Computing power of quantitative trait locus association mapping for haploid loci

Por Gordon, Derek, Zinn, Andrew R
Publicado em 2009

A Second Recombination Hotspot Associated with SHOX Deletions

Por Zinn, Andrew R., Ramos, Purita, Ross, Judith L.
Publicado em 2006

Reply to Benito-Sanz et al.

Por Zinn, Andrew R., Ramos, Purita, Ross, Judith L.
Publicado em 2006

Sim1 Inhibits Bone Formation by Enhancing the Sympathetic Tone in Male Mice

Por Wang, Xunde, Wei, Wei, Zinn, Andrew R., Wan, Yihong
Publicado no Endocrinology (2015)

The Turner Syndrome–Associated Neurocognitive Phenotype Maps to Distal Xp

Por Ross, Judith L., Roeltgen, David, Kushner, Harvey, Wei, Fanglin, Zinn, Andrew R.
Publicado em 2000

Oxytocin Deficiency Mediates Hyperphagic Obesity of Sim1 Haploinsufficient Mice

Por Kublaoui, Bassil M., Gemelli, Terry, Tolson, Kristen P., Wang, Yu, Zinn, Andrew R.
Publicado em 2008

Inducible Neuronal Inactivation of Sim1 in Adult Mice Causes Hyperphagic Obesity

Por Tolson, Kristen P., Gemelli, Terry, Meyer, Donna, Yazdani, Umar, Kozlitina, Julia, Zinn, Andrew R.
Publicado em 2014

An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome

Por Ross, Judith L., Zeger, Martha P.D., Kushner, Harvey, Zinn, Andrew R., Roeltgen, David P.
Publicado em 2009

MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes

Por Bhoj, Elizabeth J, Romeo, Stefano, Baroni, Marco G, Bartov, Guy, Schultz, Roger A, Zinn, Andrew R
Publicado em 2009

Postnatal Sim1 Deficiency Causes Hyperphagic Obesity and Reduced Mc4r and Oxytocin Expression

Por Tolson, Kristen P., Gemelli, Terry, Gautron, Laurent, Elmquist, Joel K., Zinn, Andrew R., Kublaoui, Bassil M.
Publicado em 2010

A Turner syndrome neurocognitive phenotype maps to Xp22.3

Por Elder Frederick F, Ramos Purita, Stefanatos Gerry, Roeltgen David, Zinn Andrew R, Kushner Harvey, Kowal Karen, Ross Judith L
Publicado em 2007-05-01

A Turner syndrome neurocognitive phenotype maps to Xp22.3

Por Zinn, Andrew R, Roeltgen, David, Stefanatos, Gerry, Ramos, Purita, Elder, Frederick F, Kushner, Harvey, Kowal, Karen, Ross, Judith L
Publicado em 2007

Behavioral and Social Phenotypes in Boys With 47,XYY Syndrome or 47,XXY Klinefelter Syndrome

Por Ross, Judith L., Roeltgen, David P., Kushner, Harvey, Zinn, Andrew R., Reiss, Allan, Bardsley, Martha Zeger, McCauley, Elizabeth, Tartaglia, Nicole
Publicado em 2012

Dynamic Regulation of p53 Subnuclear Localization and Senescence by MORC3

Por Takahashi, Keiko, Yoshida, Naofumi, Murakami, Naoko, Kawata, Kiyo, Ishizaki, Hiroyuki, Tanaka-Okamoto, Miki, Miyoshi, Jun, Zinn, Andrew R., Shime, Hiroaki, Inoue, Norimitsu
Publicado em 2007

A Serotonin and Melanocortin Circuit Mediates d-Fenfluramine Anorexia

Por Xu, Yong, Jones, Juli E., Lauzon, Danielle A., Anderson, Jason G., Balthasar, Nina, Heisler, Lora K., Zinn, Andrew R., Lowell, Bradford B., Elmquist, Joel K.
Publicado em 2010

DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13

Por Garcia, Nilda M., Allgood, Jocelyn, Santos, Lane J., Lonergan, D., Batanian, J.R., Henkemeyer, Mark, Bartsch, Oliver, Schultz, Roger A., Zinn, Andrew R., Baker, Linda A.
Publicado em 2006

Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse

Por Watson, Mark L., Zinn, Andrew R., Inoue, Norimitsu, Hess, Karl D., Cobb, John, Handel, Mary Ann, Halaban, Ruth, Duchene, Clark C., Albright, George M., Moreadith, Randall W.
Publicado em 1998

Screening and Familial Characterization of Copy-Number Variations in NR5A1 in 46,XY Disorders of Sex Development and Premature Ovarian Failure

Por Harrison, Steven M., Campbell, Ian M., Keays, Melise, Granberg, Candace F., Villanueva, Carlos, Tannin, Grace, Zinn, Andrew R., Castrillon, Diego H., Shaw, Chad A., Stankiewicz, Paweł, Baker, Linda A.
Publicado em 2013

Sequence variation at the human FOXO3 locus: A study of premature ovarian failure and primary amenorrhea

Por Gallardo, Teresa D., John, George B., Bradshaw, Karen, Welt, Corrine, Reijo-Pera, Renee, Vogt, Peter H., Touraine, Philippe, Bione, Silvia, Toniolo, Daniela, Nelson, Lawrence M., Zinn, Andrew R., Castrillon, Diego H.
Publicado em 2007

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

Por Bhoj, Elizabeth J, Ramos, Purita, Baker, Linda A, Cost, Nicholas, Nordenskjöld, Agneta, Elder, Frederick F, Bleyl, Steven B, Bowles, Neil E, Arrington, Cammon B, Delhomme, Brigitte, Vanhoutteghem, Amandine, Djian, Philippe, Zinn, Andrew R
Publicado em 2011