Research output per year
Research output per year
- 1 - 50 out of 121 results
Search results
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2023
A practical guide to graduate school interviewing for historically excluded individuals
Ransey, E., Brookens, S., Beasley, H. K., Marshall, A., Marlin, B. J., Rodriguez-Aliaga, P., Headley, C. A., Wanjalla, C., Vazquez, A. D., Murray, S., Damo, S., Taabazuing, C. Y. & Hinton, A., Jun 2023, In: American Journal of Physiology - Heart and Circulatory Physiology. 324, 6, p. H786-H790Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
2022
Using stakeholder insights to enhance engagement in PhD professional development
Ramadoss, D., Bolgioni, A. F., Layton, R. L., Alder, J., Lundsteen, N., Stayart, C. A., Yellin, J. B., Smart, C. L. & Varvayanis, S. S., Jan 2022, In: PloS one. 17, 1 January, e0262191.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
2019
NK cell defects in X-linked pigmentary reticulate disorder
Starokadomskyy, P., Wilton, K. M., Krzewski, K., Lopez, A., Sifuentes-Dominguez, L., Overlee, B., Chen, Q., Ray, A., Gil-Krzewska, A., Peterson, M., Kinch, L. N., Rohena, L., Grunebaum, E., Zinn, A. R., Grishin, N. V., Billadeau, D. D. & Burstein, E., Nov 1 2019, In: JCI Insight. 4, 21, e125688.Research output: Contribution to journal › Article › peer-review
Open Access16 Scopus citations -
Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression
Ross, J. L., Bloy, L., Roberts, T. P. L., Miller, J., Xing, C., Silverman, L. A. & Zinn, A. R., Oct 1 2019, In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 180, 7, p. 471-482 12 p.Research output: Contribution to journal › Article › peer-review
4 Scopus citations -
2018
Sex-chromosome dosage effects on gene expression in humans
Raznahan, A., Parikshak, N. N., Chandran, V., Blumenthal, J. D., Clasen, L. S., Alexander-Bloch, A. F., Zinn, A. R., Wangsa, D., Wise, J., Murphy, D. G. M., Bolton, P. F., Ried, T., Ross, J., Giedd, J. N. & Geschwind, D. H., Jul 10 2018, In: Proceedings of the National Academy of Sciences of the United States of America. 115, 28, p. 7398-7403 6 p.Research output: Contribution to journal › Article › peer-review
Open Access112 Scopus citations -
2017
Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region
Benito-Sanz, S., Belinchon-Martínez, A., Aza-Carmona, M., De La Torre, C., Huber, C., González-Casado, I., Ross, J. L., Thomas, N. S., Zinn, A. R., Cormier-Daire, V. & Heath, K. E., Feb 1 2017, In: Journal of Human Genetics. 62, 2, p. 229-234 6 p.Research output: Contribution to journal › Article › peer-review
9 Scopus citations -
The future of graduate and postdoctoral training in the biosciences
Hitchcock, P., Mathur, A., Bennett, J., Cameron, P., Chow, C., Clifford, P., Duvoisin, R., Feig, A., Finneran, K., Klotz, D. M., McGee, R., O’Riordan, M., Pfund, C., Pickett, C., Schwartz, N., Street, N. E., Watkins, E., Wiest, J. & Engelke, D., Oct 19 2017, In: eLife. 6, e32715.Research output: Contribution to journal › Article › peer-review
Open Access32 Scopus citations -
2016
DNA polymerase-α regulates the activation of type i interferons through cytosolic RNA:DNA synthesis
Starokadomskyy, P., Gemelli, T., Rios, J. J., Xing, C., Wang, R. C., Li, H., Pokatayev, V., Dozmorov, I., Khan, S., Miyata, N., Fraile, G., Raj, P., Xu, Z., Xu, Z., Ma, L., Lin, Z., Wang, H., Yang, Y., Ben-Amitai, D., Orenstein, N., & 11 others, May 1 2016, In: Nature immunology. 17, 5, p. 495-504 10 p.Research output: Contribution to journal › Article › peer-review
Open Access110 Scopus citations -
2015
Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features
Ross, J. L., Tartaglia, N., Merry, D. E., Dalva, M. & Zinn, A. R., Feb 1 2015, In: Genes, Brain and Behavior. 14, 2, p. 137-144 8 p.Research output: Contribution to journal › Article › peer-review
45 Scopus citations -
Sim1 inhibits bone formation by enhancing the sympathetic tone in male mice
Wang, X., Wei, W., Zinn, A. R. & Wan, Y., Apr 1 2015, In: Endocrinology. 156, 4, p. 1408-1415 8 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
2014
Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia.
Heymsfield, S. B., Avena, N. M., Baier, L., Brantley, P., Bray, G. A., Burnett, L. C., Butler, M. G., Driscoll, D. J., Egli, D., Elmquist, J., Forster, J. L., Goldstone, A. P., Gourash, L. M., Greenway, F. L., Han, J. C., Kane, J. G., Leibel, R. L., Loos, R. J. F., Scheimann, A. O., Roth, C. L., & 9 others, Feb 2014, In: Obesity (Silver Spring, Md.). 22 Suppl 1, p. S1-S17Research output: Contribution to journal › Article › peer-review
Open Access70 Scopus citations -
Inducible neuronal inactivation of Sim1 in adult mice causes hyperphagic obesity
Tolson, K. P., Gemelli, T., Meyer, D., Yazdani, U., Kozlitina, J. & Zinn, A. R., Jul 2014, In: Endocrinology. 155, 7, p. 2436-2444 9 p.Research output: Contribution to journal › Article › peer-review
23 Scopus citations -
2013
Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure
Harrison, S. M., Campbell, I. M., Keays, M., Granberg, C. F., Villanueva, C., Tannin, G., Zinn, A. R., Castrillon, D. H., Shaw, C. A., Stankiewicz, P. & Baker, L. A., Oct 2013, In: American Journal of Medical Genetics, Part A. 161, 10, p. 2487-2494 8 p.Research output: Contribution to journal › Article › peer-review
Open Access25 Scopus citations -
2012
Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY klinefelter syndrome
Ross, J. L., Roeltgen, D. P., Kushner, H., Zinn, A. R., Reiss, A., Bardsley, M. Z., McCauley, E. & Tartaglia, N., Apr 2012, In: Pediatrics. 129, 4, p. 769-778 10 p.Research output: Contribution to journal › Article › peer-review
Open Access135 Scopus citations -
Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome
Payne, A. R., Chang, S. W., Koenig, S. N., Zinn, A. R. & Garg, V., Jun 2012, In: Pediatric Cardiology. 33, 5, p. 757-763 7 p.Research output: Contribution to journal › Article › peer-review
36 Scopus citations -
2011
Clinical and molecular evaluation of SHOX/PAR1 duplications in léri-weill dyschondrosteosis (LWD) and idiopathic short stature (ISS)
Benito-Sanz, S., Barroso, E., Heine-Suñer, D., Hisado-Oliva, A., Romanelli, V., Rosell, J., Aragones, A., Caimari, M., Argente, J., Ross, J. L., Zinn, A. R., Gracia, R., Lapunzina, P., Campos-Barros, A. & Heath, K. E., Feb 2011, In: Journal of Clinical Endocrinology and Metabolism. 96, 2, p. E404-E412Research output: Contribution to journal › Article › peer-review
58 Scopus citations -
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development
Bhoj, E. J., Ramos, P., Baker, L. A., Cost, N., Nordenskjöld, A., Elder, F. F., Bleyl, S. B., Bowles, N. E., Arrington, C. B., Delhomme, B., Vanhoutteghem, A., Djian, P. & Zinn, A. R., May 2011, In: European Journal of Human Genetics. 19, 5, p. 540-546 7 p.Research output: Contribution to journal › Article › peer-review
22 Scopus citations -
2010
A serotonin and melanocortin circuit mediates D-fenfluramine anorexia
Xu, Y., Jones, J. E., Lauzon, D. A., Anderson, J. G., Balthasar, N., Heisler, L. K., Zinn, A. R., Lowell, B. B. & Elmquist, J. K., Nov 3 2010, In: Journal of Neuroscience. 30, 44, p. 14630-14634 5 p.Research output: Contribution to journal › Article › peer-review
74 Scopus citations -
Distribution and neurochemical characterization of protein kinase C-theta and -delta in the rodent hypothalamus
Irani, B. G., Donato, J., Olson, D. P., Lowell, B. B., Sacktor, T. C., Reyland, M. E., Tolson, K. P., Zinn, A. R., Ueta, Y., Sakata, I., Zigman, J. M., Elias, C. F. & Clegg, D. J., Nov 2010, In: Neuroscience. 170, 4, p. 1065-1079 15 p.Research output: Contribution to journal › Article › peer-review
22 Scopus citations -
Postnatal Sim1 deficiency causes hyperphagic obesity and reduced Mc4r and oxytocin expression
Tolson, K. P., Gemelli, T., Gautron, L., Elmquist, J. K., Zinn, A. R. & Kublaoui, B. M., Mar 10 2010, In: Journal of Neuroscience. 30, 10, p. 3803-3812 10 p.Research output: Contribution to journal › Article › peer-review
113 Scopus citations -
UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients
De Leeuw, N., Bulk, S., Green, A., Jaeckle-Santos, L., Baker, L. A., Zinn, A. R., Kleefstra, T., Van Der Smagt, J. J., Vianne Morgante, A. M., De Vries, B. B. A., Van Bokhoven, H. & De Brouwer, A. P. M., Dec 2010, In: American Journal of Medical Genetics, Part A. 152 A, 12, p. 3084-3090 7 p.Research output: Contribution to journal › Article › peer-review
31 Scopus citations -
Unconventional wisdom about the obesity epidemic
Zinn, A. R., Dec 2010, In: American Journal of the Medical Sciences. 340, 6, p. 481-491 11 p.Research output: Contribution to journal › Article › peer-review
12 Scopus citations -
2009
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
Ross, J. L., Zeger, M. P. D., Kushner, H., Zinn, A. R. & Roeltgen, D. P., 2009, In: Developmental Disabilities Research Reviews. 15, 4, p. 309-317 9 p.Research output: Contribution to journal › Article › peer-review
Open Access100 Scopus citations -
Computing power of quantitative trait locus association mapping for haploid loci
Gordon, D. & Zinn, A. R., Aug 23 2009, In: BMC Bioinformatics. 10, 261.Research output: Contribution to journal › Article › peer-review
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Effect of growth hormone therapy on severe short stature and skeletal deformities in a patient with combined turner syndrome and langer mesomelic dysplasia
Shah, B. C., Moran, E. S., Zinn, A. R. & Pappas, J. G., Dec 2009, In: Journal of Clinical Endocrinology and Metabolism. 94, 12, p. 5028-5033 6 p.Research output: Contribution to journal › Article › peer-review
6 Scopus citations -
MODY-like diabetes associated with an apparently balanced translocation: Possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes
Bhoj, E. J., Romeo, S., Baroni, M. G., Bartov, G., Schultz, R. A. & Zinn, A. R., 2009, In: Molecular Cytogenetics. 2, 1, 5.Research output: Contribution to journal › Article › peer-review
8 Scopus citations -
2008
Cognitive and motor development during childhood in boys with Klinefelter syndrome
Ross, J. L., Roeltgen, D. P., Stefanatos, G., Benecke, R., Zeger, M. P. D., Kushner, H., Ramos, P., Elder, F. F. & Zinn, A. R., Mar 15 2008, In: American Journal of Medical Genetics, Part A. 146, 6, p. 708-719 12 p.Research output: Contribution to journal › Article › peer-review
152 Scopus citations -
Cryptic chromosomal abnormalities identified in children with congenital heart disease
Richards, A. A., Santos, L. J., Nichols, H. A., Crider, B. P., Elder, F. F., Hauser, N. S., Zinn, A. R. & Garg, V., Oct 2008, In: Pediatric Research. 64, 4, p. 358-363 6 p.Research output: Contribution to journal › Article › peer-review
85 Scopus citations -
Effect of Ascertainment and Genetic Features on the Phenotype of Klinefelter Syndrome
Zeger, M. P. D., Zinn, A. R., Lahlou, N., Ramos, P., Kowal, K., Samango-Sprouse, C. & Ross, J. L., May 2008, In: Journal of Pediatrics. 152, 5, p. 716-722 7 p.Research output: Contribution to journal › Article › peer-review
87 Scopus citations -
EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome
Zinn, A. R., Kushner, H. & Ross, J. L., Jun 5 2008, In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147, 4, p. 507-509 3 p.Research output: Contribution to journal › Article › peer-review
9 Scopus citations -
Oxytocin deficiency mediates hyperphagic obesity of Sim1 haploinsufficient mice
Kublaoui, B. M., Gemelli, T., Tolson, K. P., Wang, Y. & Zinn, A. R., Jul 2008, In: Molecular Endocrinology. 22, 7, p. 1723-1734 12 p.Research output: Contribution to journal › Article › peer-review
201 Scopus citations -
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes
Jaeckle Santos, L. J., Xing, C., Barnes, R. B., Ades, L. C., Megarbane, A., Vidal, C., Xuereb, A., Tarpey, P. S., Smith, R., Khazab, M., Shoubridge, C., Partington, M., Futreal, A., Stratton, M. R., Gecz, J. & Zinn, A. R., Jun 2008, In: Human genetics. 123, 5, p. 469-476 8 p.Research output: Contribution to journal › Article › peer-review
Open Access16 Scopus citations -
Sequence variation at the human FOXO3 locus: A study of premature ovarian failure and primary amenorrhea
Gallardo, T. D., John, G. B., Bradshaw, K., Welt, C., Reijo-Pera, R., Vogt, P. H., Touraine, P., Bione, S., Toniolo, D., Nelson, L. M., Zinn, A. R. & Castrillon, D. H., Jan 2008, In: Human Reproduction. 23, 1, p. 216-221 6 p.Research output: Contribution to journal › Article › peer-review
44 Scopus citations -
2007
A turner syndrome neurocognitive phenotype maps to Xp22.3
Zinn, A. R., Roeltgen, D., Stefanatos, G., Ramos, P., Elder, F. F., Kushner, H., Kowal, K. & Ross, J. L., May 21 2007, In: Behavioral and Brain Functions. 3, 24.Research output: Contribution to journal › Article › peer-review
62 Scopus citations -
Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD)
Campos-Barros, Á., Benito-Sanz, S., Ross, J. L., Zinn, A. R. & Heath, K. E., May 1 2007, In: American Journal of Medical Genetics, Part A. 143, 9, p. 933-938 6 p.Research output: Contribution to journal › Article › peer-review
19 Scopus citations -
Dynamic regulation of p53 subnuclear localization and senescence by MORC3
Takahashi, K., Yoshida, N., Murakami, N., Kawata, K., Ishizaki, H., Tanaka-Okamoto, M., Miyoshi, J., Zinn, A. R., Shime, H. & Inoue, N., May 2007, In: Molecular biology of the cell. 18, 5, p. 1701-1709 9 p.Research output: Contribution to journal › Article › peer-review
Open Access74 Scopus citations -
Mutational analyses of UPIIIA, SHH, EFNB2, and HNF1β in persistent cloaca and associated kidney malformations
Jenkins, D., Bitner-Glindzicz, M., Thomasson, L., Malcolm, S., Warne, S. A., Feather, S. A., Flanagan, S. E., Ellard, S., Bingham, C., Santos, L., Henkemeyer, M., Zinn, A., Baker, L. A., Wilcox, D. T. & Woolf, A. S., Feb 2007, In: Journal of Pediatric Urology. 3, 1, p. 2-9 8 p.Research output: Contribution to journal › Article › peer-review
Open Access26 Scopus citations -
Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease
Prieto, J. C., Garcia, N. M., Elder, F. F., Zinn, A. R. & Baker, L. A., Nov 2007, In: Journal of Pediatric Surgery. 42, 11, p. 1928-1932 5 p.Research output: Contribution to journal › Article › peer-review
21 Scopus citations -
The physical phenotype of girls and women with Turner syndrome is not X-imprinted
Bondy, C. A., Matura, L. A., Wooten, N., Troendle, J., Zinn, A. R. & Bakalov, V. K., May 2007, In: Human genetics. 121, 3-4, p. 469-474 6 p.Research output: Contribution to journal › Article › peer-review
33 Scopus citations -
2006
Deletion mapping of critical region for hypospadias, penoscrotal transposition and imperforate anus on human chromosome 13
Garcia, N. M., Allgood, J., Santos, L. J., Lonergan, D., Batanian, J. R., Dravis, C., Henkemeyer, M., Bartsch, O., Schultz, R. A., Zinn, A. R. & Baker, L. A., Aug 2006, In: Journal of Pediatric Urology. 2, 4, p. 233-242 10 p.Research output: Contribution to journal › Article › peer-review
33 Scopus citations -
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects
Russell, H. F., Wallis, D., Mazzocco, M. M. M., Moshang, T., Zackai, E., Zinn, A. R., Ross, J. L. & Muenke, M., Oct 2006, In: Journal of pediatric psychology. 31, 9, p. 945-955 11 p.Research output: Contribution to journal › Article › peer-review
98 Scopus citations -
Sim1 haploinsufficiency impairs melanocortin-mediated anorexia and activation of paraventricular nucleus neurons
Kublaoui, B. M., Holder, J. L., Gemelli, T. & Zinn, A. R., 2006, In: Molecular Endocrinology. 20, 10, p. 2483-2492 10 p.Research output: Contribution to journal › Article › peer-review
100 Scopus citations -
SIM1 overexpression partially rescues agouti yellow and diet-induced obesity by normalizing food intake
Kublaoui, B. M., Holder, J. L., Tolson, K. P., Gemelli, T. & Zinn, A. R., 2006, In: Endocrinology. 147, 10, p. 4542-4549 8 p.Research output: Contribution to journal › Article › peer-review
62 Scopus citations -
2005
Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome
Zinn, A. R., Ramos, P., Elder, F. F., Kowal, K., Samango-Sprouse, C. & Ross, J. L., Sep 2005, In: Journal of Clinical Endocrinology and Metabolism. 90, 9, p. 5041-5046 6 p.Research output: Contribution to journal › Article › peer-review
107 Scopus citations -
Distinct roles for the mammalian A-type cyclins during oogenesis
Persson, J. L., Zhang, Q., Wang, X. Y., Ravnik, S. E., Muhlrad, S. & Wolgemuth, D. J., Oct 2005, In: Reproduction. 130, 4, p. 411-422 12 p.Research output: Contribution to journal › Article › peer-review
24 Scopus citations -
Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome
Ross, J. L., Samango-Sprouse, C., Lahlou, N., Kowal, K., Elder, F. F. & Zinn, A., Sep 2005, In: Hormone Research. 64, 1, p. 39-45 7 p.Research output: Contribution to journal › Article › peer-review
128 Scopus citations -
The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: Contrasting children with Leri-Weill dyschondrosteosis and turner syndrome
Ross, J. L., Kowal, K., Quigley, C. A., Blum, W. F., Cutler, G. B., Crowe, B., Hovanes, K., Elder, F. F. & Zinn, A. R., Oct 2005, In: Journal of Pediatrics. 147, 4, p. 499-507 9 p.Research output: Contribution to journal › Article › peer-review
71 Scopus citations -
2004
Sim1 gene dosage modulates the homeostatic feeding response to increased dietary fat in mice
Holder, J. L., Zhang, L., Kublaoui, B. M., DiLeone, R. J., Oz, O. K., Bair, C. H., Lee, Y. H. & Zinn, A. R., Jul 2004, In: American Journal of Physiology - Endocrinology and Metabolism. 287, 1 50-1, p. E105-E113Research output: Contribution to journal › Article › peer-review
73 Scopus citations -
The effect of genetic differences and ovarian failure: Intact cognitive function in adult women with premature ovarian failure versus turner syndrome
Ross, J. L., Stefanatos, G. A., Kushner, H., Bondy, C., Nelson, L., Zinn, A. & Roeltgen, D., Apr 2004, In: Journal of Clinical Endocrinology and Metabolism. 89, 4, p. 1817-1822 6 p.Research output: Contribution to journal › Article › peer-review
53 Scopus citations -
2003
Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasia
Ross, J. L., Bellus, G., Scott, C. I., Abboudi, J., Grigelioniene, G. & Zinn, A. R., Jan 1 2003, In: American Journal of Medical Genetics. 116, 1, p. 61-65 5 p.Research output: Contribution to journal › Article › peer-review
14 Scopus citations