Lysanne Patry

2.6k citations

16 papers · 1.0k indexed · h-index 14

Co-authors: Jacques L. Michaud Guy A. Rouleau Fadi F. Hamdan José‐Mario Capo‐Chichi Myriam Srour Christine Massicotte Mark E. Samuels Jeremy Schwartzentruber
Topics: Mitochondrial Function and Pathology (4 papers)Hedgehog Signaling Pathway Studies (3 papers)Genetic and Kidney Cyst Diseases (3 papers)
Cited by: Genetics Molecular Biology Cellular and Molecular Neuroscience
Journals: The Journal of Clinical Endocrinology & Metabolism The American Journal of Human Genetics Human Molecular Genetics
Partner nations: Canada United States Italy

In The Last Decade

Lysanne Patry

16 papers receiving 987 citations

Peers

Countries citing papers authored by Lysanne Patry

Since Specialization

Citations

This map shows the geographic impact of Lysanne Patry'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 Lysanne Patry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lysanne Patry more than expected).

Fields of papers citing papers by Lysanne Patry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lysanne Patry. 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 Lysanne Patry. The network helps show where Lysanne Patry may publish in the future.

Co-authorship network of co-authors of Lysanne Patry

This figure shows the co-authorship network connecting the top 25 collaborators of Lysanne Patry. A scholar is included among the top collaborators of Lysanne Patry based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lysanne Patry. Lysanne Patry is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA SynthetaseIARS2in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome 2015 ·Human Mutation ·Jeremy Schwartzentruber,Daniela Buhaş,Jacek Majewski,Florin Sasarman,Simon Papillon‐Cavanagh,Isabelle Thiffault,Katherine Sheldon,Christine Massicotte,Lysanne Patry,Mariella Simon,Amir S. Zare,Kevin McKernan,Jacques L. Michaud,Richard G. Boles,Cheri Deal,Valérie Désilets,Eric A. Shoubridge,Mark E. Samuels	1
2	Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria 2015 ·Journal of Medical Genetics ·José‐Mario Capo‐Chichi,Sarah Boissel,Edna Brustein,Sarah Pickles,Catherine Fallet‐Bianco,Christina Nassif,Lysanne Patry,Sylvia Dobrzeniecka,Meijiang Liao,Damian Labuda,Mark E. Samuels,Fadi F. Hamdan,Christine Vande Velde,Guy A. Rouleau,Pierre Drapeau,Jacques L. Michaud	29
3	De Novo Mutations in Moderate or Severe Intellectual Disability 2014 ·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	259
4	Mutations in NFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies 2014 ·BMC Medical Genetics ·Thierry Brue,(unknown),Konstantin Khetchoumian,(unknown),José‐Mario Capo‐Chichi,Brigitte Delemer,Aurélio Balsalobre,Christina Nassif,Dimitrios T. Papadimitriou,Anne Pagnier,(unknown),Lysanne Patry,Jeremy Schwartzentruber,Pierre‐François Souchon,Shinobu Takayasu,A Enjalbert,Guy Van Vliet,Jacek Majewski,Jacques Drouin,Mark E. Samuels	54
5	Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA SynthetaseIARS2in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome 2014 ·Human Mutation ·Jeremy Schwartzentruber,Daniela Buhaş,Jacek Majewski,Florin Sasarman,Simon Papillon‐Cavanagh,(unknown),Katherine Sheldon,Christine Massicotte,Lysanne Patry,Mariella Simon,Amir S. Zare,Kevin McKernan,Jacques L. Michaud,Richard G. Boles,Cheri Deal,Valérie Désilets,Eric A. Shoubridge,Mark E. Samuels	61
6	Hajdu–Cheney syndrome 2014 ·Clinical Dysmorphology ·Maria Descartes,Kitiwan Rojnueangnit,(unknown),Amelia Sutton,Sarah Morgan,Lysanne Patry,Mark Samuels	24
7	SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth 2013 ·Human Molecular Genetics ·Anna Corradi,Manuela Fadda,Amélie Piton,Lysanne Patry,Antonella Marte,Pia Rossi,Maxime Cadieux‐Dion,Julie Gauthier,Line Lapointe,Laurent Mottron,Flavia Valtorta,Guy A. Rouleau,Anna Fassio,Fabio Benfenati,Patrick Cossette	65
8	Bioinactive ACTH Causing Glucocorticoid Deficiency 2013 ·The Journal of Clinical Endocrinology & Metabolism ·Mark E. Samuels,Nicole Gallo‐Payet,(unknown),(unknown),(unknown),Lysanne Patry,L. A. Chouinard,Jeremy Schwartzentruber,Patricia René,Nicole Sawyer,Michel Bouvier,Anissa Djemli,Edgard Delvin,Céline Huot,(unknown),Cheri Deal,Guy Van Vliet,Jacek Majewski,Johnny Deladoëy	37
9	Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia 2013 ·The American Journal of Human Genetics ·Myriam Srour,David Chitayat,Véronique Caron,Nicolas Chassaing,Pierre Bitoun,Lysanne Patry,Marie‐Pierre Cordier,José‐Mario Capo‐Chichi,Christine Francannet,Patrick Calvas,Nicola Ragge,Sylvia Dobrzeniecka,Fadi F. Hamdan,Guy A. Rouleau,André Tremblay,Jacques L. Michaud	74
10	Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia 2013 ·The American Journal of Human Genetics ·Myriam Srour,David Chitayat,Véronique Caron,Nicolas Chassaing,Pierre Bitoun,Lysanne Patry,Marie‐Pierre Cordier,José‐Mario Capo‐Chichi,Christine Francannet,Patrick Calvas,Nicola Ragge,Sylvia Dobrzeniecka,Fadi F. Hamdan,Guy A. Rouleau,André Tremblay,Jacques L. Michaud	3
11	Disruption of TBC1D7, a subunit of the TSC1-TSC2 protein complex, in intellectual disability and megalencephaly 2013 ·Journal of Medical Genetics ·José‐Mario Capo‐Chichi,Joseph Tcherkezian,Fadi F. Hamdan,(unknown),Sylvia Dobrzeniecka,Lysanne Patry,(unknown),Bettina E. Mucha,Philippe Major,Michael Shevell,Bouchra Ouled Amar Bencheikh,Ridha Joober,Mark E. Samuels,Guy A. Rouleau,Philippe P. Roux,Jacques L. Michaud	36
12	Mutations in TMEM231 cause Joubert syndrome in French Canadians 2012 ·Journal of Medical Genetics ·Myriam Srour,Fadi F. Hamdan,Jeremy Schwartzentruber,Lysanne Patry,Luis H. Ospina,Michael Shevell,Valérie Désilets,Sylvia Dobrzeniecka,Géraldine Mathonnet,Emmanuelle Lemyre,Christine Massicotte,Damian Labuda,Dina Amrom,Eva Andermann,Guillaume Sébire,Bruno Maranda,Guy A. Rouleau,Jacek Majewski,Jacques L. Michaud	49
13	Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population 2012 ·The American Journal of Human Genetics ·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. Samuels,Kym M. Boycott,Michael Shevell,Rachel Laframboise,Valérie Désilets,Bruno Maranda,Guy A. Rouleau,Jacek Majewski,Jacques L. Michaud	92
14	Identification and Biochemical Characterization of a Novel Mutation inDDX11Causing Warsaw Breakage Syndrome 2012 ·Human Mutation ·José‐Mario Capo‐Chichi,Sanjay Kumar Bharti,Joshua A. Sommers,Tony Yammine,Éliane Chouery,Lysanne Patry,Guy A. Rouleau,Mark Samuels,Fadi F. Hamdan,Jacques L. Michaud,Robert M. Brosh,André Mégarbané,Zoha Kibar	76
15	Mutations in NOTCH2 in families with Hajdu-Cheney syndrome 2011 ·Human Mutation ·Jacek Majewski,Jeremy Schwartzentruber,Aurore Caqueret,Lysanne Patry,Janet Marcadier,Jean‐Pierre Fryns,Kym M. Boycott,Louis‐Georges Ste‐Marie,Fergus E. McKiernan,(unknown),Hilde Van Esch,Jacques L. Michaud,Mark E. Samuels	81
16	Absence of a differentiation defect in muscle satellite cells from DM2 patients 2009 ·Neurobiology of Disease ·Richard Pelletier,Frédéric Hamel,(unknown),Lysanne Patry,(unknown),Mark A. Tarnopolsky,Benedikt Schoser,Jack Puymirat	64

About Lysanne Patry

Lysanne Patry is a scholar working on Genetics, Molecular Biology and Endocrine and Autonomic Systems, having authored 16 papers that have together received 1.0k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (4 papers), Hedgehog Signaling Pathway Studies (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). The work is most often cited by research in Genetics (480 citations), Molecular Biology (671 citations) and Cellular and Molecular Neuroscience (138 citations). Lysanne Patry has collaborated with scholars based in Canada, United States and Italy. Frequent co-authors include Jacques L. Michaud, Guy A. Rouleau, Fadi F. Hamdan, José‐Mario Capo‐Chichi, Myriam Srour, Christine Massicotte, Mark E. Samuels, Jeremy Schwartzentruber, Jacek Majewski and Christina Nassif. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Human Molecular Genetics.

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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