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5 Article(s) on File
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SeqHBase: a big data toolset for family based sequencing data analysis
He M,
Person TN,
Hebbring SJ,
Heinzen E,
Ye Z,
Schrodi SJ,
McPherson EW,
Lin SM,
Peissig PL,
Brilliant MH,
ORawe J,
Robison RJ,
Lyon GJ,
Wang K

J Med Genet
  (0): Jan 13 2015   Nlm
[Abstract]
[DOI] [Full Text]

Integrating precision medicine in the study and clinical treatment of a severely mentally ill person
ORawe JA,
Fang H,
Rynearson S,
Robison R,
Kiruluta ES,
Higgins G,
Eilbeck K,
Reese MG,
Lyon GJ

PeerJ
  1 (0): Oct 3 2013   NLM
[Abstract]
[DOI] [Full Text]

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
Elia J,
Glessner JT,
Wang K,
Takahashi N,
Shtir CJ,
Hadley D,
Sleiman PM,
Zhang H,
Kim CE,
Robison R,
Lyon GJ,
Flory JH,
Bradfield JP,
Imielinski M,
Hou C,
Frackelton EC,
Chiavacci RM,
Sakurai T,
Rabin C,
Middleton FA,
Thomas KA,
Garris M,
Mentch F,
Freitag CM,
Steinhausen HC,
Todorov AA,
Reif A,
Rothenberger A,
Franke B,
Mick EO,
Roeyers H,
Buitelaar J,
Lesch KP,
Banaschewski T,
Ebstein RP,
Mulas F,
Oades RD,
Sergeant J,
Sonuga-Barke E,
Renner TJ,
Romanos M,
Romanos J,
Warnke A,
Walitza S,
Meyer J,
Pálmason H,
Seitz C,
Loo SK,
Smalley SL,
Biederman J,
Kent L,
Asherson P,
Anney RJ,
Gaynor JW,
Shaw P,
Devoto M,
White PS,
Grant SF,
Buxbaum JD,
Rapoport JL,
Williams NM,
Nelson SF,
Faraone SV,
Hakonarson H

Nature Genetics
  44 (1): 78-84; Dec 4 2012  
[Abstract]
[DOI] [Full Text]

Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43))
Rope AF,
Wang K,
Evjenth R,
Xing J,
Johnston JJ,
Swensen JJ,
Johnson WE,
Moore B,
Huff CD,
Bird LM,
Carey JC,
Opitz JM,
Stevens CA,
Jiang T,
Schank C,
Fain HD,
Robison R,
Dalley B,
Chin S,
South ST,
Pysher TJ,
Jorde LB,
Hakonarson H,
Lillehaug JR,
Biesecker LG,
Yandell M,
Arnesen T,
Lyon GJ

Am J Hum Genet
  89 (2): 345; Aug 12 2011  
[DOI]

The Use of Emotional Dysregulation as an Endophenotype for Genetic studies in Adults with Attention-Deficit Hyperactivity Disorder
Robison RJ,
Reimherr FW,
Marchant BK,
Kondo D,
Lyon GJ,
Olsen J,
Christopherson D,
Pommerville C,
Tuya S,
Johnson A,
Coon H

Journal of ADHD and Related Disorders
  1 (4): 29-38; 2010  
[Full Text]


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