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- Avramopoulos, D
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Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients. [electronic resource] by
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- Nestadt, G
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Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis. [electronic resource] by
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A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM. [electronic resource] by
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- Brahe, C
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Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter. [electronic resource] by
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- Kitsos, G
- Vassilopoulos, D
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Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans. [electronic resource] by
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- Freeman, S B
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- Torfs, C
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Tetrasomy 18p de novo: parental origin and different mechanisms of formation. [electronic resource] by
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- Sarri, C
- Avramopoulos, D
- Kitsiou, S
- Lambert, J C
- Guzda, M
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Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. [electronic resource] by
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- Gu, Y
- Hallberg, A
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- Pettay, D
- Saker, D
- Shen, J
- Taft, L
- Mikkelsen, M
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- Hassold, T
- Sherman, S L
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Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. [electronic resource] by
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- Hersey, J
- Gu, Y
- Shen, J
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- May, K M
- Avramopoulos, D
- Petersen, M B
- Hallberg, A
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Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism. [electronic resource] by
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- Grigoriadou, M
- Albrecht, B
- Passarge, E
- Annerén, G
- Blennow, E
- Clausen, N
- Galla-Voumvouraki, A
- Tsezou, A
- Kitsiou-Tzeli, S
- Hahnemann, J M
- Hertz, J M
- Houge, G
- Kuklík, M
- Macek, M
- Lacombe, D
- Miller, K
- Moncla, A
- López Pajares, I
- Patsalis, P C
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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. [electronic resource] by
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- Knowles, E
- Davies, G
- Liewald, D C
- Starr, J M
- Djurovic, S
- Melle, I
- Sundet, K
- Christoforou, A
- Reinvang, I
- DeRosse, P
- Lundervold, A J
- Steen, V M
- Espeseth, T
- Räikkönen, K
- Widen, E
- Palotie, A
- Eriksson, J G
- Giegling, I
- Konte, B
- Roussos, P
- Giakoumaki, S
- Burdick, K E
- Payton, A
- Ollier, W
- Horan, M
- Chiba-Falek, O
- Attix, D K
- Need, A C
- Cirulli, E T
- Voineskos, A N
- Stefanis, N C
- Avramopoulos, D
- Hatzimanolis, A
- Arking, D E
- Smyrnis, N
- Bilder, R M
- Freimer, N A
- Cannon, T D
- London, E
- Poldrack, R A
- Sabb, F W
- Congdon, E
- Conley, E D
- Scult, M A
- Dickinson, D
- Straub, R E
- Donohoe, G
- Morris, D
- Corvin, A
- Gill, M
- Hariri, A R
- Weinberger, D R
- Pendleton, N
- Bitsios, P
- Rujescu, D
- Lahti, J
- Le Hellard, S
- Keller, M C
- Andreassen, O A
- Deary, I J
- Glahn, D C
- Malhotra, A K
- Lencz, T
Producer: 20171002
In:
Molecular psychiatry vol. 22
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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. [electronic resource] by
- Trampush, J W
- Yang, M L Z
- Yu, J
- Knowles, E
- Davies, G
- Liewald, D C
- Starr, J M
- Djurovic, S
- Melle, I
- Sundet, K
- Christoforou, A
- Reinvang, I
- DeRosse, P
- Lundervold, A J
- Steen, V M
- Espeseth, T
- Räikkönen, K
- Widen, E
- Palotie, A
- Eriksson, J G
- Giegling, I
- Konte, B
- Roussos, P
- Giakoumaki, S
- Burdick, K E
- Payton, A
- Ollier, W
- Horan, M
- Chiba-Falek, O
- Attix, D K
- Need, A C
- Cirulli, E T
- Voineskos, A N
- Stefanis, N C
- Avramopoulos, D
- Hatzimanolis, A
- Arking, D E
- Smyrnis, N
- Bilder, R M
- Freimer, N A
- Cannon, T D
- London, E
- Poldrack, R A
- Sabb, F W
- Congdon, E
- Conley, E D
- Scult, M A
- Dickinson, D
- Straub, R E
- Donohoe, G
- Morris, D
- Corvin, A
- Gill, M
- Hariri, A R
- Weinberger, D R
- Pendleton, N
- Bitsios, P
- Rujescu, D
- Lahti, J
- Le Hellard, S
- Keller, M C
- Andreassen, O A
- Deary, I J
- Glahn, D C
- Malhotra, A K
- Lencz, T
Publication details: Molecular psychiatry 11 2017
In:
Molecular psychiatry vol. 22
Availability: No items available.
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