| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1417 | 2018 |
| Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa HJ Watson, Z Yilmaz, LM Thornton, C Hübel, JRI Coleman, HA Gaspar, ... Nature genetics 51 (8), 1207-1214, 2019 | 880 | 2019 |
| Investigating neural primacy in Major Depressive Disorder: multivariate Granger causality analysis of resting-state fMRI time-series data JP Hamilton, G Chen, ME Thomason, ME Schwartz, IH Gotlib Molecular psychiatry 16 (7), 763-772, 2011 | 714* | 2011 |
| A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2 RG Walters, S Jacquemont, A Valsesia, AJ de Smith, D Martinet, ... Nature 463 (7281), 671-675, 2010 | 612 | 2010 |
| Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11. 2 locus S Jacquemont, A Reymond, F Zufferey, L Harewood, RG Walters, ... Nature 478 (7367), 97-102, 2011 | 541 | 2011 |
| A 600 kb deletion syndrome at 16p11. 2 leads to energy imbalance and neuropsychiatric disorders F Zufferey, EH Sherr, ND Beckmann, E Hanson, AM Maillard, L Hippolyte, ... Journal of medical genetics 49 (10), 660-668, 2012 | 317 | 2012 |
| Defining the effect of the 16p11. 2 duplication on cognition, behavior, and medical comorbidities D D’Angelo, S Lebon, Q Chen, S Martin-Brevet, LAG Snyder, L Hippolyte, ... JAMA psychiatry 73 (1), 20-30, 2016 | 244 | 2016 |
| Fourteen new cases contribute to the characterization of the 7q11. 23 microduplication syndrome N Van der Aa, L Rooms, G Vandeweyer, J van den Ende, E Reyniers, ... European journal of medical genetics 52 (2-3), 94-100, 2009 | 232 | 2009 |
| The 16p11. 2 locus modulates brain structures common to autism, schizophrenia and obesity AM Maillard, A Ruef, F Pizzagalli, E Migliavacca, L Hippolyte, ... Molecular psychiatry 20 (1), 140-147, 2015 | 206 | 2015 |
| Copy number variations and cognitive phenotypes in unselected populations K Männik, R Mägi, A Macé, B Cole, AL Guyatt, HA Shihab, AM Maillard, ... Jama 313 (20), 2044-2054, 2015 | 177 | 2015 |
| Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants L Pizzo, M Jensen, A Polyak, JA Rosenfeld, K Mannik, A Krishnan, ... Genetics in Medicine 21 (4), 816-825, 2019 | 171 | 2019 |
| Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ... Biological psychiatry 91 (3), 313-327, 2022 | 164 | 2022 |
| The number of genomic copies at the 16p11. 2 locus modulates language, verbal memory, and inhibition L Hippolyte, AM Maillard, B Rodriguez-Herreros, A Pain, S Martin-Brevet, ... Biological psychiatry 80 (2), 129-139, 2016 | 100 | 2016 |
| Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes MN Loviglio, M Leleu, K Männik, M Passeggeri, G Giannuzzi, ... Molecular Psychiatry 22 (6), 836-849, 2017 | 95 | 2017 |
| Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index A Hinney, M Kesselmeier, S Jall, AL Volckmar, M Föcker, J Antel, IM Heid, ... Molecular psychiatry 22 (2), 192-201, 2017 | 87 | 2017 |
| 16p11. 2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy EM Reinthaler, D Lal, S Lebon, MS Hildebrand, HHM Dahl, BM Regan, ... Human molecular genetics 23 (22), 6069-6080, 2014 | 80 | 2014 |
| A potential contributory role for ciliary dysfunction in the 16p11. 2 600 kb BP4-BP5 pathology E Migliavacca, C Golzio, K Männik, I Blumenthal, EC Oh, L Harewood, ... The American Journal of Human Genetics 96 (5), 784-796, 2015 | 70 | 2015 |
| Increased Dosage of RAB 39 B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal X q28 Copy Number Gains L Vanmarsenille, M Giannandrea, N Fieremans, J Verbeeck, S Belet, ... Human mutation 35 (3), 377-383, 2014 | 66 | 2014 |
| Associations between attention-deficit/hyperactivity disorder and various eating disorders: a Swedish nationwide population study using multiple genetically informative approaches S Yao, R Kuja-Halkola, J Martin, Y Lu, P Lichtenstein, C Norring, ... Biological psychiatry 86 (8), 577-586, 2019 | 58 | 2019 |
| Shared genetic risk between eating disorder‐and substance‐use‐related phenotypes: Evidence from genome‐wide association studies MA Munn‐Chernoff, EC Johnson, YL Chou, JRI Coleman, LM Thornton, ... Addiction biology 26 (1), e12880, 2021 | 57 | 2021 |
