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Biological Psychiatry

Volumn 77, Issue 9, 2015, Pages 769-771

Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism"

(2) Duyzend, Michael H a Eichler, Evan E a

a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; CHROMOSOME 16P; CHROMOSOME DELETION; COMPULSION; DEVELOPMENTAL COORDINATION DISORDER; GENOTYPE; HUMAN; INTELLIGENCE QUOTIENT; NOTE; PHENOTYPE; PRIORITY JOURNAL; SOCIAL STATUS; CHROMOSOME 16; COGNITION; DEVELOPMENTAL DISORDER; GENETICS; MENTAL DISEASE;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; COGNITION; DEVELOPMENTAL DISABILITIES; HUMANS; MENTAL DISORDERS; PHENOTYPE;

EID: 84926353337 PISSN: 00063223 EISSN: 18732402 Source Type: Journal
DOI: 10.1016/j.biopsych.2015.02.032 Document Type: Note

Times cited : (11)

References (10)

1
- 84926373318
- The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population
- E. Hanson, R. Bernier, K. Porche, F.I. Jackson, R.P. Goin-Kochel, and L.G. Snyder The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population Biol Psychiatry 77 2015 785 793
- (2015) Biol Psychiatry , vol.77 , pp. 785-793
- Hanson, E.¹ Bernier, R.² Porche, K.³ Jackson, F.I.⁴ Goin-Kochel, R.P.⁵ Snyder, L.G.⁶

2
- 39049163023
- Association between microdeletion and microduplication at 16p11.2 and autism
- L.A. Weiss, Y. Shen, J.M. Korn, D.E. Arking, D.T. Miller, and R. Fossdal Association between microdeletion and microduplication at 16p11.2 and autism N Engl J Med 358 2008 667 675
- (2008) N Engl J Med , vol.358 , pp. 667-675
- Weiss, L.A.¹ Shen, Y.² Korn, J.M.³ Arking, D.E.⁴ Miller, D.T.⁵ Fossdal, R.⁶

3
- 38849126088
- Recurrent 16p11.2 microdeletions in autism
- R.A. Kumar, S. KaraMohamed, J. Sudi, D.F. Conrad, C. Brune, and J.A. Badner Recurrent 16p11.2 microdeletions in autism Hum Mol Genet 17 2008 628 638
- (2008) Hum Mol Genet , vol.17 , pp. 628-638
- Kumar, R.A.¹ Karamohamed, S.² Sudi, J.³ Conrad, D.F.⁴ Brune, C.⁵ Badner, J.A.⁶

4
- 77953704493
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
- M. Shinawi, P. Liu, S-H.L. Kang, J. Shen, J.W. Belmont, and D.A. Scott Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size J Med Genet 47 2010 332 341
- (2010) J Med Genet , vol.47 , pp. 332-341
- Shinawi, M.¹ Liu, P.² Kang, S.-H.L.³ Shen, J.⁴ Belmont, J.W.⁵ Scott, D.A.⁶

5
- 84870280744
- A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
- F. Zufferey, E.H. Sherr, N.D. Beckmann, E. Hanson, A.M. Maillard, and L. Hippolyte A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders J Med Genet 49 2012 660 668
- (2012) J Med Genet , vol.49 , pp. 660-668
- Zufferey, F.¹ Sherr, E.H.² Beckmann, N.D.³ Hanson, E.⁴ Maillard, A.M.⁵ Hippolyte, L.⁶

6
- 84892620880
- CNVs conferring risk of autism or schizophrenia affect cognition in controls
- H. Stefansson, A. Meyer-Lindenberg, S. Steinberg, B. Magnusdottir, K. Morgen, and S. Arnarsdottir CNVs conferring risk of autism or schizophrenia affect cognition in controls Nature 505 2014 361 366
- (2014) Nature , vol.505 , pp. 361-366
- Stefansson, H.¹ Meyer-Lindenberg, A.² Steinberg, S.³ Magnusdottir, B.⁴ Morgen, K.⁵ Arnarsdottir, S.⁶

7
- 0028224352
- Cerebral asymmetry and handedness
- L.E. White, G. Lucas, A. Richards, and D. Purves Cerebral asymmetry and handedness Nature 368 1994 197 198
- (1994) Nature , vol.368 , pp. 197-198
- White, L.E.¹ Lucas, G.² Richards, A.³ Purves, D.⁴

8
- 84896829795
- A genotype-first approach to defining the subtypes of a complex disease
- H.A. Stessman, R. Bernier, and E.E. Eichler A genotype-first approach to defining the subtypes of a complex disease Cell 156 2014 872 877
- (2014) Cell , vol.156 , pp. 872-877
- Stessman, H.A.¹ Bernier, R.² Eichler, E.E.³

9
- 84904635209
- Disruptive CHD8 mutations define a subtype of autism early in development
- R. Bernier, C. Golzio, B. Xiong, H.A. Stessman, B.P. Coe, and O. Penn Disruptive CHD8 mutations define a subtype of autism early in development Cell 158 2014 263 276
- (2014) Cell , vol.158 , pp. 263-276
- Bernier, R.¹ Golzio, C.² Xiong, B.³ Stessman, H.A.⁴ Coe, B.P.⁵ Penn, O.⁶

10
- 84858673064
- Simons Variation in Individuals Project (Simons VIP): A genetics-first approach to studying autism spectrum and related neurodevelopmental disorders
- Simons VIP Consortium
- Simons VIP Consortium Simons Variation in Individuals Project (Simons VIP): A genetics-first approach to studying autism spectrum and related neurodevelopmental disorders Neuron 73 2012 1063 1067
- (2012) Neuron , vol.73 , pp. 1063-1067

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.