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Longitudinal study of the profile and predictors of left ventricular mass regression after stentless aortic valve replacement. [electronic resource] by
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- Theodorou, Panagiotis
- Sousa, Ines
- Ashrafian, Hutan
- Chamageorgakis, Themis
- Duncan, Alison
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- Diggle, Peter
- Pepper, John
Producer: 20080612
In:
The Annals of thoracic surgery vol. 85
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Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians. [electronic resource] by
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- Shahram, Farhad
- Francisco, David
- Davatchi, Fereydoun
- Abdollahi, Bahar Sadeghi
- Ghaderibarmi, Fahmida
- Nadji, Abdolhadi
- Mojarad Shafiee, Niloofar
- Xavier, Joana M
- Oliveira, Sofia A
Producer: 20160216
In:
Arthritis & rheumatology (Hoboken, N.J.) vol. 67
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Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. [electronic resource] by
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- Toma, Claudio
- Wilson, Natalie
- Volpi, Emanuela V
- Sousa, Inês
- Pagnamenta, Alistair T
- Tancredi, Raffaella
- Battaglia, Agatino
- Maestrini, Elena
- Bailey, Anthony J
- Monaco, Anthony P
Producer: 20091214
In:
European journal of human genetics : EJHG vol. 17
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Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal. [electronic resource] by
- Abrantes, Patrícia
- Santos, Maria M
- Sousa, Inês
- Xavier, Joana M
- Francisco, Vânia
- Krug, Tiago
- Sobral, João
- Matos, Mafalda
- Martins, Madalena
- Jacinto, António
- Coiteiro, Domingos
- Oliveira, Sofia A
Producer: 20160511
In:
PloS one vol. 10
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FUT2: filling the gap between genes and environment in Behçet's disease? [electronic resource] by
- Xavier, Joana M
- Shahram, Farhad
- Sousa, Inês
- Davatchi, Fereydoun
- Matos, Mafalda
- Abdollahi, Bahar Sadeghi
- Sobral, João
- Nadji, Abdolhadi
- Oliveira, Manuela
- Ghaderibarim, Fahmida
- Shafiee, Niloofar Mojarad
- Oliveira, Sofia A
Producer: 20150511
In:
Annals of the rheumatic diseases vol. 74
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Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels. [electronic resource] by
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- Sousa, Inês
- Martins, Madalena
- Correia, Catarina
- Morgadinho, Teresa
- Bento, Celeste
- Marques, Carla
- Ataíde, Assunção
- Miguel, Teresa S
- Moore, Jason H
- Oliveira, Guiomar
- Vicente, Astrid M
Producer: 20070720
In:
Human genetics vol. 121
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Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. [electronic resource] by
- Sousa, Inês
- Clark, Taane G
- Holt, Richard
- Pagnamenta, Alistair T
- Mulder, Erik J
- Minderaa, Ruud B
- Bailey, Anthony J
- Battaglia, Agatino
- Klauck, Sabine M
- Poustka, Fritz
- Monaco, Anthony P
Producer: 20110714
In:
Molecular autism vol. 1
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MET and autism susceptibility: family and case-control studies. [electronic resource] by
- Sousa, Inês
- Clark, Taane G
- Toma, Claudio
- Kobayashi, Kazuhiro
- Choma, Maja
- Holt, Richard
- Sykes, Nuala H
- Lamb, Janine A
- Bailey, Anthony J
- Battaglia, Agatino
- Maestrini, Elena
- Monaco, Anthony P
Producer: 20090901
In:
European journal of human genetics : EJHG vol. 17
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Assessing dam implementation impact on threatened carnivores: the case of Alqueva in SE Portugal. [electronic resource] by
- Santos, Maria J
- Pedroso, Nuno M
- Ferreira, Joaquim P
- Matos, Hugo M
- Sales-Luís, Teresa
- Pereira, Iris
- Baltazar, Carla
- Grilo, Clara
- Cândido, Ana T
- Sousa, Inês
- Santos-Reis, Margarida
Producer: 20081028
In:
Environmental monitoring and assessment vol. 142
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73.
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Linkage and candidate gene studies of autism spectrum disorders in European populations. [electronic resource] by
- Holt, Richard
- Barnby, Gabrielle
- Maestrini, Elena
- Bacchelli, Elena
- Brocklebank, Denise
- Sousa, Inês
- Mulder, Erik J
- Kantojärvi, Katri
- Järvelä, Irma
- Klauck, Sabine M
- Poustka, Fritz
- Bailey, Anthony J
- Monaco, Anthony P
Producer: 20101202
In:
European journal of human genetics : EJHG vol. 18
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Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax. [electronic resource] by
- Sousa, Inês
- Abrantes, Patrícia
- Francisco, Vânia
- Teixeira, Gilberto
- Monteiro, Marta
- Neves, João
- Norte, Ana
- Robalo Cordeiro, Carlos
- Moura E Sá, João
- Reis, Ernestina
- Santos, Patrícia
- Oliveira, Manuela
- Sousa, Susana
- Fradinho, Marta
- Malheiro, Filipa
- Negrão, Luís
- Feijó, Salvato
- Oliveira, Sofia A
Producer: 20170710
In:
PloS one vol. 11
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IL10 low-frequency variants in Behçet's disease patients. [electronic resource] by
- Matos, Mafalda
- Xavier, Joana M
- Abrantes, Patrícia
- Sousa, Inês
- Rei, Nádia
- Davatchi, Fereydoun
- Shahram, Farhad
- Jesus, Gorete
- Barcelos, Filipe
- Vedes, Joana
- Salgado, Manuel
- Abdollahi, Bahar Sadeghi
- Nadji, Abdolhadi
- Moraes-Fontes, Maria Francisca
- Shafiee, Niloofar Mojarad
- Ghaderibarmi, Fahmida
- Vaz Patto, José
- Crespo, Jorge
- Oliveira, Sofia A
Producer: 20180402
In:
International journal of rheumatic diseases vol. 20
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Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders. [electronic resource] by
- Correia, Catarina T
- Conceição, Inês C
- Oliveira, Bárbara
- Coelho, Joana
- Sousa, Inês
- Sequeira, Ana F
- Almeida, Joana
- Café, Cátia
- Duque, Frederico
- Mouga, Susana
- Roberts, Wendy
- Gao, Kun
- Lowe, Jennifer K
- Thiruvahindrapuram, Bhooma
- Walker, Susan
- Marshall, Christian R
- Pinto, Dalila
- Nurnberger, John I
- Scherer, Stephen W
- Geschwind, Daniel H
- Oliveira, Guiomar
- Vicente, Astrid M
Producer: 20140416
In:
Molecular autism vol. 5
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Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility. [electronic resource] by
- Takeuchi, Masaki
- Mizuki, Nobuhisa
- Meguro, Akira
- Ombrello, Michael J
- Kirino, Yohei
- Satorius, Colleen
- Le, Julie
- Blake, Mary
- Erer, Burak
- Kawagoe, Tatsukata
- Ustek, Duran
- Tugal-Tutkun, Ilknur
- Seyahi, Emire
- Ozyazgan, Yilmaz
- Sousa, Inês
- Davatchi, Fereydoun
- Francisco, Vânia
- Shahram, Farhad
- Abdollahi, Bahar Sadeghi
- Nadji, Abdolhadi
- Shafiee, Niloofar Mojarad
- Ghaderibarmi, Fahmida
- Ohno, Shigeaki
- Ueda, Atsuhisa
- Ishigatsubo, Yoshiaki
- Gadina, Massimo
- Oliveira, Sofia A
- Gül, Ahmet
- Kastner, Daniel L
- Remmers, Elaine F
Producer: 20170905
In:
Nature genetics vol. 49
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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. [electronic resource] by
- Casey, Jillian P
- Magalhaes, Tiago
- Conroy, Judith M
- Regan, Regina
- Shah, Naisha
- Anney, Richard
- Shields, Denis C
- Abrahams, Brett S
- Almeida, Joana
- Bacchelli, Elena
- Bailey, Anthony J
- Baird, Gillian
- Battaglia, Agatino
- Berney, Tom
- Bolshakova, Nadia
- Bolton, Patrick F
- Bourgeron, Thomas
- Brennan, Sean
- Cali, Phil
- Correia, Catarina
- Corsello, Christina
- Coutanche, Marc
- Dawson, Geraldine
- de Jonge, Maretha
- Delorme, Richard
- Duketis, Eftichia
- Duque, Frederico
- Estes, Annette
- Farrar, Penny
- Fernandez, Bridget A
- Folstein, Susan E
- Foley, Suzanne
- Fombonne, Eric
- Freitag, Christine M
- Gilbert, John
- Gillberg, Christopher
- Glessner, Joseph T
- Green, Jonathan
- Guter, Stephen J
- Hakonarson, Hakon
- Holt, Richard
- Hughes, Gillian
- Hus, Vanessa
- Igliozzi, Roberta
- Kim, Cecilia
- Klauck, Sabine M
- Kolevzon, Alexander
- Lamb, Janine A
- Leboyer, Marion
- Le Couteur, Ann
- Leventhal, Bennett L
- Lord, Catherine
- Lund, Sabata C
- Maestrini, Elena
- Mantoulan, Carine
- Marshall, Christian R
- McConachie, Helen
- McDougle, Christopher J
- McGrath, Jane
- McMahon, William M
- Merikangas, Alison
- Miller, Judith
- Minopoli, Fiorella
- Mirza, Ghazala K
- Munson, Jeff
- Nelson, Stanley F
- Nygren, Gudrun
- Oliveira, Guiomar
- Pagnamenta, Alistair T
- Papanikolaou, Katerina
- Parr, Jeremy R
- Parrini, Barbara
- Pickles, Andrew
- Pinto, Dalila
- Piven, Joseph
- Posey, David J
- Poustka, Annemarie
- Poustka, Fritz
- Ragoussis, Jiannis
- Roge, Bernadette
- Rutter, Michael L
- Sequeira, Ana F
- Soorya, Latha
- Sousa, Inês
- Sykes, Nuala
- Stoppioni, Vera
- Tancredi, Raffaella
- Tauber, Maïté
- Thompson, Ann P
- Thomson, Susanne
- Tsiantis, John
- Van Engeland, Herman
- Vincent, John B
- Volkmar, Fred
- Vorstman, Jacob A S
- Wallace, Simon
- Wang, Kai
- Wassink, Thomas H
- White, Kathy
- Wing, Kirsty
- Wittemeyer, Kerstin
- Yaspan, Brian L
- Zwaigenbaum, Lonnie
- Betancur, Catalina
- Buxbaum, Joseph D
- Cantor, Rita M
- Cook, Edwin H
- Coon, Hilary
- Cuccaro, Michael L
- Geschwind, Daniel H
- Haines, Jonathan L
- Hallmayer, Joachim
- Monaco, Anthony P
- Nurnberger, John I
- Pericak-Vance, Margaret A
- Schellenberg, Gerard D
- Scherer, Stephen W
- Sutcliffe, James S
- Szatmari, Peter
- Vieland, Veronica J
- Wijsman, Ellen M
- Green, Andrew
- Gill, Michael
- Gallagher, Louise
- Vicente, Astrid
- Ennis, Sean
Producer: 20120514
In:
Human genetics vol. 131
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80.
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Individual common variants exert weak effects on the risk for autism spectrum disorders. [electronic resource] by
- Anney, Richard
- Klei, Lambertus
- Pinto, Dalila
- Almeida, Joana
- Bacchelli, Elena
- Baird, Gillian
- Bolshakova, Nadia
- Bölte, Sven
- Bolton, Patrick F
- Bourgeron, Thomas
- Brennan, Sean
- Brian, Jessica
- Casey, Jillian
- Conroy, Judith
- Correia, Catarina
- Corsello, Christina
- Crawford, Emily L
- de Jonge, Maretha
- Delorme, Richard
- Duketis, Eftichia
- Duque, Frederico
- Estes, Annette
- Farrar, Penny
- Fernandez, Bridget A
- Folstein, Susan E
- Fombonne, Eric
- Gilbert, John
- Gillberg, Christopher
- Glessner, Joseph T
- Green, Andrew
- Green, Jonathan
- Guter, Stephen J
- Heron, Elizabeth A
- Holt, Richard
- Howe, Jennifer L
- Hughes, Gillian
- Hus, Vanessa
- Igliozzi, Roberta
- Jacob, Suma
- Kenny, Graham P
- Kim, Cecilia
- Kolevzon, Alexander
- Kustanovich, Vlad
- Lajonchere, Clara M
- Lamb, Janine A
- Law-Smith, Miriam
- Leboyer, Marion
- Le Couteur, Ann
- Leventhal, Bennett L
- Liu, Xiao-Qing
- Lombard, Frances
- Lord, Catherine
- Lotspeich, Linda
- Lund, Sabata C
- Magalhaes, Tiago R
- Mantoulan, Carine
- McDougle, Christopher J
- Melhem, Nadine M
- Merikangas, Alison
- Minshew, Nancy J
- Mirza, Ghazala K
- Munson, Jeff
- Noakes, Carolyn
- Nygren, Gudrun
- Papanikolaou, Katerina
- Pagnamenta, Alistair T
- Parrini, Barbara
- Paton, Tara
- Pickles, Andrew
- Posey, David J
- Poustka, Fritz
- Ragoussis, Jiannis
- Regan, Regina
- Roberts, Wendy
- Roeder, Kathryn
- Roge, Bernadette
- Rutter, Michael L
- Schlitt, Sabine
- Shah, Naisha
- Sheffield, Val C
- Soorya, Latha
- Sousa, Inês
- Stoppioni, Vera
- Sykes, Nuala
- Tancredi, Raffaella
- Thompson, Ann P
- Thomson, Susanne
- Tryfon, Ana
- Tsiantis, John
- Van Engeland, Herman
- Vincent, John B
- Volkmar, Fred
- Vorstman, J A S
- Wallace, Simon
- Wing, Kirsty
- Wittemeyer, Kerstin
- Wood, Shawn
- Zurawiecki, Danielle
- Zwaigenbaum, Lonnie
- Bailey, Anthony J
- Battaglia, Agatino
- Cantor, Rita M
- Coon, Hilary
- Cuccaro, Michael L
- Dawson, Geraldine
- Ennis, Sean
- Freitag, Christine M
- Geschwind, Daniel H
- Haines, Jonathan L
- Klauck, Sabine M
- McMahon, William M
- Maestrini, Elena
- Miller, Judith
- Monaco, Anthony P
- Nelson, Stanley F
- Nurnberger, John I
- Oliveira, Guiomar
- Parr, Jeremy R
- Pericak-Vance, Margaret A
- Piven, Joseph
- Schellenberg, Gerard D
- Scherer, Stephen W
- Vicente, Astrid M
- Wassink, Thomas H
- Wijsman, Ellen M
- Betancur, Catalina
- Buxbaum, Joseph D
- Cook, Edwin H
- Gallagher, Louise
- Gill, Michael
- Hallmayer, Joachim
- Paterson, Andrew D
- Sutcliffe, James S
- Szatmari, Peter
- Vieland, Veronica J
- Hakonarson, Hakon
- Devlin, Bernie
Producer: 20130403
In:
Human molecular genetics vol. 21
Availability: No items available.
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