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1

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

2

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

3

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

4

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

5

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

6

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

7

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

8

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

9

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

10

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

11

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

Fadi F. Hamdan, Amélie Piton, Julie Gauthier, Anne Lortie, François Dubeau, Sylvia Dobrzeniecka, Dan Spiegelman, Anne Noreau, Stéphanie Pellerin, Mélanie Côté, Edouard Henrion, Éric Fombonne, Laurent

Journal:

Annals of Neurology

Year:

2009

Language:

english

File:

PDF, 288 KB

english, 2009

12

Cloning and Characterization of a Novel Form of Tyrosine Hydroxylase from the Human Parasite, Schistosoma mansoni

Fadi F. Hamdan, Paula Ribeiro

Journal:

Journal of Neurochemistry

Year:

1998

Language:

english

File:

PDF, 2.02 MB

english, 1998

13

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

14

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

15

Vocal changes following radiotherapy to the head and neck for non-laryngeal tumors

Abdul-latif Hamdan, Fadi Geara, Charbel Rameh, Sami Tanbouzi Husseini, Toufic Eid, Nabil Fuleihan

Journal:

European Archives of Oto-Rhino-Laryngology

Year:

2009

Language:

english

File:

PDF, 225 KB

english, 2009

16

Codon optimization improves heterologous expression of aSchistosoma mansonicDNA in HEK293 cells

Fadi F. Hamdan, Aisha Mousa, Paula Ribeiro

Journal:

Parasitology Research

Year:

2002

Language:

english

File:

PDF, 138 KB

english, 2002

17

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

18

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

19

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

Journal:

Year:

1998

Language:

english

File:

PDF, 999 KB

english, 1998

20

OCCIPITAL BLOCKADE FOR POSTDURAL PUNCTURE HEADACHE: DO WE HARM?

Ahed Zeidan, Fadi Hamdan

Journal:

Year:

2009

Language:

english

File:

PDF, 30 KB

english, 2009

21

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

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

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

24

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, 29 KB

english, 2011

25

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

26

A Schistosoma mansoni Pad1 homologue stabilizes c-Jun

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

Journal:

Molecular and Biochemical Parasitology

Year:

2001

Language:

english

File:

PDF, 623 KB

english, 2001

27

A novel Schistosoma mansoni G protein-coupled receptor is responsive to histamine

Fadi F Hamdan, Mark Abramovitz, Aisha Mousa, Jinling Xie, Yves Durocher, Paula Ribeiro

Journal:

Molecular and Biochemical Parasitology

Year:

2002

Language:

english

File:

PDF, 643 KB

english, 2002

28

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

29

A Schistosoma mansoni Pad1 homologue stabilizes c-Jun

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

Journal:

Molecular and Biochemical Parasitology

Year:

2002

Language:

english

File:

PDF, 494 KB

english, 2002

30

Cloning, Sequencing, and Developmental Expression Levels of a Novel Glutamate-Gated Chloride Channel Homologue in the Parasitic NematodeHaemonchus contortus

Sean G. Forrester, Fadi F. Hamdan, Roger K. Prichard, Robin N. Beech

Journal:

Biochemical and Biophysical Research Communications

Year:

1999

Language:

english

File:

PDF, 305 KB

english, 1999

31

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

32

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

33

Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency

Berryer, Martin H., Hamdan, Fadi F., Klitten, Laura L., Møller, Rikke S., Carmant, Lionel, Schwartzentruber, Jeremy, Patry, Lysanne, Dobrzeniecka, Sylvia, Rochefort, Daniel, Neugnot-Cerioli, Mathilde,

Journal:

Year:

2013

Language:

english

File:

PDF, 530 KB

english, 2013

34

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

35

Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation

Hamdan, Fadi F., Gauthier, Julie, Spiegelman, Dan, Noreau, Anne, Yang, Yan, Pellerin, Stéphanie, Dobrzeniecka, Sylvia, Côté, Mélanie, Perreau-Linck, Elizabeth, Carmant, Lionel, D'Anjou, Guy, Fombonne,

Journal:

Boston Medical and Surgical Journal

Year:

2009

Language:

english

File:

PDF, 654 KB

english, 2009

36

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

37

Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy

Ruzzo, Elizabeth K., Capo-Chichi, José-Mario, Ben-Zeev, Bruria, Chitayat, David, Mao, Hanqian, Pappas, Andrea L., Hitomi, Yuki, Lu, Yi-Fan, Yao, Xiaodi, Hamdan, Fadi F., Pelak, Kimberly, Reznik-Wolf,

Journal:

Year:

2013

Language:

english

File:

PDF, 1.92 MB

english, 2013

38

De novo deletion of FMN2 in a girl with mild non-syndromic intellectual disability

Almuqbil, Mohammed, Hamdan, Fadi F., Mathonnet, Géraldine, Rosenblatt, Bernard, Srour, Myriam

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 363 KB

english, 2013

39

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

40

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

41

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

42

Use of an in Situ Disulfide Cross-Linking Strategy To Map Proximities between Amino Acid Residues in Transmembrane Domains I and VII of the M 3 Muscarinic Acetylcholine Receptor

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

Journal:

Year:

2002

Language:

english

File:

PDF, 226 KB

english, 2002

43

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

44

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

45

CNIH4 Interacts with Newly Synthesized GPCR and Controls Their Export from the Endoplasmic Reticulum

Sauvageau, Etienne, Rochdi, Moulay D., Oueslati, Morad, Hamdan, Fadi F., Percherancier, Yann, Simpson, Jeremy C., Pepperkok, Rainer, Bouvier, Michel

Journal:

Year:

2014

Language:

english

File:

PDF, 9.64 MB

english, 2014

46

[IEEE 2010 IEEE International Solid- State Circuits Conference - (ISSCC) - San Francisco, CA, USA (2010.02.7-2010.02.11)] 2010 IEEE International Solid-State Circuits Conference - (ISSCC) - A 45nm CMOS 13-port 64-word 41b fully associative content-addressable register file

Burda, Greg, Kolla, Yesh, Dieffenderfer, Jim, Hamdan, Fadi

Year:

2010

Language:

english

File:

PDF, 1.49 MB

english, 2010

47

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

48

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

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

Journal:

Proceedings of the National Academy of Sciences

Year:

2010

Language:

english

File:

PDF, 544 KB

english, 2010

49

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

50

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

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