Anne Maillard-Wermelinger

Publications | Phd and Masters theses

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22 publications

2023 | 2021 | 2019 | 2018 | 2017 | 2016 | 2015 | 2012 | 2009 |
2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research.
White L.K., Crowley T.B., Finucane B., McClellan E.J., Donoghue S., Garcia-Minaur S., Repetto G.M., Fischer M., Jacquemont S., Gur R.E. et al., 2023/01/07. Genes, 14 (1) p. 169. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_F4192F47B167]
2021
Sex differences in sensory processing in children with autism spectrum disorder.
Osório JMA, Rodríguez-Herreros B., Richetin S., Junod V., Romascano D., Pittet V., Chabane N., Jequier Gygax M., Maillard A.M., 2021/11. Autism research, 14 (11) pp. 2412-2423. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_EB9B693703B8]
Uncovering the Mechanisms of Real‐World Attentional Control Over the Course of Primary Education
Turoman Nora, Tivadar Ruxandra I., Retsa Chrysa, Maillard Anne M., Scerif Gaia, Matusz Pawel J., 2021/11. Mind, Brain, and Education, 15 (4) pp. 344-353.
[URN][DOI][WoS][serval:BIB_4957A4E29E6D]
Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication.
Linden S.C., Watson C.J., Smith J., Chawner SJRA, Lancaster T.M., Evans F., Williams N., Skuse D., Raymond F.L., Hall J. et al., 2021/06/18. Translational psychiatry, 11 (1) p. 372. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8BDA2BB50C97]
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
Sønderby I.E., van der Meer D., Moreau C., Kaufmann T., Walters G.B., Ellegaard M., Abdellaoui A., Ames D., Amunts K., Andersson M. et al., 2021/03/22. Translational psychiatry, 11 (1) p. 182. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_89117CC8B7BA]
Touch and olfaction/taste differentiate children carrying a 16p11.2 deletion from children with ASD.
Osório JMA, Rodríguez-Herreros B., Romascano D., Junod V., Habegger A., Pain A., Richetin S., Yu P., Isidor B., Van Maldergem L. et al., 2021/02/05. Molecular autism, 12 (1) p. 8. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8C260339EF96]
 
The psychiatric phenotypes of 1q21 distal deletion and duplication.
Linden S.C., Watson C.J., Smith J., Chawner SJRA, Lancaster T.M., Evans F., Williams N., Skuse D., Raymond F.L., Hall J. et al., 2021/02/04. Translational psychiatry, 11 (1) p. 105. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_FC04B9867C5C]
2019
 
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication.
Niarchou M., Chawner SJRA, Doherty J.L., Maillard A.M., Jacquemont S., Chung W.K., Green-Snyder L., Bernier R.A., Goin-Kochel R.P., Hanson E. et al., 2019/03/05..
[DOI][WoS][Pmid][serval:BIB_F226247C7F6B]
Psychiatric disorders in children with 16p11.2 deletion and duplication.
Niarchou M., Chawner SJRA, Doherty J.L., Maillard A.M., Jacquemont S., Chung W.K., Green-Snyder L., Bernier R.A., Goin-Kochel R.P., Hanson E. et al., 2019/01/16. Translational psychiatry, 9 (1) p. 8. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_7215F92283AE]
2018
Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
Martin-Brevet S., Rodríguez-Herreros B., Nielsen J.A., Moreau C., Modenato C., Maillard A.M., Pain A., Richetin S., Jønch A.E., Qureshi A.Y. et al., 2018/08/15. Biological psychiatry, 84 (4) pp. 253-264. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8964BF69CE74]
2017
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.
Loviglio M.N., Leleu M., Männik K., Passeggeri M., Giannuzzi G., van der Werf I., Waszak S.M., Zazhytska M., Roberts-Caldeira I., Gheldof N. et al., 2017. Molecular Psychiatry, 22 (6) pp. 836-849. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8773892CB036]
 
Facteurs étiologiques et co-morbidités des troubles du spectre autistique (TSA)
Jequier Gygax M., Maillard A.M., 2017. Pediatrica.
[serval:BIB_84E05B0FB9EF]
 
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs.
Loviglio M.N., Arbogast T., Jønch A.E., Collins S.C., Popadin K., Bonnet C.S., Giannuzzi G., Maillard A.M., Jacquemont S., 16p11.2 Consortium et al., 2017. American Journal of Human Genetics, 101 (4) pp. 564-577. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_12249EC890B3]
2016
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Hippolyte L., Maillard A.M., Rodriguez-Herreros B., Pain A., Martin-Brevet S., Ferrari C., Conus P., Macé A., Hadjikhani N., Metspalu A. et al., 2016/07/15. Biological psychiatry, 80 (2) pp. 129-139. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_9660DE6D30D1]
 
16p11.2 Locus modulates response to satiety before the onset of obesity.
Maillard A.M., Hippolyte L., Rodriguez-Herreros B., Chawner S.J., Dremmel D., Agüera Z., Fagundo A.B., Pain A., Martin-Brevet S., Hilbert A. et al., 2016/05. International journal of obesity, 40 (5) pp. 870-876. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_DF2B3B0B794D]
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
D'Angelo D., Lebon S., Chen Q., Martin-Brevet S., Snyder L.G., Hippolyte L., Hanson E., Maillard A.M., Faucett W.A., Macé A. et al., 2016. Jama Psychiatry, 73 (1) pp. 20-30. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_FA7E8A43283E]
 
Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants
Leitsalu L., Alavere H., Jacquemont S., Kolk A., Maillard A.M., Reigo A., Noukas M., Reymond A., Mannik K., Ng P.C. et al., 2016. Personalized Medicine, 13 (4) pp. 303-314.
[DOI][WoS][serval:BIB_3FBCEB3A9F4A]
2015
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
Maillard A.M., Ruef A., Pizzagalli F., Migliavacca E., Hippolyte L., Adaszewski S., Dukart J., Ferrari C., Conus P., Männik K. et al., 2015/02. Molecular psychiatry, 20 (1) pp. 140-147. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_02ADC1E92D32]
 
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology.
Migliavacca E., Golzio C., Männik K., Blumenthal I., Oh E.C., Harewood L., Kosmicki J.A., Loviglio M.N., Giannuzzi G., Hippolyte L. et al., 2015. American Journal of Human Genetics, 96 (5) pp. 784-796.
[DOI][WoS][Pmid][serval:BIB_9689D2C97A3A]
Copy number variations and cognitive phenotypes in unselected populations
Männik K., Mägi R., Macé A., Cole B., Guyatt A.L., Shihab H.A., Maillard A.M., Alavere H., Kolk A., Reigo A. et al., 2015. Journal of the American Medical Association, 313 (20) pp. 2044-2054. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_C20E4A2E4D67]
2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Zufferey F., Sherr E.H., Beckmann N.D., Hanson E., Maillard A.M., Hippolyte L., Macé A., Ferrari C., Kutalik Z., Andrieux J. et al., 2012. Journal of Medical Genetics, 49 (10) pp. 660-668. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_26004E3F396F]
2009
Mild traumatic brain injury and executive functions in school-aged children.
Maillard-Wermelinger A., Yeates K.O., Gerry Taylor H., Rusin J., Bangert B., Dietrich A., Nuss K., Wright M., 2009. Developmental neurorehabilitation, 12 (5) pp. 330-341. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_20716F167782]
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