Harripaul, R. : rechercher sur Z-Library

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1

Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from Pakistan

Sawal, H.A., Harripaul, R., Mikhailov, A., Dad, R., Ayub, M., Jawad Hassan, M., Vincent, J.B.

Journal:

Clinical Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 427 KB

english, 2016

2

Three Mutations in the Bilateral Frontoparietal Polymicrogyria Gene GPR56 in Pakistani Intellectual Disability Families

Sawal, Humaira, Harripaul, Ricardo, Mikhailov, Anna, Vleuten, Kayla, Naeem, Farooq, Nasr, Tanveer, Hassan, Muhammad, Vincent, John, Ayub, Muhammad, Rafiq, Muhammad

Journal:

Journal of Pediatric Genetics

Année:

2018

Langue:

english

Fichier:

PDF, 352 KB

english, 2018

3

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

Harripaul, R, Vasli, N, Mikhailov, A, Rafiq, M A, Mittal, K, Windpassinger, C, Sheikh, T I, Noor, A, Mahmood, H, Downey, S, Johnson, M, Vleuten, K, Bell, L, Ilyas, M, Khan, F S, Khan, V, Moradi, M, Ay

Journal:

Molecular Psychiatry

Année:

2017

Langue:

english

Fichier:

PDF, 2.77 MB

english, 2017

4

Towards precision medicine in generalized anxiety disorder: review of genetics and pharmaco(epi)genetics

Tomasi, Julia, Lisoway, Amanda J., Zai, Clement C., Harripaul, Ricardo, Müller, Daniel J., Zai, Gwyneth C.M., McCabe, Randi E., Richter, Margaret A., Kennedy, James L., Tiwari, Arun K.

Journal:

Journal of Psychiatric Research

Année:

2019

Langue:

english

Fichier:

PDF, 789 KB

english, 2019

5

Coping with Student Teacher Stress at the University of Trinidad and Tobago

Gowrie, George, Ramdass, Mala, Singh, Vashti, Birbal, Roland, Harripaul, Cyril, Hosein, Shaheeda

Journal:

International Research in Higher Education

Année:

2015

Langue:

english

Fichier:

PDF, 191 KB

english, 2015

6

Antidepressant-Associated Mania in Bipolar Disorder

Melhuish Beaupre, Lindsay M., Tiwari, Arun K., GonÃ§alves, Vanessa F., Lisoway, Amanda J., Harripaul, Ricardo S., MÃ¼ller, Daniel J., Zai, Clement C., Kennedy, James L.

Journal:

Journal of Clinical Psychopharmacology

Année:

2020

Fichier:

PDF, 173 KB

2020

7

Prediction of physical violence in schizophrenia with machine learning algorithms

Wang, Kevin Z., Bani-Fatemi, Ali, Adanty, Christopher, Harripaul, Ricardo, Griffiths, John, Kolla, Nathan, Gerretsen, Philip, Graff, Ariel, De Luca, Vincenzo

Journal:

Psychiatry Research

Année:

2020

Fichier:

PDF, 849 KB

2020

8

The Effect of Transforming Care at the Bedside Initiative on Healthcare Teams’ Work Environments

Lavoie-Tremblay, Mélanie, O'Conner, Patricia, Harripaul, Anastasia, Biron, Alain, Ritchie, Judith, Lavigne, Genevieve L., Baillargeon, Sophie, Ringer, Justin, MacGibbon, Brenda, Taylor-Ducharme, Sharo

Journal:

Worldviews on Evidence-Based Nursing

Année:

2014

Langue:

english

Fichier:

PDF, 159 KB

english, 2014

9

Care Transitions

Dusek, Brenda, Pearce, Nancy, Harripaul, Anastasia, Lloyd, Monique

Journal:

Journal of Nursing Care Quality

Année:

2015

Langue:

english

Fichier:

PDF, 97 KB

english, 2015

10

Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability

Mittal, Kirti, Rafiq, Muhammad A, Rafiullah, Rafiullah, Harripaul, Ricardo, Ali, Hazrat, Ayaz, Muhammad, Aslam, Muhammad, Naeem, Farooq, Amin-ud-din, Muhammad, Waqas, Ahmed, So, Joyce, Rappold, Gudrun

Journal:

Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 940 KB

english, 2016

11

CE

Lavoie-Tremblay, Melanie, OʼConnor, Patricia, Harripaul, Anastasia, Biron, Alain, Ritchie, Judith, MacGibbon, Brenda, Cyr, Guylaine

Journal:

AJN American Journal of Nursing

Année:

2014

Langue:

english

Fichier:

PDF, 570 KB

english, 2014

12

Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

Johansen, Anide, Rosti, Rasim O., Musaev, Damir, Sticca, Evan, Harripaul, Ricardo, Zaki, Maha, Çağlayan, Ahmet Okay, Azam, Matloob, Sultan, Tipu, Froukh, Tawfiq, Reis, André, Popp, Bernt, Ahmed, Iltaf

Journal:

The American Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 639 KB

english, 2016

13

The Use of Next-Generation Sequencing for Research and Diagnostics for Intellectual Disability

Harripaul, Ricardo, Noor, Abdul, Ayub, Muhammad, Vincent, John B.

Journal:

Cold Spring Harbor Perspectives in Medicine

Année:

2017

Langue:

english

Fichier:

PDF, 568 KB

english, 2017

14

231. Serotonin Transporter Gene Methylation and Antidepressant Treatment of Major Depressive Disorder

Lisoway, Amanda, Zai, Clement C., Tiwari, Arun K., Harripaul, Ricardo, Freeman, Natalie, Oh, Gabriel, French, Leon, Kaminsky, Zachary A., Kennedy, James

Journal:

Biological Psychiatry

Année:

2017

Langue:

english

Fichier:

PDF, 42 KB

english, 2017

15

Investigating The Role of Treatable Genetic Diseases In Schizophrenia And Bipolar Disorder Populations And Its Clinical Diagnostic Impact

Zai, Clement, Sriretnakumar, Venuja, Harripaul, Ricardo, Mittal, Kirti, Kennedy, James L., So, Joyce

Journal:

European Neuropsychopharmacology

Année:

2017

Langue:

english

Fichier:

PDF, 35 KB

english, 2017

16

MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro

Sheikh, Taimoor I., Harripaul, Ricardo, Ayub, Muhammad, Vincent, John B.

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 2.13 MB

english, 2018

17

Seventy Years of RN Effectiveness: A Database Development Project to Inform Best Practice

Lulat, Zainab, Blain-McLeod, Julie, Grinspun, Doris, Penney, Tasha, Harripaul-Yhap, Anastasia, Rey, Michelle

Journal:

Worldviews on Evidence-Based Nursing

Année:

2018

Langue:

english

Fichier:

PDF, 613 KB

english, 2018

18

Biallelic missense variants in ZBTB11 can cause intellectual disability in human

Fattahi, Zohreh, Sheikh, Taimoor I, Musante, Luciana, Rasheed, Memoona, Taskiran, Ibrahim Ihsan, Harripaul, Ricardo, Hu, Hao, Kazeminasab, Somayeh, Alam, Muhammad Rizwan, Hosseini, Masoumeh, Larti, Fa

Journal:

Human Molecular Genetics

Année:

2018

Langue:

english

Fichier:

PDF, 910 KB

english, 2018

19

SA94. When Rare Meets Common: Burden and Impact of Treatable Rare Genetic Diseases in Primary Psychiatric Populations

Sriretnakumar, Venuja, Harripaul, Ricardo, Mittal, Kirti, Kennedy, James, So, Joyce

Journal:

Schizophrenia Bulletin

Année:

2017

Langue:

english

Fichier:

PDF, 71 KB

english, 2017

20

F195. ENRICHMENT OF PATHOGENIC VARIANTS ASSOCIATED WITH TREATABLE GENETIC DISEASES IN LARGE SCHIZOPHRENIA, BIPOLAR AND DEPRESSION COHORTS

Sriretnakumar, Venuja, Harripaul, Ricardo, Vincent, John, Kennedy, James, So, Joyce

Journal:

Schizophrenia Bulletin

Année:

2018

Langue:

english

Fichier:

PDF, 98 KB

english, 2018

21

Enrichment of pathogenic variants in genes associated with inborn errors of metabolism in psychiatric populations

Sriretnakumar, Venuja, Harripaul, Ricardo, Vincent, John B., Kennedy, James L., So, Joyce

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2018

Langue:

english

Fichier:

PDF, 1.25 MB

english, 2018

22

Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations

Gul, Hadia, Shah, Abdul Haleem, Harripaul, Ricardo, Mikhailov, Anna, Prajapati, Kamalben, Khan, Ejazullah, Ullah, Farman, Zubair, Muhammad, Ali, Muhammad Zeeshan, Shah, Ayesha Haleem, Salman, Said, Kh

Journal:

Annals of Human Genetics

Année:

2019

Fichier:

PDF, 694 KB

2019

23

WHOLE EXOME TRIO SEQUENCING IDENTIFIES NOVEL VARIANTS FOR AUTISM SPECTRUM DISORDER

Harripaul, Ricardo, Vasli, Nasim, Rodrigues, Ashlyn, Rabia, Ansa, Mahmood, Saqib, Heidari, Abolfazl, Al Ayadhi, Laila, Bozorgmehr, Bita, Sasanfar, Roksana, Ayub, Muhammad, Vincent, John

Journal:

European Neuropsychopharmacology

Année:

2019

Langue:

english

Fichier:

PDF, 44 KB

english, 2019

24

INCREASED FREQUENCY OF RARE GENETIC DISEASE VARIANTS IN LARGE SCHIZOPHRENIA, BIPOLAR, AND DEPRESSION POPULATIONS

Sriretnakumar, Venuja, Harripaul, Ricardo, Mittal, Kirti, Vincent, John B., Kennedy, James L., So, Joyce

Journal:

European Neuropsychopharmacology

Année:

2019

Langue:

english

Fichier:

PDF, 35 KB

english, 2019

25

GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates

Ouyang, Qing, Kavanaugh, Brian C., Joesch-Cohen, Lena, Dubois, Bethany, Wu, Qing, Schmidt, Michael, Baytas, Ozan, Pastore, Stephen F., Harripaul, Ricardo, Mishra, Sasmita, Hussain, Abrar, Kim, Katheri

Journal:

Année:

2019

Langue:

english

Fichier:

PDF, 7.48 MB

english, 2019

26

Towards precision medicine in generalized anxiety disorder: review of genetics and pharmaco(epi)genetics

Tomasi, Julia, Lisoway, Amanda J., Zai, Clement C., Harripaul, Ricardo, Müller, Daniel J., Zai, Gwyneth C.M., McCabe, Randi E., Richter, Margaret A., Kennedy, James L., Tiwari, Arun K.

Journal:

Journal of Psychiatric Research

Année:

2019

Fichier:

PDF, 789 KB

2019

27

Coping with Student Teacher Stress at the University of Trinidad and Tobago

Gowrie, George, Ramdass, Mala, Singh, Vashti, Birbal, Roland, Harripaul, Cyril, Hosein, Shaheeda

Journal:

International Research in Higher Education

Année:

2015

Fichier:

PDF, 191 KB

2015

28

A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain

Pastore, Stephen, Harripaul, Ricardo, Azam, Matloob, Vincent, John B.

Journal:

Journal of Human Genetics

Année:

2020

Fichier:

PDF, 1.12 MB

2020

29

Unexplained weight loss in an 80-year-old woman

Taylor, I. A., Gill, I., Harripaul, A.

Journal:

Année:

2015

Fichier:

PDF, 226 KB

2015