Scerri, Thomas S: search on Z-Library

Fundraising September 15, 2024 – October 1, 2024 About fundraising

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

Fundraising September 15, 2024 – October 1, 2024

Z-Library is one of the largest online libraries in the world that contains over 17,000,000 books and 84,837,000 articles. We aim to make literature accessible to everyone. Today (September 15, 2024) we've started additional fundraising to project maintenance and development.

Also UNLIMITED downloads (for 31 days after the day of making donation) are available for ALL contributors who will donate during the fundraising period till October 1, 2024.

About fundraisingRead more

Make a donation

1

Did Our Species Evolve in Subdivided Populations across Africa, and Why Does It Matter?

Scerri, Eleanor M.L., Thomas, Mark G., Manica, Andrea, Gunz, Philipp, Stock, Jay T., Stringer, Chris, Grove, Matt, Groucutt, Huw S., Timmermann, Axel, Rightmire, G. Philip, d’Errico, Francesco, Tryon,

Journal:

Trends in Ecology & Evolution

Year:

2018

Language:

english

File:

PDF, 3.06 MB

english, 2018

2

Beyond multiregional and simple out-of-Africa models of human evolution

Scerri, Eleanor M. L., Chikhi, Lounès, Thomas, Mark G.

Journal:

Nature Ecology & Evolution

Year:

2019

File:

PDF, 899 KB

2019

3

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

Eising, Else, Carrion-Castillo, Amaia, Vino, Arianna, Strand, Edythe A., Jakielski, Kathy J., Scerri, Thomas S., Hildebrand, Michael S., Webster, Richard, Ma, Alan, Mazoyer, Bernard, Francks, Clyde, B

Journal:

Molecular Psychiatry

Year:

2018

Language:

english

File:

PDF, 1.92 MB

english, 2018

4

Genetics of developmental dyslexia

Thomas S. Scerri, Gerd Schulte-Körne

Journal:

European Child & Adolescent Psychiatry

Year:

2010

Language:

english

File:

PDF, 611 KB

english, 2010

5

Familial juvenile systemic granulomatosis (Blau's syndrome)

L. SCERRI, L.J. COOK, E.A. JENKINS, A.L. THOMAS

Journal:

Clinical and Experimental Dermatology

Year:

1996

Language:

english

File:

PDF, 2.06 MB

english, 1996

6

Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

Alistair T. Pagnamenta, Elena Bacchelli, Maretha V. de Jonge, Ghazala Mirza, Thomas S. Scerri, Fiorella Minopoli, Andreas Chiocchetti, Kerstin U. Ludwig, Per Hoffmann, Silvia Paracchini, Ernesto Lowy,

Journal:

Biological Psychiatry

Year:

2010

Language:

english

File:

PDF, 948 KB

english, 2010

7

An α-E-catenin ( CTNNA1 ) mutation in hereditary diffuse gastric cancer

Majewski, Ian J, Kluijt, Irma, Cats, Annemieke, Scerri, Thomas S, de Jong, Daphne, Kluin, Roelof JC, Hansford, Samantha, Hogervorst, Frans BL, Bosma, Astrid J, Hofland, Ingrid, Winter, Marcel, Huntsma

Journal:

The Journal of Pathology

Year:

2013

Language:

english

File:

PDF, 334 KB

english, 2013

8

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

Simpson, Nuala H, Addis, Laura, Brandler, William M, Slonims, Vicky, Clark, Ann, Watson, Jocelynne, Scerri, Thomas S, Hennessy, Elizabeth R, Bolton, Patrick F, Conti-Ramsden, Gina, Fairfax, Benjamin P

Journal:

Developmental Medicine & Child Neurology

Year:

2014

Language:

english

File:

PDF, 385 KB

english, 2014

9

The Genetic Lexicon of Dyslexia

Paracchini, Silvia, Scerri, Thomas, Monaco, Anthony P.

Journal:

Annual Review of Genomics and Human Genetics

Year:

2007

Language:

english

File:

PDF, 561 KB

english, 2007

10

A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene

Dennis, Megan Y., Paracchini, Silvia, Scerri, Thomas S., Prokunina-Olsson, Ludmila, Knight, Julian C., Wade-Martins, Richard, Coggill, Penny, Beck, Stephan, Green, Eric D., Monaco, Anthony P., Stubbs,

Journal:

Year:

2009

Language:

english

File:

PDF, 731 KB

english, 2009

11

Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill

Brandler, William M., Morris, Andrew P., Evans, David M., Scerri, Thomas S., Kemp, John P., Timpson, Nicholas J., St Pourcain, Beate, Smith, George Davey, Ring, Susan M., Stein, John, Monaco, Anthony

Journal:

Year:

2013

Language:

english

File:

PDF, 412 KB

english, 2013

12

Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency

Fliegauf, Manfred, L. Bryant, Vanessa, Frede, Natalie, Slade, Charlotte, Woon, See-Tarn, Lehnert, Klaus, Winzer, Sandra, Bulashevska, Alla, Scerri, Thomas, Leung, Euphemia, Jordan, Anthony, Keller, Ba

Journal:

The American Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 2.11 MB

english, 2015

13

Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population

Paracchini, Silvia, Steer, Colin D., Buckingham, Lyn-Louise, Morris, Andrew P., Ring, Susan, Scerri, Thomas, Stein, John, Pembrey, Marcus E., Ragoussis, Jiannis, Golding, Jean, Monaco, Anthony P.

Journal:

American Journal of Psychiatry

Year:

2008

Language:

english

File:

PDF, 177 KB

english, 2008

14

Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5

Scerri, Thomas, Riseley, Jessica R., Gillies, Greta, Pope, Kate, Burgess, Rosemary, Mandelstam, Simone A., Dibbens, Leanne, Chow, Chung W., Maixner, Wirginia, Harvey, Anthony Simon, Jackson, Graeme D.

Journal:

Annals of Clinical and Translational Neurology

Year:

2015

Language:

english

File:

PDF, 286 KB

english, 2015

15

Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3

Sim, Joe C., Scerri, Thomas, Fanjul-Fernández, Miriam, Riseley, Jessica R., Gillies, Greta, Pope, Kate, van Roozendaal, Hanna, Heng, Julian I., Mandelstam, Simone A., McGillivray, George, MacGregor, D

Journal:

Annals of Neurology

Year:

2016

Language:

english

File:

PDF, 561 KB

english, 2016

16

Genome-wide analyses identify common variants associated with macular telangiectasia type 2

Scerri, Thomas S, Quaglieri, Anna, Cai, Carolyn, Zernant, Jana, Matsunami, Nori, Baird, Lisa, Scheppke, Lea, Bonelli, Roberto, Yannuzzi, Lawrence A, Friedlander, Martin, Egan, Catherine A, Fruttiger,

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 1.28 MB

english, 2017

17

Primary immunodeficiencies of the NF-kappaB pathway

Slade, Charlotte A., Tempany, Jessica, Fliegauf, Manfred, Woon, See-Tarn, Scerri, Thomas, Leung, Euphemia, Ameratunga, Rohan V., van der Meer, Jos W.M., Douglass, Jo, Grimbacher, Bodo, Hodgkin, Philip

Journal:

Year:

2017

Language:

english

File:

PDF, 58 KB

english, 2017

18

Investigating the role of somatic mutations in malformations of brain development

Leventer, Richard J., Scerri, Thomas, Marsh, Ashley P.L., Maixner, Wirginia, MacGregor, Duncan, Harvey, A. Simon, Delatycki, Martin B., Amor, David J., Bahlo, Melanie, Lockhart, Paul J.

Journal:

Year:

2017

Language:

english

File:

PDF, 43 KB

english, 2017

19

CIP2A expression predicts recurrences of tamoxifen-treated breast cancer

Baldacchino, Shawn, Wastall, Laura M, Saliba, Christian, Hughes, Thomas A, Scerri, Christian, Berwick, Angelene, Speirs, Valerie, Hanby, Andrew M, Grech, Godfrey

Journal:

Year:

2017

Language:

english

File:

PDF, 822 KB

english, 2017

20

Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

de Vos, Ivo J H M, Tao, Evelyn Yaqiong, Ong, Sheena Li Ming, Goggi, Julian L, Scerri, Thomas, Wilson, Gabrielle R, Low, Chernis Guai Mun, Wong, Arnette Shi Wei, Grussu, Dominic, Stegmann, Alexander P

Journal:

Human Molecular Genetics

Year:

2018

Language:

english

File:

PDF, 1.08 MB

english, 2018

21

Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18

Scerri, Thomas S., Paracchini, Silvia, Morris, Andrew, MacPhie, I. Laurence, Talcott, Joel, Stein, John, Smith, Shelley D., Pennington, Bruce F., Olson, Richard K., DeFries, John C., Monaco, Anthony P

Journal:

Year:

2010

Language:

english

File:

PDF, 353 KB

english, 2010

22

Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2

Slade, Charlotte A., McLean, Catriona, Scerri, Thomas, Giang, Tran Binh, Megaloudis, Steven, Strathmore, Alexander, Tempany, Jessica C., Nicholls, Katherine, D’Arcy, Colleen, Bahlo, Melanie, Hodgkin,

Journal:

Journal of Clinical Immunology

Year:

2019

Language:

english

File:

PDF, 8.74 MB

english, 2019

23

Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia

Khan, Kamal, Zech, Michael, Morgan, Angela T., Amor, David J., Skorvanek, Matej, Khan, Tahir N., Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Coleman, Matthew, Rigbye, Kristin A.,

Journal:

Genetics in Medicine

Year:

2019

Language:

english

File:

PDF, 1.46 MB

english, 2019

24

Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia

Khan, Kamal, Zech, Michael, Morgan, Angela T., Amor, David J., Skorvanek, Matej, Khan, Tahir N., Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Coleman, Matthew, Rigbye, Kristin A.,

Journal:

Genetics in Medicine

Year:

2019

File:

PDF, 1.46 MB

2019

25

Severe childhood speech disorder

Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Van Reyk, Olivia, Coleman, Matthew, Braden, Ruth O., Turner, Samantha, Rigbye, Kristin A., Boys, Amber, Barton, Sarah, Webster, Richard

Journal:

Year:

2020

File:

PDF, 2.55 MB

2020