Hussein Daoud

4.5k citations

58 papers · 2.4k · h-index 24

Impact in

Neurology top 1%
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism
- Parkinson's Disease Mechanisms and Treatments
Genetics top 1%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities

Papers in

Neurology 23
- Amyotrophic Lateral Sclerosis Research 23
- Neurological diseases and metabolism 9
Genetics 15
- Neurogenetic and Muscular Disorders Research 14
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3

Co-authors: Guy A. Rouleau (28 shared papers)Patrick A. Dion (23 shared papers)Paul N. Valdmanis (7 shared papers)William Camu (11 shared papers)Véronique Belzil (13 shared papers)Vincent Meininger (8 shared papers)Nicolas Dupré (10 shared papers)Fadi F. Hamdan (3 shared papers)
Journals: Neurobiology of Aging (6 papers)Journal of Medical Genetics (4 papers)European Journal of Human Genetics (2 papers)Biological Psychiatry (2 papers)Neurology (2 papers)
Partner nations: Canada France United States

In The Last Decade

Hussein Daoud

57 papers receiving 2.4k citations

Peers

Countries citing papers authored by Hussein Daoud

Since Specialization

Citations

This map shows the geographic impact of Hussein Daoud's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hussein Daoud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hussein Daoud more than expected).

Fields of papers citing papers by Hussein Daoud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hussein Daoud. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hussein Daoud. The network helps show where Hussein Daoud may publish in the future.

Co-authors

The 25 scholars most cited alongside Hussein Daoud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hussein Daoud Line = papers co-authored together Hussein Daoud links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	De Novo Mutations in Moderate or Severe Intellectual Disability PLoS Genetics ·Fadi F. Hamdan, Myriam Srour, José‐Mario Capo‐Chichi, Hussein Daoud, Christina Nassif, Lysanne Patry, Christine Massicotte, Amirthagowri Ambalavanan, Dan Spiegelman, Ousmane Diallo, Édouard Henrion, Alexandre Dionne‐Laporte, Anne Fougerat, Alexey V. Pshezhetsky, Sunita Venkateswaran, Guy A. Rouleau, Jacques L. Michaud	2014	265
2	Genetics of motor neuron disorders: new insights into pathogenic mechanisms Nature Reviews Genetics ·Patrick A. Dion, Hussein Daoud, Guy A. Rouleau	2009	228
3	De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment The American Journal of Human Genetics ·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 Lacaille, Laurent Mottron, Pierre Drapeau, Miriam H. Beauchamp, Michael Phillips, Éric Fombonne, Guy A. Rouleau, Jacques L. Michaud	2010	171
4	Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis Journal of Medical Genetics ·Hussein Daoud, Paul N. Valdmanis, Edor Kabashi, Patrick A. Dion, Nicolas Dupré, William Camu, Vincent Meininger, Guy A. Rouleau	2008	155
5	De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism Biological Psychiatry ·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, Laurent Mottron, Miriam H. Beauchamp, Guy A. Rouleau, Jacques L. Michaud	2011	132
6	Mutations in FUS cause FALS and SALS in French and French Canadian populations Neurology ·Véronique Belzil, Paul N. Valdmanis, Patrick A. Dion, Hussein Daoud, Edor Kabashi, Anne Noreau, Julie Gauthier, Pascale Hince, Anne Desjarlais, J.P. Bouchard, Lucette Lacomblez, François Salachas, Pierre Pradat, William Camu, Vincent Meininger, Nicolas Dupré, Guy A. Rouleau	2009	114
7	Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis Human Molecular Genetics ·Hannah Kaneb, Andrew W. Folkmann, Véronique Belzil, Li-En Jao, Claire S. Leblond, Simon Girard, Hussein Daoud, Anne Noreau, Daniel Rochefort, Pascale Hince, Anna Szuto, Annie Levert, Sabrina Vidal, Catherine André-Guimont, William Camu, Jean-Pierre Bouchard, Nicolas Dupré, Guy A. Rouleau, Susan R. Wente, Patrick A. Dion	2014	102
8	Recent advances in the genetics of amyotrophic lateral sclerosis Current Neurology and Neuroscience Reports ·Paul N. Valdmanis, Hussein Daoud, Patrick A. Dion, Guy A. Rouleau	2009	95
9	Exome sequencing reveals SPG11 mutations causing juvenile ALS Neurobiology of Aging ·Hussein Daoud, Sirui Zhou, Anne Noreau, Mike Sabbagh, Véronique Belzil, Alexandre Dionne‐Laporte, Christine Tranchant, Patrick A. Dion, Guy A. Rouleau	2011	75
10	Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism Journal of Medical Genetics ·Hussein Daoud, Martine Tétreault, William T. Gibson, Kether Guerrero, Ana S.A. Cohen, Janina Gburek‐Augustat, Matthis Synofzik, Bernard Brais, Cathy A. Stevens, Rocı́o Sánchez-Carpintero, Cyril Goizet, Sakkubai Naidu, Adeline Vanderver, Geneviève Bernard	2013	71
11	Association of Long ATXN2 CAG Repeat Sizes With Increased Risk of Amyotrophic Lateral Sclerosis Archives of Neurology ·Hussein Daoud, Véronique Belzil, Sandra Martins, Mike Sabbagh, Pierre Provencher, Lucette Lacomblez, Vincent Meininger, William Camu, Nicolas Dupré, Patrick A. Dion, Guy A. Rouleau	2011	69
12	Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit Canadian Medical Association Journal ·Hussein Daoud, Stephanie M. Luco, Rui Li, Eric Bareke, Chandree L. Beaulieu, Olga Jarinova, Nancy Carson, Sarah M. Nikkel, Gail E. Graham, Julie Richer, Christine M. Armour, Dennis E. Bulman, Pranesh Chakraborty, Michael T. Geraghty, Matthew A. Lines, Thierry Lacaze‐Masmonteil, Jacek Majewski, Kym M. Boycott, David A. Dyment	2016	68
13	Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations Neurology ·Philippe Corcia, Paul N. Valdmanis, Stéphanie Millecamps, Claire Lionnet, Hélène Blasco, Kévin Mouzat, Hussein Daoud, Véronique Belzil, Raúl Juntas Morales, N. Pageot, Véronique Danel-Brunaud, N. Vandenberghe, Pierre Pradat, Philippe Couratier, François Salachas, Serge Lumbroso, Guy A. Rouleau, Vincent Meininger, William Camu	2012	67
14	Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients Gene ·Paloma González-Pérez, Ute Woehlbier, Ru-Ju Chian, Peter C. Sapp, Guy A. Rouleau, Claire S. Leblond, Hussein Daoud, Patrick A. Dion, John E. Landers, Claudio Hetz, Robert H. Brown	2015	59
15	Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay Journal of Medical Genetics ·Hussein Daoud, Dong Zhang, Fiona McMurray, Andrea C. Yu, Stephanie M. Luco, Jason Vanstone, Olga Jarinova, Nancy Carson, James R. Wickens, Shifali Shishodia, Hwanho Choi, M.A. McDonough, Christopher J. Schofield, Mary‐Ellen Harper, David A. Dyment, Christine M. Armour	2015	51
16	Autism and Nonsyndromic Mental Retardation Associated with a De Novo Mutation in the NLGN4X Gene Promoter Causing an Increased Expression Level Biological Psychiatry ·Hussein Daoud, Frédérique Bonnet‐Brilhault, Sylviane Védrine, Marie-Véronique Demattei, Patrick Vourc’h, Nadia Bayou, Christian Andrés, Catherine Barthélémy, Frédéric Laumonnier, Sylvain Briault	2009	48
17	Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis Neurobiology of Aging ·Véronique Belzil, Hussein Daoud, Anne Desjarlais, Jean-Pierre Bouchard, Nicolas Dupré, William Camu, Patrick A. Dion, Guy A. Rouleau	2010	43
18	Resequencing of 29 Candidate Genes in Patients With Familial and Sporadic Amyotrophic Lateral Sclerosis Archives of Neurology ·Hussein Daoud, Paul N. Valdmanis, François Gros‐Louis, Véronique Belzil, Dan Spiegelman, Édouard Henrion, Ousmane Diallo, Anne Desjarlais, Julie Gauthier, William Camu, Patrick A. Dion, Guy A. Rouleau	2011	41
19	UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis Neurobiology of Aging ·Hussein Daoud, Hamid Suhail, Anna Szuto, William Camu, François Salachas, Vincent Meininger, Jean‐Pierre Bouchard, Nicolas Dupré, Patrick A. Dion, Guy A. Rouleau	2012	39
20	Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature BMC Medical Genetics ·Stephanie M. Luco, Daniela Pohl, Erick Sell, Justin D. Wagner, David A. Dyment, Hussein Daoud	2016	35

About Hussein Daoud

Hussein Daoud is a scholar working on Neurology, Genetics, Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine, having authored 58 papers that have together received 2.4k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (23 papers), Neurogenetic and Muscular Disorders Research (14 papers), Neurological diseases and metabolism (9 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (4 papers), Autism Spectrum Disorder Research (3 papers), Metabolism and Genetic Disorders (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Neurology (947 citations), Genetics (552 citations), Neurology (297 citations), Genetics (560 citations) and Cellular and Molecular Neuroscience (329 citations). Hussein Daoud has collaborated with scholars based in Canada, France and United States. Frequent co-authors include Guy A. Rouleau, Patrick A. Dion, Paul N. Valdmanis, William Camu, Véronique Belzil, Vincent Meininger, Nicolas Dupré, Fadi F. Hamdan, Jacques L. Michaud and Alexandre Dionne‐Laporte. Their work appears in journals such as Neurobiology of Aging, Journal of Medical Genetics, European Journal of Human Genetics, Biological Psychiatry and Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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