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Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations. [electronic resource] by
- Granados-Riveron, Javier T
- Pope, Mark
- Bu'lock, Frances A
- Thornborough, Christopher
- Eason, Jacqueline
- Setchfield, Kerry
- Ketley, Ami
- Kirk, Edwin P
- Fatkin, Diane
- Feneley, Michael P
- Harvey, Richard P
- Brook, J David
Producer: 20120724
In:
Congenital heart disease vol. 7
Availability: No items available.
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9.
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Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot. [electronic resource] by
- Palomino Doza, Julian
- Topf, Ana
- Bentham, Jamie
- Bhattacharya, Shoumo
- Cosgrove, Catherine
- Brook, J David
- Granados-Riveron, Javier
- Bu'Lock, Frances A
- O'Sullivan, John
- Stuart, A Graham
- Parsons, Jonathan
- Relton, Caroline
- Goodship, Judith
- Henderson, Deborah J
- Keavney, Bernard
Producer: 20131017
In:
BMC genetics vol. 14
Availability: No items available.
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10.
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A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot. [electronic resource] by
- Goodship, Judith A
- Hall, Darroch
- Topf, Ana
- Mamasoula, Chrysovalanto
- Griffin, Helen
- Rahman, Thahira J
- Glen, Elise
- Tan, Huay
- Palomino Doza, Julian
- Relton, Caroline L
- Bentham, Jamie
- Bhattacharya, Shoumo
- Cosgrove, Catherine
- Brook, David
- Granados-Riveron, Javier
- Bu'Lock, Frances A
- O'Sullivan, John
- Stuart, A Graham
- Parsons, Jonathan
- Cordell, Heather J
- Keavney, Bernard
Producer: 20121022
In:
Circulation. Cardiovascular genetics vol. 5
Availability: No items available.
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11.
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Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. [electronic resource] by
- Griffin, Helen R
- Hall, Darroch H
- Topf, Ana
- Eden, James
- Stuart, A Graham
- Parsons, Jonathan
- Peart, Ian
- Deanfield, John E
- O'Sullivan, John
- Babu-Narayan, Sonya V
- Gatzoulis, Michael A
- Bu'lock, Frances A
- Bhattacharya, Shoumo
- Bentham, Jamie
- Farrall, Martin
- Granados Riveron, Javier
- Brook, J David
- Burn, John
- Cordell, Heather J
- Goodship, Judith A
- Keavney, Bernard
Producer: 20090701
In:
PloS one vol. 4
Availability: No items available.
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12.
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Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. [electronic resource] by
- Cordell, Heather J
- Töpf, Ana
- Mamasoula, Chrysovalanto
- Postma, Alex V
- Bentham, Jamie
- Zelenika, Diana
- Heath, Simon
- Blue, Gillian
- Cosgrove, Catherine
- Granados Riveron, Javier
- Darlay, Rebecca
- Soemedi, Rachel
- Wilson, Ian J
- Ayers, Kristin L
- Rahman, Thahira J
- Hall, Darroch
- Mulder, Barbara J M
- Zwinderman, Aelko H
- van Engelen, Klaartje
- Brook, J David
- Setchfield, Kerry
- Bu'Lock, Frances A
- Thornborough, Chris
- O'Sullivan, John
- Stuart, A Graham
- Parsons, Jonathan
- Bhattacharya, Shoumo
- Winlaw, David
- Mital, Seema
- Gewillig, Marc
- Breckpot, Jeroen
- Devriendt, Koen
- Moorman, Antoon F M
- Rauch, Anita
- Lathrop, G Mark
- Keavney, Bernard D
- Goodship, Judith A
Producer: 20130828
In:
Human molecular genetics vol. 22
Availability: No items available.
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13.
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Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. [electronic resource] by
- Page, Donna J
- Miossec, Matthieu J
- Williams, Simon G
- Monaghan, Richard M
- Fotiou, Elisavet
- Cordell, Heather J
- Sutcliffe, Louise
- Topf, Ana
- Bourgey, Mathieu
- Bourque, Guillaume
- Eveleigh, Robert
- Dunwoodie, Sally L
- Winlaw, David S
- Bhattacharya, Shoumo
- Breckpot, Jeroen
- Devriendt, Koenraad
- Gewillig, Marc
- Brook, J David
- Setchfield, Kerry J
- Bu'Lock, Frances A
- O'Sullivan, John
- Stuart, Graham
- Bezzina, Connie R
- Mulder, Barbara J M
- Postma, Alex V
- Bentham, James R
- Baron, Martin
- Bhaskar, Sanjeev S
- Black, Graeme C
- Newman, William G
- Hentges, Kathryn E
- Lathrop, G Mark
- Santibanez-Koref, Mauro
- Keavney, Bernard D
Producer: 20191209
In:
Circulation research vol. 124
Availability: No items available.
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14.
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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. [electronic resource] by
- Al Turki, Saeed
- Manickaraj, Ashok K
- Mercer, Catherine L
- Gerety, Sebastian S
- Hitz, Marc-Phillip
- Lindsay, Sarah
- D'Alessandro, Lisa C A
- Swaminathan, G Jawahar
- Bentham, Jamie
- Arndt, Anne-Karin
- Louw, Jacoba
- Breckpot, Jeroen
- Gewillig, Marc
- Thienpont, Bernard
- Abdul-Khaliq, Hashim
- Harnack, Christine
- Hoff, Kirstin
- Kramer, Hans-Heiner
- Schubert, Stephan
- Siebert, Reiner
- Toka, Okan
- Cosgrove, Catherine
- Watkins, Hugh
- Lucassen, Anneke M
- O'Kelly, Ita M
- Salmon, Anthony P
- Bu'Lock, Frances A
- Granados-Riveron, Javier
- Setchfield, Kerry
- Thornborough, Chris
- Brook, J David
- Mulder, Barbara
- Klaassen, Sabine
- Bhattacharya, Shoumo
- Devriendt, Koen
- FitzPatrick, David R
- Wilson, David I
- Mital, Seema
- Hurles, Matthew E
Publication details: American journal of human genetics Mar 2016
In:
American journal of human genetics vol. 98
Availability: No items available.
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15.
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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. [electronic resource] by
- Cordell, Heather J
- Bentham, Jamie
- Topf, Ana
- Zelenika, Diana
- Heath, Simon
- Mamasoula, Chrysovalanto
- Cosgrove, Catherine
- Blue, Gillian
- Granados-Riveron, Javier
- Setchfield, Kerry
- Thornborough, Chris
- Breckpot, Jeroen
- Soemedi, Rachel
- Martin, Ruairidh
- Rahman, Thahira J
- Hall, Darroch
- van Engelen, Klaartje
- Moorman, Antoon F M
- Zwinderman, Aelko H
- Barnett, Phil
- Koopmann, Tamara T
- Adriaens, Michiel E
- Varro, Andras
- George, Alfred L
- dos Remedios, Christobal
- Bishopric, Nanette H
- Bezzina, Connie R
- O'Sullivan, John
- Gewillig, Marc
- Bu'Lock, Frances A
- Winlaw, David
- Bhattacharya, Shoumo
- Devriendt, Koen
- Brook, J David
- Mulder, Barbara J M
- Mital, Seema
- Postma, Alex V
- Lathrop, G Mark
- Farrall, Martin
- Goodship, Judith A
- Keavney, Bernard D
Producer: 20130910
In:
Nature genetics vol. 45
Availability: No items available.
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16.
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Rare variants in NR2F2 cause congenital heart defects in humans. [electronic resource] by
- Al Turki, Saeed
- Manickaraj, Ashok K
- Mercer, Catherine L
- Gerety, Sebastian S
- Hitz, Marc-Phillip
- Lindsay, Sarah
- D'Alessandro, Lisa C A
- Swaminathan, G Jawahar
- Bentham, Jamie
- Arndt, Anne-Karin
- Louw, Jacoba
- Low, Jacoba
- Breckpot, Jeroen
- Gewillig, Marc
- Thienpont, Bernard
- Abdul-Khaliq, Hashim
- Harnack, Christine
- Hoff, Kirstin
- Kramer, Hans-Heiner
- Schubert, Stephan
- Siebert, Reiner
- Toka, Okan
- Cosgrove, Catherine
- Watkins, Hugh
- Lucassen, Anneke M
- O'Kelly, Ita M
- Salmon, Anthony P
- Bu'lock, Frances A
- Granados-Riveron, Javier
- Setchfield, Kerry
- Thornborough, Chris
- Brook, J David
- Mulder, Barbara
- Klaassen, Sabine
- Bhattacharya, Shoumo
- Devriendt, Koen
- Fitzpatrick, David F
- Wilson, David I
- Mital, Seema
- Hurles, Matthew E
Producer: 20140530
In:
American journal of human genetics vol. 94
Availability: No items available.
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17.
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Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls. [electronic resource] by
- Mamasoula, Chrysovalanto
- Prentice, R Reid
- Pierscionek, Tomasz
- Pangilinan, Faith
- Mills, James L
- Druschel, Charlotte
- Pass, Kenneth
- Russell, Mark W
- Hall, Darroch
- Töpf, Ana
- Brown, Danielle L
- Zelenika, Diana
- Bentham, Jamie
- Cosgrove, Catherine
- Bhattacharya, Shoumo
- Riveron, Javier Granados
- Setchfield, Kerry
- Brook, J David
- Bu'Lock, Frances A
- Thornborough, Chris
- Rahman, Thahira J
- Doza, Julian Palomino
- Tan, Huay L
- O'Sullivan, John
- Stuart, A Graham
- Blue, Gillian
- Winlaw, David
- Postma, Alex V
- Mulder, Barbara J M
- Zwinderman, Aelko H
- van Engelen, Klaartje
- Moorman, Antoon F M
- Rauch, Anita
- Gewillig, Marc
- Breckpot, Jeroen
- Devriendt, Koen
- Lathrop, G Mark
- Farrall, Martin
- Goodship, Judith A
- Cordell, Heather J
- Brody, Lawrence C
- Keavney, Bernard D
Producer: 20140331
In:
Circulation. Cardiovascular genetics vol. 6
Availability: No items available.
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18.
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A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. [electronic resource] by
- Hanchard, Neil A
- Swaminathan, Shanker
- Bucasas, Kristine
- Furthner, Dieter
- Fernbach, Susan
- Azamian, Mahshid S
- Wang, Xueqing
- Lewin, Mark
- Towbin, Jeffrey A
- D'Alessandro, Lisa C A
- Morris, Shaine A
- Dreyer, William
- Denfield, Susan
- Ayres, Nancy A
- Franklin, Wayne J
- Justino, Henri
- Lantin-Hermoso, M Regina
- Ocampo, Elena C
- Santos, Alexia B
- Parekh, Dhaval
- Moodie, Douglas
- Jeewa, Aamir
- Lawrence, Emily
- Allen, Hugh D
- Penny, Daniel J
- Fraser, Charles D
- Lupski, James R
- Popoola, Mojisola
- Wadhwa, Lalita
- Brook, J David
- Bu'Lock, Frances A
- Bhattacharya, Shoumo
- Lalani, Seema R
- Zender, Gloria A
- Fitzgerald-Butt, Sara M
- Bowman, Jessica
- Corsmeier, Don
- White, Peter
- Lecerf, Kelsey
- Zapata, Gladys
- Hernandez, Patricia
- Goodship, Judith A
- Garg, Vidu
- Keavney, Bernard D
- Leal, Suzanne M
- Cordell, Heather J
- Belmont, John W
- McBride, Kim L
Producer: 20170925
In:
Human molecular genetics vol. 25
Availability: No items available.
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