Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts von Moreno-De-Luca, D, Sanders, S J, Willsey, A J, Mulle, J G, Lowe, J K, Geschwind, D H, State, M W, Martin, C L, Ledbetter, D H

Volltext

Functional evaluation of a PTSD-associated genetic variant: estradiol regulation and ADCYAP1R1 von Mercer, K B, Dias, B, Shafer, D, Maddox, S A, Mulle, J G, Hu, P, Walton, J, Ressler, K J

Volltext

The 3q29 deletion confers >40-fold increase in risk for schizophrenia von Mulle, J G

Volltext

A distinct cognitive profile in individuals with 3q29 deletion syndrome von Klaiman, C., White, S. P., Saulnier, C., Murphy, M., Burrell, L., Cubells, J., Walker, E., Mulle, J. G.

Volltext

Adaptive behaviour deficits in individuals with 3q29 deletion syndrome von Pollak, R. M., Burrell, T. L., Cubells, J. F., Klaiman, C., Murphy, M. M., Saulnier, C. A., Walker, E. F., White, S. P., Mulle, J. G.

Volltext

No evidence for association to the G72 G30 locus in an independent sample of schizophrenia families von Mulle, J G, Chowdari, K V, Nimgaonkar, V, Chakravarti, A

Volltext

Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission von Mulle, J G, Fallin, M D, Lasseter, V K, McGrath, J A, Wolyniec, P S, Pulver, A E

Volltext

Evidence for linkage to chromosome 13q32 in an independent sample of schizophrenia families von Mulle, J G, McDonough, J A, Chowdari, K V, Nimgaonkar, V, Chakravarti, A

Volltext

Bursts of action potential waveforms relieve G-protein inhibition of recombinant P/Q-type Ca2+ channels in HEK 293 cells von Brody, D L, Patil, P G, Mulle, J G, Snutch, T P, Yue, D T

Volltext

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities von Kaminsky, Erin B, Kaul, Vineith, Paschall, Justin, Church, Deanna M, Bunke, Brian, Kunig, Dawn, Moreno-De-Luca, Daniel, Moreno-De-Luca, Andres, Mulle, Jennifer G, Warren, Stephen T, Richard, Gabriele, Compton, John G, Fuller, Amy E, Gliem, Troy J, Huang, Shuwen, Collinson, Morag N, Beal, Sarah J, Ackley, Todd, Pickering, Diane L, Golden, Denae M, Aston, Emily, Whitby, Heidi, Shetty, Shashirekha, Rossi, Michael R, Rudd, M Katharine, South, Sarah T, Brothman, Arthur R, Sanger, Warren G, Iyer, Ramaswamy K, Crolla, John A, Thorland, Erik C, Aradhya, Swaroop, Ledbetter, David H, Martin, Christa L

Volltext

Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions von Mulle, Jennifer Gladys, Sullivan, Patrick F, Hjerling-Leffler, Jens

Volltext

Critical determinants of Ca(2+)-dependent inactivation within an EF-hand motif of L-type Ca(2+) channels von Peterson, B Z, Lee, J S, Mulle, J G, Wang, Y, de Leon, M, Yue, D T

Volltext

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia von Mulle, Jennifer Gladys, Pulver, Ann E, McGrath, John A, Wolyniec, Paula S, Dodd, Anne F, Cutler, David J, Sebat, Jonathan, Malhotra, Dheeraj, Nestadt, Gerald, Conrad, Donald F, Hurles, Matthew, Barnes, Chris P, Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F, Gejman, Pablo V, Sanders, Alan R, Duan, Jubao, Mitchell, Adele A, Peter, Inga, Sklar, Pamela, O’Dushlaine, Colm T, Grozeva, Detelina, O’Donovan, Michael C, Owen, Michael J, Hultman, Christina M, Kähler, Anna K, Sullivan, Patrick F, Kirov, George, Warren, Stephen T

Volltext

Inhibition of Recombinant Ca2+ Channels by Benzothiazepines and Phenylalkylamines: Class-Specific Pharmacology and Underlying Molecular Determinants von Cai, D, Mulle, J G, Yue, D T

Volltext

Critical Determinants of Ca2+-Dependent Inactivation within an EF-Hand Motif of L-Type Ca2+ Channels von Peterson, Blaise Z., Lee, Joanna S., Mulle, Jennifer G., Wang, Yan, de Leon, Marita, Yue, David T.

Volltext

Functional evaluation of a PTSD-associated genetic variant: estradiol regulation and ADCYAP1R1 von Mercer, K B, Dias, B, Shafer, D, Maddox, S A, Mulle, J G, Hu, P, Walton, J, Ressler, K J

Volltext bestellen

A framework for the investigation of rare genetic disorders in neuropsychiatry von Sanders, Stephan J., Sahin, Mustafa, Hostyk, Joseph, Thurm, Audrey, Jacquemont, Sebastien, Avillach, Paul, Douard, Elise, Martin, Christa L., Modi, Meera E., Moreno-De-Luca, Andres, Raznahan, Armin, Anticevic, Alan, Dolmetsch, Ricardo, Feng, Guoping, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Ledbetter, David H., Mulle, Jennifer G., Pasca, Sergiu P., Samaco, Rodney, Sebat, Jonathan, Pariser, Anne, Lehner, Thomas, Gur, Raquel E., Bearden, Carrie E.

Volltext

PEMapper and PECaller provide a simplified approach to whole-genome sequencing von Johnston, H. Richard, Chopra, Pankaj, Wingo, Thomas S., Patel, Viren, Epstein, Michael P., Mulle, Jennifer G., Warren, Stephen T., Zwick, Michael E., Cutler, David J.

Volltext

The Thanatomicrobiome: A Missing Piece of the Microbial Puzzle of Death von Javan, Gulnaz T, Finley, Sheree J, Abidin, Zain, Mulle, Jennifer G

Volltext

Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease von Shaw, Kelly A, Bertha, Madeline, Hofmekler, Tatyana, Chopra, Pankaj, Vatanen, Tommi, Srivatsa, Abhiram, Prince, Jarod, Kumar, Archana, Sauer, Cary, Zwick, Michael E, Satten, Glen A, Kostic, Aleksandar D, Mulle, Jennifer G, Xavier, Ramnik J, Kugathasan, Subra

Volltext