Gregory Costain: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Joint modelling of goals and bookings in association football

Titman, A. C., Costain, D. A., Ridall, P. G., Gregory, K.

Journal:

Journal of the Royal Statistical Society Series A (General)

Year:

2015

Language:

english

File:

PDF, 1.28 MB

english, 2015

2

Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac disease

Costain, Gregory, Roche, S. Lucy, Scherer, Stephen W., Silversides, Candice K., Bassett, Anne S.

Journal:

International Journal of Cardiology

Year:

2016

Language:

english

File:

PDF, 470 KB

english, 2016

3

A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome

Curtis, Meredith, Baribeau, Danielle, Walker, Susan, Carter, Melissa, Costain, Gregory, Lamoureux, Sylvia, Liston, Eriskay, Marshall, Christian R., Reuter, Miriam S., Snell, Meaghan, Summers, Jane, Vo

Journal:

American Journal of Medical Genetics Part A

Year:

2020

File:

PDF, 1.22 MB

2020

4

Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: A preliminary report

Gregory Costain, Andrew Ho, Adrian P. Crawley, David J. Mikulis, Linda M. Brzustowicz, Eva W.C. Chow, Anne S. Bassett

Journal:

Schizophrenia Research

Year:

2010

Language:

english

File:

PDF, 331 KB

english, 2010

5

Genome-wide sequencing expands the phenotypic spectrum of EP300 variants

Costain, Gregory, Kannu, Peter, Bowdin, Sarah

Journal:

European Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 759 KB

english, 2017

6

Prenatal Genetic Testing With Chromosomal Microarray Analysis Identifies Major Risk Variants for Schizophrenia and Other Later-Onset Disorders

Costain, Gregory, McDonald-McGinn, Donna M., Bassett, Anne S.

Journal:

American Journal of Psychiatry

Year:

2013

Language:

english

File:

PDF, 450 KB

english, 2013

7

Clinical Application of Targeted Next-Generation Sequencing Panels and Whole Exome Sequencing in Childhood Epilepsy

Costain, Gregory, Cordeiro, Dawn, Matviychuk, Diana, Mercimek-Andrews, Saadet

Journal:

Year:

2019

Language:

english

File:

PDF, 1.00 MB

english, 2019

8

Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy

del CaÃ±o-Ochoa, Francisco, Ng, Bobby G., Abedalthagafi, Malak, Almannai, Mohammed, Cohn, Ronald D., Costain, Gregory, Elpeleg, Orly, Houlden, Henry, Karimiani, Ehsan Ghayoor, Liu, Pengfei, Manzini, M

Journal:

Genetics in Medicine

Year:

2020

File:

PDF, 803 KB

2020

9

Adult neuropsychiatric expression and familial segregation of 2q13 duplications

Costain, Gregory, Lionel, Anath C., Fu, Fiona, Stavropoulos, Dimitri J., Gazzellone, Matthew J., Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2014

Language:

english

File:

PDF, 188 KB

english, 2014

10

Reappraisal of Reported Genes for Sudden Arrhythmic Death: An Evidence-Based Evaluation of Gene Validity for Brugada Syndrome

Hosseini, S. Mohsen, Kim, Raymond, Udupa, Sharmila, Costain, Gregory, Jobling, Rebekah, Liston, Eriskay, Jamal, Seema M., Szybowska, Marta, Morel, Chantal F., Bowdin, Sarah, Garcia, John, Care, Melani

Journal:

Year:

2018

Language:

english

File:

PDF, 2.24 MB

english, 2018

11

Inflation Dynamics with Labour Market Matching: Assessing Alternative Specifications

Christoffel, Kai Philipp, Costain, James S., de Walque, Gregory, Kuester, Keith, Linzert, Tobias, Millard, Stephen, Pierrard, Olivier

Journal:

SSRN Electronic Journal

Year:

2009

Language:

english

File:

PDF, 547 KB

english, 2009

12

Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries

Costain, Gregory, Lionel, Anath C., Ogura, Lucas, Marshall, Christian R., Scherer, Stephen W., Silversides, Candice K., Bassett, Anne S.

Journal:

International Journal of Cardiology

Year:

2016

Language:

english

File:

PDF, 503 KB

english, 2016

13

Genomic Disorders in Psychiatry—What Does the Clinician Need to Know?

Lowther, Chelsea, Costain, Gregory, Baribeau, Danielle A., Bassett, Anne S.

Journal:

Current Psychiatry Reports

Year:

2017

Language:

english

File:

PDF, 1.11 MB

english, 2017

14

Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia

Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Waserman, Jack, Boyd, Kerry, Noor, Abdul, Speevak, Marsha, Stavropoulos, Dimitri J., Wei, John, Lionel, Anath C., Marshall, Christian R., Scherer,

Journal:

Genome Medicine

Year:

2017

Language:

english

File:

PDF, 598 KB

english, 2017

15

Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot

Reuter, Miriam S., Jobling, Rebekah, Chaturvedi, Rajiv R., Manshaei, Roozbeh, Costain, Gregory, Heung, Tracy, Curtis, Meredith, Hosseini, S. Mohsen, Liston, Eriskay, Lowther, Chelsea, Oechslin, Erwin,

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 497 KB

english, 2018

16

Absence of iron-responsive element-binding protein 2 causes a novel neurodegenerative syndrome

Costain, Gregory, Ghosh, Manik C, Maio, Nunziata, Carnevale, Amanda, Si, Yue C, Rouault, Tracey A, Yoon, Grace

Journal:

Year:

2019

Language:

english

File:

PDF, 1.02 MB

english, 2019

17

Practical guidelines for managing adults with 22q11.2 deletion syndrome

Fung, Wai Lun Alan, Butcher, Nancy J., Costain, Gregory, Andrade, Danielle M., Boot, Erik, Chow, Eva W.C., Chung, Brian, Cytrynbaum, Cheryl, Faghfoury, Hanna, Fishman, Leona, García-Miñaúr, Sixto, Geo

Journal:

Genetics in Medicine

Year:

2015

Language:

english

File:

PDF, 608 KB

english, 2015

18

Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome

Chan, Chrystal, Costain, Gregory, Ogura, Lucas, Silversides, Candice K., Chow, Eva W.C., Bassett, Anne S.

Journal:

Journal of Genetic Counseling

Year:

2015

Language:

english

File:

PDF, 333 KB

english, 2015

19

Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome

Van, Lily, Butcher, Nancy J., Costain, Gregory, Ogura, Lucas, Chow, Eva W. C., Bassett, Anne S.

Journal:

Genetics in Medicine

Year:

2015

Language:

english

File:

PDF, 609 KB

english, 2015

20

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature

Lowther, Chelsea, Costain, Gregory, Stavropoulos, Dimitri J., Melvin, Rebecca, Silversides, Candice K., Andrade, Danielle M., So, Joyce, Faghfoury, Hanna, Lionel, Anath C., Marshall, Christian R., Sch

Journal:

Genetics in Medicine

Year:

2015

Language:

english

File:

PDF, 483 KB

english, 2015

21

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

Bassett, Anne S., Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Chow, Eva W. C., van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van den Bree, Marianne, Murphy, K

Journal:

American Journal of Psychiatry

Year:

2017

Language:

english

File:

PDF, 587 KB

english, 2017

22

Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing

Costain, Gregory, Jobling, Rebekah, Walker, Susan, Reuter, Miriam S., Snell, Meaghan, Bowdin, Sarah, Cohn, Ronald D., Dupuis, Lucie, Hewson, Stacy, Mercimek-Andrews, Saadet, Shuman, Cheryl, Sondheimer

Journal:

European Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 434 KB

english, 2018

23

Precision Child Health: an Emerging Paradigm for Paediatric Quality and Safety

Costain, Gregory, Cohn, Ronald D., Malkin, David

Journal:

Current Treatment Options in Pediatrics

Year:

2020

File:

PDF, 256 KB

2020

24

Clinically detectable copy number variations in a Canadian catchment population of schizophrenia

Anne S. Bassett, Gregory Costain, Wai Lun Alan Fung, Kathryn J. Russell, Laura Pierce, Ronak Kapadia, Ronald F. Carter, Eva W.C. Chow, Pamela J. Forsythe

Journal:

Journal of Psychiatric Research

Year:

2010

Language:

english

File:

PDF, 137 KB

english, 2010

25

Reply: IREB2-associated neurodegeneration

Maio, Nunziata, Ghosh, Manik C, Costain, Gregory, Carnevale, Amanda, Si, Yue, Yoon, Grace, Rouault, Tracey A

Journal:

Year:

2019

Language:

english

File:

PDF, 439 KB

english, 2019

26

Challenges in Diagnosing Rare Genetic Causes of Common In Utero Presentations: Report of Two Patients with Mucolipidosis Type II (I-Cell Disease)

Costain, Gregory, Inbar-Feigenberg, Michal, Saleh, Maha, Yaniv-Salem, Shimrit, Ryan, Greg, Morgen, Eric, Goh, Elaine, Nishimura, Gen, Chitayat, David

Journal:

Journal of Pediatric Genetics

Year:

2018

Language:

english

File:

PDF, 170 KB

english, 2018

27

The importance of copy number variation in congenital heart disease

Costain, Gregory, Silversides, Candice K, Bassett, Anne S

Journal:

npj Genomic Medicine

Year:

2016

Language:

english

File:

PDF, 983 KB

english, 2016

28

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

Lionel, Anath C, Costain, Gregory, Monfared, Nasim, Walker, Susan, Reuter, Miriam S, Hosseini, S Mohsen, Thiruvahindrapuram, Bhooma, Merico, Daniele, Jobling, Rebekah, Nalpathamkalam, Thomas, Pellecch

Journal:

Genetics in Medicine

Year:

2017

Language:

english

File:

PDF, 219 KB

english, 2017

29

Adult expression of a 3q13.31 microdeletion

Lowther, Chelsea, Costain, Gregory, Melvin, Rebecca, Stavropoulos, Dimitri J, Lionel, Anath C, Marshall, Christian R, Scherer, Stephen W, Bassett, Anne S

Journal:

Molecular Cytogenetics

Year:

2014

Language:

english

File:

PDF, 346 KB

english, 2014

30

Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype

Costain, Gregory, Shugar, Andrea, Krishnan, Pradeep, Mahmutoglu, Saadet, Laughlin, Suzanne, Kannu, Peter

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 354 KB

english, 2017

31

Enzyme replacement therapy in perinatal hypophosphatasia: Case report of a negative outcome and lessons for clinical practice

Costain, Gregory, Moore, Aideen M., Munroe, Lauren, Williams, Alison, Zlotnik Shaul, Randi, Rockman-Greenberg, Cheryl, Offringa, Martin, Kannu, Peter

Journal:

Molecular Genetics and Metabolism Reports

Year:

2018

Language:

english

File:

PDF, 511 KB

english, 2018

32

The Ever-Evolving Concept of Clinical Significance and the Potential for Sins of Omission in Genetic Research

Costain, Gregory, Bassett, Anne S.

Journal:

American Journal of Bioethics

Year:

2012

Language:

english

File:

PDF, 83 KB

english, 2012

33

Chromosomal microarray analysis—a routine clinical genetic test for patients with schizophrenia

Baker, Kate, Costain, Gregory, Fung, Wai Lun Alan, Bassett, Anne S

Journal:

The Lancet Psychiatry

Year:

2014

Language:

english

File:

PDF, 185 KB

english, 2014

34

Functional outcomes of adults with 22q11.2 deletion syndrome

Butcher, Nancy J., Chow, Eva W.C., Costain, Gregory, Karas, Dominique, Ho, Andrew, Bassett, Anne S.

Journal:

Genetics in Medicine

Year:

2012

Language:

english

File:

PDF, 303 KB

english, 2012

35

De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome

Costain, Gregory, Callewaert, Bert, Gabriel, Heinz, Tan, Tiong Y., Walker, Susan, Christodoulou, John, Lazar, Tamas, Menten, Björn, Orkin, Julia, Sadedin, Simon, Snell, Meaghan, Vanlander, Arnaud, Ver

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 854 KB

english, 2018

36

MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome

Merico, Daniele, Costain, Gregory, Butcher, Nancy J., Warnica, William, Ogura, Lucas, Alfred, Simon E., Brzustowicz, Linda M., Bassett, Anne S.

Journal:

Frontiers in Neurology

Year:

2014

Language:

english

File:

PDF, 1.91 MB

english, 2014

37

Reproductive Genetic Testing and Human Genetic Variation in the Era of Genomic Medicine

Lowther, Chelsea, Costain, Gregory, Bassett, Anne S.

Journal:

American Journal of Bioethics

Year:

2015

Language:

english

File:

PDF, 46 KB

english, 2015

38

Concerns About the Heritability of Serious Mental Illness: A Not-So-Strange Interlude

Costain, Gregory

Journal:

American Journal of Psychiatry

Year:

2014

Language:

english

File:

PDF, 692 KB

english, 2014

39

13q13.1–q13.2 deletion in tetralogy of Fallot: Clinical report and a literature review

Gregory Costain, Candice K. Silversides, Christian R. Marshall, Mary Shago, Nicholas Costain, Anne S. Bassett

Journal:

International Journal of Cardiology

Year:

2011

Language:

english

File:

PDF, 657 KB

english, 2011

40

Parental expression is overvalued in the interpretation of rare inherited variants

Costain, Gregory

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 573 KB

english, 2015

41

Copy Number Variable MicroRNAs in Schizophrenia and Their Neurodevelopmental Gene Targets

Warnica, William, Merico, Daniele, Costain, Gregory, Alfred, Simon E., Wei, John, Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.

Journal:

Biological Psychiatry

Year:

2015

Language:

english

File:

PDF, 1.03 MB

english, 2015

42

Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways

Silversides, Candice K., Lionel, Anath C., Costain, Gregory, Merico, Daniele, Migita, Ohsuke, Liu, Ben, Yuen, Tracy, Rickaby, Jessica, Thiruvahindrapuram, Bhooma, Marshall, Christian R., Scherer, Step

Journal:

Year:

2012

Language:

english

File:

PDF, 389 KB

english, 2012

43

Incomplete Knowledge of the Clinical Context as a Barrier to Interpreting Incidental Genetic Research Findings

Costain, Gregory, Bassett, Anne S.

Journal:

American Journal of Bioethics

Year:

2013

Language:

english

File:

PDF, 109 KB

english, 2013

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски