E-LIB Suche - Ergebnisse für: Coon, H

1

Combined genome-wide linkage and targeted association analy..:

Woodbury-Smith, M. ; Bilder, D. A. ; Morgan, J....
Journal of Neurodevelopmental Disorders. 9 (2017) 1 - p. , 2017

Link: https://doi.org/10.1186/..

2

Acute Air Pollution Exposure and Risk of Suicide Completion:

Bakian, A. V. ; Huber, R. S. ; Coon, H....
American Journal of Epidemiology. 181 (2015) 5 - p. 295-303 , 2015

Link: https://doi.org/10.1093/..

3

Bakian et al. Respond to "Assessing Air Pollution and Suici..:

Bakian, A. V. ; Huber, R. S. ; Coon, H....
American Journal of Epidemiology. 181 (2015) 5 - p. 309-310 , 2015

Link: https://doi.org/10.1093/..

4

Identifying rare variants for genetic risk through a combin..:

Darlington, T M ; Pimentel, R ; Smith, K...
Translational Psychiatry. 4 (2014) 10 - p. e471-e471 , 2014

Link: https://doi.org/10.1038/..

5

SLC6A3 coding variant Ala559Val found in two autism proband..:

Bowton, E ; Saunders, C ; Reddy, I A...
Translational Psychiatry. 4 (2014) 10 - p. e464-e464 , 2014

Link: https://doi.org/10.1038/..

6

Effect of Neuronal Nicotinic Acetylcholine Receptor Genes (..:

Cannon, D. S. ; Mermelstein, R. J. ; Hedeker, D....
Nicotine & Tobacco Research. 16 (2013) 2 - p. 137-144 , 2013

Link: https://doi.org/10.1093/..

7

Genetic risk factors in two Utah pedigrees at high risk for..:

Coon, H ; Darlington, T ; Pimentel, R...
Translational Psychiatry. 3 (2013) 11 - p. e325-e325 , 2013

Link: https://doi.org/10.1038/..

8

Identification of Rare Variants from Exome Sequence in a La..:

Marchani, E.E. ; Chapman, N.H. ; Cheung, C.Y.K....
Human Heredity. 74 (2012) 3-4 - p. 153-164 , 2012

Link: https://doi.org/10.1159/..

9

Identification of Rare Variants from Exome Sequence in a La..:

Marchani, E.E. ; Chapman, N.H. ; Cheung, C.Y.K....
Human Heredity. 74 (2012) 3/4 - p. 153-164 , 2012

Link: https://www.jstor.org/st..

10

An autosomal dominant ataxia maps to 19q13: Allelic heterog..:

Waters, M. F. ; Fee, D. ; Figueroa, K. P....
Neurology. 65 (2005) 7 - p. 1111-1113 , 2005

Link: https://doi.org/10.1212/..

11

Genetic mapping of a novel X-linked recessive colobomatous ..:

Lehman, D.M. ; Sponsel, W.E. ; Stratton, R.F....
American Journal of Medical Genetics. 101 (2001) 2 - p. 114-119 , 2001

Link: https://doi.org/10.1002/..

12

Tryptophan hydroxylase polymorphisms in suicide victims:

Bennett, P. J. ; McMahon, W. M. ; Watabe, J....
Psychiatric Genetics. 10 (2000) 1 - p. 13-17 , 2000

Link: https://doi.org/10.1097/..

13

Mutation screening of a neutral amino acid transporter, ASC..:

Bennett, P. J. ; Hoff, M. ; Rosenthal, J....
Psychiatric Genetics. 10 (2000) 2 - p. 79-82 , 2000

Link: https://doi.org/10.1097/..

14

Haplosufficiency of the melanocortin-4 receptor gene in ind..:

Cody, J.D. ; Reveles, X.T. ; Hale, D.E....
Human Genetics. 105 (1999) 5 - p. 424-427 , 1999

Link: https://doi.org/10.1007/..

15

Evidence for a major gene accounting for mild elevation in ..:

COON, H. ; LEPPERT, M. F. ; KRONENBERG, F....
Annals of Human Genetics. 63 (1999) 5 - p. 401-412 , 1999

Link: https://doi.org/10.1046/..