
Iossifov I,
Levy D,
Wigler M

Nature Reviews Genetics
  15 (2): 133-141; 2014  
[Abstract]
[DOI] [Full Text]

Mast-cell leukemia exome sequencing reveals a mutation in the IgE mast-cell receptor beta chain and KIT V654A
Spector MS,
Iossifov I,
Kritharis A,
He C,
Kolitz JE,
Lowe SW,
Allen SL

Leukemia
  26 (6): 1422-1425; Jun 2012  
[DOI] [Full Text]

De novo gene disruptions in children on the autistic spectrum
Iossifov I,
Ronemus M,
Levy D,
Wang Z,
Hakker I,
Rosenbaum J,
Yamrom B,
Lee YH,
Narzisi G,
Leotta A,
Kendall J,
Grabowska E,
Ma B,
Marks S,
Rodgers L,
Stepansky A,
Troge J,
Andrews P,
Bekritsky M,
Pradhan K,
Ghiban E,
Kramer M,
Parla J,
Demeter R,
Fulton LL,
Fulton RS,
Magrini VJ,
Ye K,
Darnell JC,
Darnell RB,
Mardis ER,
Wilson RK,
Schatz MC,
McCombie WR,
Wigler M

Neuron
  74 (2): 285-99; Apr 26 2012   Nlm
[Abstract]
[DOI] [Full Text]

A comparative analysis of exome capture
Parla JS,
Iossifov I,
Grabill I,
Spector MS,
Kramer M,
McCombie WR

Genome Biol
  12 (9): R97; Sep 29 2011   NLM
[Abstract]
[DOI] [Full Text]

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders
Levy D,
Ronemus M,
Yamrom B,
Lee YH,
Leotta A,
Kendall JT,
Marks S,
Lakshmi B,
Pai D,
Ye K,
Buja A,
Krieger A,
Yoon S,
Troge JE,
Rodgers ,
Iossifov I,
Wigler MH

Neuron
  70 (5): 886-897; Jun 8 2011  
[Abstract]
[DOI]

Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses
Gilman S,
Iossifov I,
Levy D,
Ronemus M,
Wigler MH,
Vitkup D

Neuron
  70 (5): 898-907; Jun 8 2011  
[Abstract]
[DOI]

Looking at Cerebellar Malformations through Text-Mined Interactomes of Mice and Humans
Iossifov I,
Rodriguez-Esteban R,
Mayzus I,
Millen KJ,
Rzhetsky A

PLoS Comput Biol
  5 (11): e1000559; Nov 6 2009   PMCID: PMC2767227
[Abstract]
[DOI] [Full Text]

Figure mining for biomedical research
Rodriguez-Esteban R,
Iossifov I

Bioinformatics
  25 (16): 2082-2084; Aug 15 2009  
[Abstract]
[DOI] [Full Text] [PDF]


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