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Refinado por: Base de dados/Biblioteca: AUC Wiley Frozen Package in 2012 remover Nome da Publicação: American Journal Of Medical Genetics remover
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1
Influence of CLOCK gene polymorphism on circadian mood fluctuation and illness recurrence in bipolar depression
Influence of CLOCK gene polymorphism on circadian mood fluctuation and illness recurrence in bipolar depression
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Influence of CLOCK gene polymorphism on circadian mood fluctuation and illness recurrence in bipolar depression

Benedetti, Francesco ; Serretti, Alessandro ; Colombo, Cristina ; Barbini, Barbara ; Lorenzi, Cristina ; Campori, Euridice ; Smeraldi, Enrico

American journal of medical genetics, 2003-11, Vol.123B (1), p.23-26 [Periódico revisado por pares]

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2
Methylomics in psychiatry: Modulation of gene-environment interactions may be through DNA methylation
Methylomics in psychiatry: Modulation of gene-environment interactions may be through DNA methylation
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Methylomics in psychiatry: Modulation of gene-environment interactions may be through DNA methylation

Abdolmaleky, Hamid Mostafavi ; Smith, Cassandra L. ; Faraone, Stephen V. ; Shafa, Rahim ; Stone, William ; Glatt, Stephen J. ; Tsuang, Ming T.

American journal of medical genetics, 2004-05, Vol.127B (1), p.51-59 [Periódico revisado por pares]

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3
D2 dopamine receptor gene in psychiatric and neurologic disorders and its phenotypes
D2 dopamine receptor gene in psychiatric and neurologic disorders and its phenotypes
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D2 dopamine receptor gene in psychiatric and neurologic disorders and its phenotypes

Noble, Ernest P.

American journal of medical genetics, 2003-01, Vol.116B (1), p.103-125 [Periódico revisado por pares]

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4
Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b
Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b
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Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

Weese-Mayer, Debra E. ; Berry-Kravis, Elizabeth M. ; Zhou, Lili ; Maher, Brion S. ; Silvestri, Jean M. ; Curran, Mark E. ; Marazita, Mary L.

American journal of medical genetics, 2003-12, Vol.123A (3), p.267-278 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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5
Maternal and fetal genetic factors account for most of familial aggregation of preeclampsia: A population-based Swedish cohort study
Maternal and fetal genetic factors account for most of familial aggregation of preeclampsia: A population-based Swedish cohort study
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Maternal and fetal genetic factors account for most of familial aggregation of preeclampsia: A population-based Swedish cohort study

Cnattingius, Sven ; Reilly, Marie ; Pawitan, Yudi ; Lichtenstein, Paul

American journal of medical genetics, 2004-11, Vol.130A (4), p.365-371 [Periódico revisado por pares]

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6
Expression of the dopamine transporter gene is regulated by the 3′ UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR
Expression of the dopamine transporter gene is regulated by the 3′ UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR
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Expression of the dopamine transporter gene is regulated by the 3′ UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR

Mill, Jonathan ; Asherson, Philip ; Browes, Clare ; D'Souza, Ursula ; Craig, Ian

American journal of medical genetics, 2002-12, Vol.114 (8), p.975-979 [Periódico revisado por pares]

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7
Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study
Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study
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Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study

Moore, Susan J. ; Green, Jane S. ; Fan, Yanli ; Bhogal, Ashvinder K. ; Dicks, Elizabeth ; Fernandez, Bridget A. ; Stefanelli, Mark ; Murphy, Christopher ; Cramer, Benvon C. ; Dean, John C.S. ; Beales, Philip L. ; Katsanis, Nicholas ; Bassett, Anne S. ; Davidson, William S. ; Parfrey, Patrick S.

American journal of medical genetics, 2005-02, Vol.132A (4), p.352-360 [Periódico revisado por pares]

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8
Multisystem study of 20 older adults with Williams syndrome
Multisystem study of 20 older adults with Williams syndrome
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Multisystem study of 20 older adults with Williams syndrome

Cherniske, Elizabeth M. ; Carpenter, Thomas O. ; Klaiman, Cheryl ; Young, Eytan ; Bregman, Joel ; Insogna, Karl ; Schultz, Robert T. ; Pober, Barbara R.

American journal of medical genetics, 2004-12, Vol.131A (3), p.255-264 [Periódico revisado por pares]

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9
Co-occurrence of ADHD and low IQ has genetic origins
Co-occurrence of ADHD and low IQ has genetic origins
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Co-occurrence of ADHD and low IQ has genetic origins

Kuntsi, J. ; Eley, T.C. ; Taylor, A. ; Hughes, C. ; Asherson, P. ; Caspi, A. ; Moffitt, T.E.

American journal of medical genetics, 2004-01, Vol.124B (1), p.41-47 [Periódico revisado por pares]

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10
The hedgehog signaling network
The hedgehog signaling network
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The hedgehog signaling network

Cohen, Jr, M. Michael

American journal of medical genetics, 2003-11, Vol.123A (1), p.5-28 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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