Evidence map›Paper›PMID 37292616›Full record

ArticlemedRxiv : the preprint server for health sciences2023

Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variants.

Corrine Smolen, Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Deepro Banerjee, Laura Rohan, Emily Huber, Laila El Khattabi, Paolo Prontera and 33 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

43 authors at 18 institutions in 6 countries.

Corrine SmolenDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Matthew JensenDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Lisa DyerGeneDx, Gaithersburg, MD 20877, USA.
Lucilla PizzoDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Anastasia TyryshkinaDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Deepro BanerjeeDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Laura RohanDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Emily HuberDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Laila El KhattabiAssistance Publique-Hôpitaux de Paris, Department of Medical Genetics, Armand Trousseau and Pitié-Salpêtrière Hospitals, Paris, France.
Paolo PronteraMedical Genetics Unit, Hospital "Santa Maria della Misericordia", Perugia, Italy.
Jean-Hubert CabergCentre Hospitalier Universitaire de Liège. Domaine Universitaire du Sart Tilman, Liège, Belgium.
Anke Van DijckDepartment of Medical Genetics, University and University Hospital Antwerp, Antwerp, Belgium.
Charles SchwartzGreenwood Genetic Center, Greenwood, SC 29646, USA.
Laurence FaivreCentre de Genetique et Cenre de Référence Anomalies du développement et syndromes malformatifs, Hôpital d'Enfants, CHU Dijon, Dijon, France.
Patrick CallierCentre de Genetique et Cenre de Référence Anomalies du développement et syndromes malformatifs, Hôpital d'Enfants, CHU Dijon, Dijon, France.
Anne-Laure Mosca-BoidronLaboratoire de Genetique Chromosomique et Moleculaire, CHU Dijon, France.
Mathilde LefebvreGAD INSERM UMR1231, FHU TRANSLAD, Université de Bourgogne Franche Comté, Dijon, France.
Kate PopeDepartment of Paediatrics, University of Melbourne, Melbourne, Australia.
Penny SnellDepartment of Paediatrics, University of Melbourne, Melbourne, Australia.
Paul J LockhartDepartment of Paediatrics, University of Melbourne, Melbourne, Australia.
Lucia CastigliaResearch Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Ornella GalesiResearch Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Emanuela AvolaResearch Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Teresa MattinaMedical Genetics, Department of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy.
Marco FicheraResearch Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Giuseppa Maria Luana MandaràMedical Genetics, ASP Ragusa, Ragusa, Italy.
Maria Grazia BruccheriResearch Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Olivier PichonCHU Nantes, Department of Medical Genetics, Nantes, France.
Cedric Le CaignecCHU Toulouse, Department of Medical Genetics, Toulouse, France.
Radka StoevaService de Cytogenetique, CHU de Le Mans, Le Mans, France.
Silvestre CuinatCHU Nantes, Department of Medical Genetics, Nantes, France.
Sandra MercierCHU Nantes, Department of Medical Genetics, Nantes, France.
Claire BénéteauCHU Nantes, Department of Medical Genetics, Nantes, France.
Sophie BlessonDepartment of Genetics, Bretonneau University Hospital, Tours, France.
Ashley NordslettenDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Dominique Martin-CoignardDepartment of Genetics, Bretonneau University Hospital, Tours, France.
Erik SistermansDepartment of Clinical Genetics, Amsterdam UMC, Amsterdam, The Netherlands.
R Frank KooyDepartment of Medical Genetics, University and University Hospital Antwerp, Antwerp, Belgium.
David J AmorBruce Lefroy Center, Murdoch Children's Research Institute, Melbourne, Australia.
Corrado RomanoMedical Genetics, Department of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy.
Bertrand IsidorCHU Nantes, Department of Medical Genetics, Nantes, France.
Jane JuusolaGeneDx, Gaithersburg, MD 20877, USA.
Santhosh GirirajanDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
Pennsylvania State University · USOasi Maria SS · ITInserm · FRThe University of Melbourne · AUUniversity of Catania · ITAntwerp University Hospital · BECentre Hospitalier Universitaire de Tours · FRAmsterdam University Medical Centers · NLCentre Hospitalier du Mans · FRCentre Hospitalier Universitaire de Liège · BEGreenwood Genetic Center · USLaboratoire de Génétique Cellulaire · FRMurdoch Children's Research Institute · AUOspedale Santa Maria · ITSorbonne Université · FRUniversité Toulouse III - Paul Sabatier · FRUniversity of Michigan · USUniversity of Ragusa · IT

Funding

Genomic basis of phenotypic variability of genomic disordersR01GM121907 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI GIRIRAJAN, SANTHOSH · 2017 to 2025
$5.2M
Computation, Bioinformatics, and Statistics (CBIOS) Training ProgramT32GM102057 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI CHIAROMONTE, FRANCESCA, GIRIRAJAN, SANTHOSH · 2013 to 2022
$2.7M
Cellular Basis for Genetic Susceptibility to Neurodevelopmental DisordersR21NS122398 · NINDS · PENNSYLVANIA STATE UNIVERSITY, THE · PI GIRIRAJAN, SANTHOSH · 2021 to 2021
$428k
NIGMS NIH HHS R01 GM121907NIGMS NIH HHS T32 GM102057NINDS NIH HHS R21 NS122398
6 · The paper itself

Abstract

We examined more than 38,000 spouse pairs from four neurodevelopmental disease cohorts and the UK Biobank to identify phenotypic and genetic patterns in parents associated with neurodevelopmental disease risk in children. We identified correlations between six phenotypes in parents and children, including correlations of clinical diagnoses such as obsessive-compulsive disorder (R=0.31-0.49, p<0.001), and two measures of sub-clinical autism features in parents affecting several autism severity measures in children, such as bi-parental mean Social Responsiveness Scale (SRS) scores affecting proband SRS scores (regression coefficient=0.11, p=0.003). We further describe patterns of phenotypic and genetic similarity between spouses, where spouses show both within- and cross-disorder correlations for seven neurological and psychiatric phenotypes, including a within-disorder correlation for depression (R=0.25-0.72, p<0.001) and a cross-disorder correlation between schizophrenia and personality disorder (R=0.20-0.57, p<0.001). Further, these spouses with similar phenotypes were significantly correlated for rare variant burden (R=0.07-0.57, p<0.0001). We propose that assortative mating on these features may drive the increases in genetic risk over generations and the appearance of "genetic anticipation" associated with many variably expressive variants. We further identified parental relatedness as a risk factor for neurodevelopmental disorders through its inverse correlations with burden and pathogenicity of rare variants and propose that parental relatedness drives disease risk by increasing genome-wide homozygosity in children (R=0.09-0.30, p<0.001). Our results highlight the utility of assessing parent phenotypes and genotypes in predicting features in children carrying variably expressive variants and counseling families carrying these variants.

Identifiers

PMID37292616
PMCPMC10246151
OpenAlexW4378532718

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