Fadi Hamdan: search on Z-Library

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1

Association between mobile phone use and neck pain in university students: A cross-sectional study using numeric rating scale for evaluation of neck pain

Al-Hadidi, Fadi, Bsisu, Isam, AlRyalat, Saif Aldeen, Al-Zu’bi, Belal, Bsisu, Rasha, Hamdan, Mohammad, Kanaan, Tareq, Yasin, Mohamad, Samarah, Omar, Kamolz, Lars-Peter

Journal:

Year:

2019

Language:

english

File:

PDF, 748 KB

english, 2019

2

Intensive and extensive disaster risk drivers and interactions with recent trends in the global political economy, with special emphasis on rentier states

Journal:

International Journal of Disaster Risk Reduction

Year:

2014

Language:

english

File:

PDF, 724 KB

english, 2014

3

De Novo Mutations in Moderate or Severe Intellectual Disability

Hamdan, Fadi F., Srour, Myriam, Capo-Chichi, Jose-Mario, Daoud, Hussein, Nassif, Christina, Patry, Lysanne, Massicotte, Christine, Ambalavanan, Amirthagowri, Spiegelman, Dan, Diallo, Ousmane, Henrion,

Journal:

Year:

2014

Language:

english

File:

PDF, 557 KB

english, 2014

4

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

Julie Gauthier, Tabrez J. Siddiqui, Peng Huashan, Daisaku Yokomaku, Fadi F. Hamdan, Nathalie Champagne, Mathieu Lapointe, Dan Spiegelman, Anne Noreau, Ronald G. Lafrenière, Ferid Fathalli, Ridha Joobe

Journal:

Year:

2011

Language:

english

File:

PDF, 2.21 MB

english, 2011

5

SHANK1 Deletions in Males with Autism Spectrum Disorder

Daisuke Sato, Anath C. Lionel, Claire S. Leblond, Aparna Prasad, Dalila Pinto, Susan Walker, Irene O'Connor, Carolyn Russell, Irene E. Drmic, Fadi F. Hamdan, Jacques L. Michaud, Volker Endris, Ralph R

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 303 KB

english, 2012

6

PERIOPERATIVE USE OF PREGABALIN IN TOTAL KNEE ARTHROPLASTY: META-ANALYSIS OF RANDOMIZED CONTROLLED TRIALS

Tayyem, Mohammed, Elhadid, Fadi, Haddad, Ra’d, Samarah, Omar, Ananzah, Mohammed, Ahmad, Mohammad, Hamdan, Mohammad

Journal:

Journal of Musculoskeletal Research

Year:

2017

Language:

english

File:

PDF, 384 KB

english, 2017

7

De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism

Fadi F. Hamdan, Hussein Daoud, Amélie Piton, Julie Gauthier, Sylvia Dobrzeniecka, Marie-Odile Krebs, Ridha Joober, Jean-Claude Lacaille, Amélie Nadeau, Jeff M. Milunsky, Zhenyuan Wang, Lionel Carmant,

Journal:

Biological Psychiatry

Year:

2011

Language:

english

File:

PDF, 355 KB

english, 2011

8

De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

Fadi F. Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie-Odile Krebs, Ridha Joober, Ronald G. Lafrenière, Jean-Claude L

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 670 KB

english, 2010

9

Mutations in DOCK7 in Individuals with Epileptic Encephalopathy and Cortical Blindness

Perrault, Isabelle, Hamdan, Fadi F., Rio, Marlène, Capo-Chichi, José-Mario, Boddaert, Nathalie, Décarie, Jean-Claude, Maranda, Bruno, Nabbout, Rima, Sylvain, Michel, Lortie, Anne, Roux, Philippe P., R

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.32 MB

english, 2014

10

Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability

Fadi F. Hamdan, Julie Gauthier, Yoichi Araki, Da-Ting Lin, Yuhki Yoshizawa, Kyohei Higashi, A-Reum Park, Dan Spiegelman, Sylvia Dobrzeniecka, Amélie Piton, Hideyuki Tomitori, Hussein Daoud, Christine

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 981 KB

english, 2011

11

Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population

Myriam Srour, Jeremy Schwartzentruber, Fadi F. Hamdan, Luis H. Ospina, Lysanne Patry, Damian Labuda, Christine Massicotte, Sylvia Dobrzeniecka, José-Mario Capo-Chichi, Simon Papillon-Cavanagh, Mark E.

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 531 KB

english, 2012

12

A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review

Merner, Nancy, Forgeot d'Arc, Baudouin, Bell, Scott C., Maussion, Gilles, Peng, Huashan, Gauthier, Julie, Crapper, Liam, Hamdan, Fadi F., Michaud, Jacques L., Mottron, Laurent, Rouleau, Guy A., Ernst,

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 399 KB

english, 2016

13

HeterozygousHNRNPUvariants cause early onset epilepsy and severe intellectual disability

Bramswig, Nuria C., Lüdecke, Hermann-Josef, Hamdan, Fadi F., Altmüller, Janine, Beleggia, Filippo, Elcioglu, Nursel H., Freyer, Catharine, Gerkes, Erica H., Demirkol, Yasemin Kendir, Knupp, Kelly G.,

Journal:

Year:

2017

Language:

english

File:

PDF, 798 KB

english, 2017

14

Variant analysis of the first Lebanese SARS-CoV-2 isolates

Abou-Hamdan, Mhamad, Hamze, Kassem, Sater, Ali Abdel, Akl, Haidar, El-zein, Nabil, Dandache, Israa, Abdel-sater, Fadi

Journal:

Year:

2020

File:

PDF, 34 KB

2020

15

OCCIPITAL BLOCKADE FOR POSTDURAL PUNCTURE HEADACHE: DO WE HARM?

Ahed Zeidan, Fadi Hamdan

Journal:

Year:

2009

Language:

english

File:

PDF, 30 KB

english, 2009

16

Use of an in Situ Disulfide Cross-Linking Strategy To Study the Dynamic Properties of the Cytoplasmic End of Transmembrane Domain VI of the M 3 Muscarinic Acetylcholine Receptor †

Ward, Stuart D. C., Hamdan, Fadi F., Bloodworth, Lanh M., Siddiqui, Nasir A., Li, Jian Hua, Wess, Jürgen

Journal:

Year:

2006

Language:

english

File:

PDF, 427 KB

english, 2006

17

De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive Impairment, Spastic Paraparesis, Axonal Neuropathy, and Cerebellar Atrophy

Lee, Jae-Ran, Srour, Myriam, Kim, Doyoun, Hamdan, Fadi. F., Lim, So-Hee, Brunel-Guitton, Catherine, Décarie, Jean-Claude, Rossignol, Elsa, Mitchell, Grant A., Schreiber, Allison, Moran, Rocio, Van Har

Journal:

Year:

2015

Language:

english

File:

PDF, 1.55 MB

english, 2015

18

Use of magnetic resonance imaging to determine laterality of meniscal size in healthy volunteers

Hamdan, Mohammad, Haddad, Bassem, Isleem, Ula, Yaghi, Rami, Bani Hamad, Salsabiela, Al-Balkhi, Rahaf, Afifi, Rami, Alryalat, Saif Aldeen, Hadidi, Fadi, Khanfar, Aws, Shatarat, Amjad, Erickson, Brandon

Journal:

Year:

2020

File:

PDF, 712 KB

2020

19

A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome

Gauthier, Julie, Ouled Amar Bencheikh, Bouchra, Hamdan, Fadi F, Harrison, Steven M, Baker, Linda A, Couture, Françoise, Thiffault, Isabelle, Ouazzani, Reda, Samuels, Mark E, Mitchell, Grant A, Rouleau

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 485 KB

english, 2015

20

Late-presenting developmental dysplasia of the hip in Jordanian males. A retrospective hospital based study

Samarah, Omar, Al Hadidi, Fadi, Hamdan, Mohammad, Hantouly, Ashraf

Journal:

Saudi Medical Journal

Year:

2016

File:

PDF, 337 KB

2016

21

Cloning of the chaperonin t-complex polypeptide 1 gene fromSchistosoma mansoniand studies of its expression levels under heat shock and oxidative stress

Élida G. Campos, Fadi F. Hamdan

Journal:

Parasitology Research

Year:

2000

Language:

english

File:

PDF, 284 KB

english, 2000

22

Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts

Philip Awadalla, Julie Gauthier, Rachel A. Myers, Ferran Casals, Fadi F. Hamdan, Alexander R. Griffing, Mélanie Côté, Edouard Henrion, Dan Spiegelman, Julien Tarabeux, Amélie Piton, Yan Yang, Adam Boy

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 134 KB

english, 2010

23

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

Cappello, Silvia, Gray, Mary J, Badouel, Caroline, Lange, Simona, Einsiedler, Melanie, Srour, Myriam, Chitayat, David, Hamdan, Fadi F, Jenkins, Zandra A, Morgan, Tim, Preitner, Nadia, Uster, Tami, Tho

Journal:

Nature Genetics

Year:

2013

Language:

english

File:

PDF, 2.18 MB

english, 2013

24

Functional expression of M1, M3 and M5 muscarinic acetylcholine receptors in yeast

Isolde Erlenbach, Evi Kostenis, Clarice Schmidt, Fadi F. Hamdan, Mark H. Pausch, Jürgen Wess

Journal:

Journal of Neurochemistry

Year:

2001

Language:

english

File:

PDF, 773 KB

english, 2001

25

Modelling of unbounded media for fluid-structure interaction applications - a review

Journal:

Year:

1998

Language:

english

File:

PDF, 999 KB

english, 1998

26

Identification and Biochemical Characterization of a Novel Mutation in DDX11 Causing Warsaw Breakage Syndrome

Capo-Chichi, José-Mario, Bharti, Sanjay Kumar, Sommers, Joshua A., Yammine, Tony, Chouery, Eliane, Patry, Lysanne, Rouleau, Guy A., Samuels, Mark E., Hamdan, Fadi F., Michaud, Jacques L., Brosh Jr, Ro

Journal:

Year:

2013

Language:

english

File:

PDF, 339 KB

english, 2013

27

Ligand-Specific Changes in M 3 Muscarinic Acetylcholine Receptor Structure Detected by a Disulfide Scanning Strategy †

Li, Jian Hua, Hamdan, Fadi F., Kim, Soo-Kyung, Jacobson, Kenneth A., Zhang, Xiaohong, Han, Sung-Jun, Wess, Jürgen

Journal:

Year:

2008

Language:

english

File:

PDF, 1.82 MB

english, 2008

28

Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophy

Hamdan, Fadi F, Saitsu, Hirotomo, Nishiyama, Kiyomi, Gauthier, Julie, Dobrzeniecka, Sylvia, Spiegelman, Dan, Lacaille, Jean-Claude, Décarie, Jean-Claude, Matsumoto, Naomichi, Rouleau, Guy A, Michaud,

Journal:

European Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 428 KB

english, 2012

29

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

Hamdan, Fadi F., Myers, Candace T., Cossette, Patrick, Lemay, Philippe, Spiegelman, Dan, Laporte, Alexandre Dionne, Nassif, Christina, Diallo, Ousmane, Monlong, Jean, Cadieux-Dion, Maxime, Dobrzenieck

Journal:

The American Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 922 KB

english, 2017

30

Validation of the Arabic version of the Kujala patellofemoral pain scoring system

Hamdan, Mohammad, Haddad, Bassem, Isleem, Ula, Hamad, Anas, Hussein, Lutfi, Shawareb, Yanal, Hadidi, Fadi, Alryalat, Saif Aldeen, Samarah, Omar, Khanfar, Aws, Alzoubi, Belal

Journal:

Journal of Orthopaedic Science

Year:

2018

Language:

english

File:

PDF, 211 KB

english, 2018

31

Metabolic Roles of the M 3 Muscarinic Acetylcholine Receptor Studied with M 3 Receptor Mutant Mice: A Review

GAUTAM, DINESH, JEON, JONGRYE, LI, JIAN HUA, HAN, SUNG-JUN, HAMDAN, FADI F., CUI, YINGHONG, LU, HUIYAN, DENG, CHUXIA, GAVRILOVA, OKSANA, WESS, JÜRGEN

Journal:

Journal of Receptor and Signal Transduction Research

Year:

2008

Language:

english

File:

PDF, 1.19 MB

english, 2008

32

De novo mutations in the gene encoding the synaptic scaffolding proteinSHANK3in patients ascertained for schizophrenia

Julie Gauthier, Nathalie Champagne, Ronald G. Lafrenière, Lan Xiong, Dan Spiegelman, Edna Brustein, Mathieu Lapointe, Huashan Peng, Mélanie Côté, Anne Noreau, Fadi F. Hamdan, Anjené M. Addington, Judi

Journal:

Proceedings of the National Academy of Sciences

Year:

2010

Language:

english

File:

PDF, 1.54 MB

english, 2010

33

Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness

Hamdan, Fadi F., Perrault, Isabelle, Rio, Marlène, Capo-Chichi, José-Mario, Boddaert, Nathalie, Décarie, Jean-Claude, Maranda, Bruno, Nabbout, Rima, Sylvain, Michel, Lortie, Anne, Roux, Philippe P., R

Journal:

International Journal of Developmental Neuroscience

Year:

2015

Language:

english

File:

PDF, 84 KB

english, 2015

34

Intellectual disability without epilepsy associated with STXBP1 disruption

Hamdan, Fadi F, Gauthier, Julie, Dobrzeniecka, Sylvia, Lortie, Anne, Mottron, Laurent, Vanasse, Michel, D'Anjou, Guy, Lacaille, Jean Claude, Rouleau, Guy A, Michaud, Jacques L

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 211 KB

english, 2011

35

Novel de novo SHANK3 mutation in autistic patients

Julie Gauthier, Dan Spiegelman, Amélie Piton, Ronald G. Lafrenière, Sandra Laurent, Judith St-Onge, Line Lapointe, Fadi F. Hamdan, Patrick Cossette, Laurent Mottron, Éric Fombonne, Ridha Joober, Claud

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2009

Language:

english

File:

PDF, 207 KB

english, 2009

36

Cloning and sequence analysis of a lysophospholipase homologue fromSchistosoma mansoni

Fadi F. Hamdan, Paula Ribeiro

Journal:

Parasitology Research

Year:

1998

Language:

english

File:

PDF, 419 KB

english, 1998

37

A critical role for β cell M3 muscarinic acetylcholine receptors in regulating insulin release and blood glucose homeostasis in vivo

Dinesh Gautam, Sung-Jun Han, Fadi F. Hamdan, Jongrye Jeon, Bo Li, Jian Hua Li, Yinghong Cui, David Mears, Huiyan Lu, Chuxia Deng, Thomas Heard, Jürgen Wess

Journal:

Cell Metabolism

Year:

2006

Language:

english

File:

PDF, 466 KB

english, 2006

38

Neuroblastoma Amplified Sequence (NBAS) mutation in recurrent acute liver failure: Confirmatory report in a sibship with very early onset, osteoporosis and developmental delay

Capo-Chichi, José-Mario, Mehawej, Cybel, Delague, Valerie, Caillaud, Catherine, Khneisser, Issam, Hamdan, Fadi F., Michaud, Jacques L., Kibar, Zoha, Mégarbané, André

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 380 KB

english, 2015

39

A novel homozygous AP4B1 mutation in two brothers with AP-4 deficiency syndrome and ocular anomalies

Accogli, Andrea, Hamdan, Fadi F., Poulin, Chantal, Nassif, Christina, Rouleau, Guy A., Michaud, Jacques L., Srour, Myriam

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 477 KB

english, 2018

40

Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes

Tucker, Tracy, Zahir, Farah R, Griffith, Malachi, Delaney, Allen, Chai, David, Tsang, Erica, Lemyre, Emmanuelle, Dobrzeniecka, Sylvia, Marra, Marco, Eydoux, Patrice, Langlois, Sylvie, Hamdan, Fadi F,

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.33 MB

english, 2014

41

Erratum to “A Schistosoma mansoni Pad1 homologue stabilizes c-jun”: [Mol. Biochem. Parasitol. 116 (2001) 209–218]

Joseph F. Nabhan, Fadi F. Hamdan, Paula Ribeiro

Journal:

Molecular and Biochemical Parasitology

Year:

2002

Language:

english

File:

PDF, 39 KB

english, 2002

42

[ASME ASME 2002 21st International Conference on Offshore Mechanics and Arctic Engineering - Oslo, Norway (June 23–28, 2002)] 21st International Conference on Offshore Mechanics and Arctic Engineering, Volume 2 - Margins of Safety in FPSO Hull Strength

Hamdan, Fadi H., Burgan, Bassam A., White, Robert

Year:

2002

Language:

english

File:

PDF, 817 KB

english, 2002

43

FHF1 (FGF12) epileptic encephalopathy: Table

Al-Mehmadi, Sameer, Splitt, Miranda, Ramesh, Venkateswaran, DeBrosse, Suzanne, Dessoffy, Kimberly, Xia, Fan, Yang, Yaping, Rosenfeld, Jill A., Cossette, Patrick, Michaud, Jacques L., Hamdan, Fadi F.,

Journal:

Neurology: Genetics

Year:

2016

Language:

english

File:

PDF, 110 KB

english, 2016

44

Characterization of a Novel Serotonin Receptor from Caenorhabditis elegans : Cloning and Expression of Two Splice Variants

Fadi F. Hamdan, Mark D. Ungrin, Mark Abramovitz, Paula Ribeiro

Journal:

Journal of Neurochemistry

Year:

1999

Language:

english

File:

PDF, 492 KB

english, 1999

45

A Gain-of-Function Mutation in NALCN in a Child with Intellectual Disability, Ataxia, and Arthrogryposis

Aoyagi, Kyota, Rossignol, Elsa, Hamdan, Fadi F., Mulcahy, Ben, Xie, Lin, Nagamatsu, Shinya, Rouleau, Guy A., Zhen, Mei, Michaud, Jacques L.

Journal:

Year:

2015

Language:

english

File:

PDF, 637 KB

english, 2015

46

M₃-muscarinic receptor promotes insulin release via receptor phosphorylation/arrestin-dependent activation of protein kinase D1

Kok Choi Kong, Adrian J. Butcher, Phillip McWilliams, David Jones, Jürgen Wess, Fadi F. Hamdan, Tim Werry, Elizabeth M. Rosethorne, Steven J. Charlton, Sarah E. Munson, Hannah A. Cragg, Alison D. Smar

Journal:

Proceedings of the National Academy of Sciences

Year:

2010

Language:

english

File:

PDF, 1.76 MB

english, 2010

47

Calcitonin Gene-Related Peptide Analogues with Aza and Indolizidinone Amino Acid Residues Reveal Conformational Requirements for Antagonist Activity at the Human Calcitonin Gene-Related Peptide 1 Receptor

Boeglin, Damien, Hamdan, Fadi F., Melendez, Rosa E., Cluzeau, Jérôme, Laperriere, Andre, Héroux, Madeleine, Bouvier, Michel, Lubell, William D.

Journal:

Journal of Medicinal Chemistry

Year:

2007

Language:

english

File:

PDF, 110 KB

english, 2007

48

High retrocaval ureter: An unexpected intraoperative finding during robotic redo pyeloplasty

Junejo, Noor Nabi, Vallasciani, Santiago, Peters, Craig A., AlHazmi, Hamdan, Almathami, Ahmed, Alshammari, Ahmad, AlJallad, Hossam, Azar, Fadi, Abasher, Abdulazeem, AlShahrani, Saeed

Journal:

Urology Case Reports

Year:

2018

Language:

english

File:

PDF, 985 KB

english, 2018

49

Neurotransmitter trafficking defect in a patient with clathrin (CLTC) variation presenting with intellectual disability and early-onset parkinsonism

Manti, Filippo, Nardecchia, Francesca, Barresi, Sabina, Venditti, Martina, Pizzi, Simone, Hamdan, Fadi F., Blau, Nenad, Burlina, Alberto, Tartaglia, Marco, Leuzzi, Vincenzo

Journal:

Parkinsonism & Related Disorders

Year:

2018

Language:

english

File:

PDF, 187 KB

english, 2018

50

De Novo Truncating Mutation in Kinesin 17 Associated with Schizophrenia

Julien Tarabeux, Nathalie Champagne, Edna Brustein, Fadi F. Hamdan, Julie Gauthier, Mathieu Lapointe, Claudia Maios, Amélie Piton, Dan Spiegelman, Édouard Henrion, Bruno Millet, Judith L. Rapoport, Ly

Journal:

Biological Psychiatry

Year:

2010

Language:

english

File:

PDF, 901 KB

english, 2010

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