The Role of Inflammatory Cytokines, the RANKL/OPG Axis, and the Immunoskeletal Interface in Physiological Bone Turnover and Osteoporosis

by M. Neale Weitzmann
Published 2013-01-01

Recent advances in understanding of attention deficit hyperactivity disorder (ADHD): how genetics are shaping our conceptualization of this disorder [version 1; peer review: 3 appr...

by Tetyana Zayats, Benjamin M Neale
Published 2019-12-01

Recent advances in understanding of attention deficit hyperactivity disorder (ADHD): how genetics are shaping our conceptualization of this disorder [version 2; peer review: 3 appr...

by Tetyana Zayats, Benjamin M Neale
Published 2020-02-01

Effects of drought on groundwater-fed lake areas in the Nebraska Sand Hills

by Nawaraj Shrestha, Aaron R. Mittelstet, Troy E. Gilmore, Vitaly Zlotnik, Christopher M. Neale
Published 2021-08-01

Human genetic analyses of organelles highlight the nucleus in age-related trait heritability

by Rahul Gupta, Konrad J Karczewski, Daniel Howrigan, Benjamin M Neale, Vamsi K Mootha
Published 2021-09-01

Correction: Phenome-wide heritability analysis of the UK Biobank.

by Tian Ge, Chia-Yen Chen, Benjamin M Neale, Mert R Sabuncu, Jordan W Smoller
Published 2018-02-01

Phenome-wide heritability analysis of the UK Biobank.

by Tian Ge, Chia-Yen Chen, Benjamin M Neale, Mert R Sabuncu, Jordan W Smoller
Published 2017-04-01

Aligning health and welfare principles and practice in organic dairy systems: a review

by C.L. Marley, R.F. Weller, M. Neale, D.C.J. Main, S. Roderick, R. Keatinge
Published 2010-01-01

Disruption of PTH receptor 1 in T cells protects against PTH-induced bone loss.

by Hesham Tawfeek, Brahmchetna Bedi, Jau-Yi Li, Jonathan Adams, Tatsuya Kobayashi, M Neale Weitzmann, Henry M Kronenberg, Roberto Pacifici
Published 2010-08-01

GNB3 overexpression causes obesity and metabolic syndrome.

by Alev Cagla Ozdemir, Grace M Wynn, Aimee Vester, M Neale Weitzmann, Gretchen N Neigh, Shanthi Srinivasan, M Katharine Rudd
Published 2017-01-01

PTH induces bone loss via microbial-dependent expansion of intestinal TNF+ T cells and Th17 cells

by Mingcan Yu, Abdul Malik Tyagi, Jau-Yi Li, Jonathan Adams, Timothy L. Denning, M. Neale Weitzmann, Rheinallt M. Jones, Roberto Pacifici
Published 2020-01-01

Testing for an unusual distribution of rare variants.

by Benjamin M Neale, Manuel A Rivas, Benjamin F Voight, David Altshuler, Bernie Devlin, Marju Orho-Melander, Sekar Kathiresan, Shaun M Purcell, Kathryn Roeder, Mark J Daly
Published 2011-03-01

Dysregulated B cell expression of RANKL and OPG correlates with loss of bone mineral density in HIV infection.

by Kehmia Titanji, Aswani Vunnava, Anandi N Sheth, Cecile Delille, Jeffrey L Lennox, Sara E Sanford, Antonina Foster, Andrea Knezevic, Kirk A Easley, M Neale Weitzmann, Ighovwerha Ofotokun
Published 2014-10-01

Metabolomic Associations with Serum Bone Turnover Markers

by Moriah P. Bellissimo, Joseph L. Roberts, Dean P. Jones, Ken H. Liu, Kaitlin R. Taibl, Karan Uppal, M. Neale Weitzmann, Roberto Pacifici, Hicham Drissi, Thomas R. Ziegler, Jessica A. Alvarez
Published 2020-10-01

Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

by Rossella Spataro, Maria Kousi, Sali M. K. Farhan, Jason R. Willer, Jay P. Ross, Patrick A. Dion, Guy A. Rouleau, Mark J. Daly, Benjamin M. Neale, Vincenzo La Bella, Nicholas Katsanis
Published 2019-04-01

Runs of homozygosity implicate autozygosity as a schizophrenia risk factor.

by Matthew C Keller, Matthew A Simonson, Stephan Ripke, Ben M Neale, Pablo V Gejman, Daniel P Howrigan, Sang Hong Lee, Todd Lencz, Douglas F Levinson, Patrick F Sullivan, Schizophrenia Psychiatric Genome-Wide Association Study Consortium
Published 2012-01-01

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

by Allison A. Regier, Yossi Farjoun, David E. Larson, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan, Bo-Juen Chen, Manisha Kher, Eric Banks, Darren C. Ames, Adam C. English, Heng Li, Jinchuan Xing, Yeting Zhang, Tara Matise, Goncalo R. Abecasis, Will Salerno, Michael C. Zody, Benjamin M. Neale, Ira M. Hall
Published 2018-10-01

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti...

by John D Murdoch, Abha R Gupta, Stephan J Sanders, Michael F Walker, John Keaney, Thomas V Fernandez, Michael T Murtha, Samuel Anyanwu, Gordon T Ober, Melanie J Raubeson, Nicholas M DiLullo, Natalie Villa, Zainabdul Waqar, Catherine Sullivan, Luis Gonzalez, A Jeremy Willsey, So-Yeon Choe, Benjamin M Neale, Mark J Daly, Matthew W State
Published 2015-01-01

Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

by Ditte Demontis, Raymond K. Walters, Veera M. Rajagopal, Irwin D. Waldman, Jakob Grove, Thomas D. Als, Søren Dalsgaard, Marta Ribasés, Jonas Bybjerg-Grauholm, Maria Bækvad-Hansen, Thomas Werge, Merete Nordentoft, Ole Mors, Preben Bo Mortensen, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Bru Cormand, David M. Hougaard, Benjamin M. Neale, Barbara Franke, Stephen V. Faraone, Anders D. Børglum
Published 2021-02-01

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

by Ditte Demontis, Raymond K. Walters, Veera M. Rajagopal, Irwin D. Waldman, Jakob Grove, Thomas D. Als, Søren Dalsgaard, Marta Ribasas, Jonas Bybjerg-Grauholm, Maria Bækvad-Hansen, Thomas Werge, Merete Nordentoft, Ole Mors, Preben Bo Mortensen, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Bru Cormand, David M. Hougaard, Benjamin M. Neale, Barbara Franke, Stephen V. Faraone, Anders D. Børglum
Published 2021-01-01