Stanley Nelson, M.D.


snelson@ucla.edu


Laboratory Address:
Lab
5554 Gonda

UNITED STATES

Work Address:
Office
UCLA Hum Genetics
BOX 957088
5506A Gonda Cntr
Los Angeles, CA 90095
UNITED STATES


Detailed profile
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Quick Links Semel Institute for Neuroscience and Human Behavior at UCLA Resnick Neuropsychiatric Hospital Department of Psychiatry and Biobehavioral Sciences
Bio:

Stanley F. Nelson, MD is Professor and Vice Chair of Human Genetics and Professor of Psychiatry within the David Geffen School of Medicine at UCLA where he has been on faculty since 1993. Prof. Nelson attended the University of Michigan and obtained a BS degree in Physics in 1982. He graduated from Duke University School of Medicine in 1987 and completed an ITT International Fellowship to Sweden in the Laboratory of George Klein. He was trained in Pediatrics and Pediatric Hematology-Oncology at UCSF School of Medicine, and subsequently trained as a postdoctoral fellow with Patrick Brown from 1990-1993 where he developed genomic mismatch scanning and initiated the lab development of DNA microarrays for genomic applications. At UCLA, Prof. Nelson has continued to be interested in technology development and application of genomics to cancer biology and common human diseases with active research areas in Autism, ADHD, vertigo and brain cancers. He developed and continues to direct the UCLA DNA Microarray Facility which provides access to whole genome expression array analysis for faculty on campus and for the NIH Neuroscience Blueprint. His current interest is in the development and application of technologies for whole genome sequencing and cancer genome sequencing.


Publications:

Lu Steven E, Ogdie Steven E, Jarvelin Steven E, Moilanen Steven E, Loo Steven E, McCracken Steven E, McGough Steven E, Yang Steven E, Peltonen Steven E, Nelson Steven E, Cantor Steven E, Smalley Steven E Association of the cannabinoid receptor gene (CNR1) with ADHD and post-traumatic stress disorder.. Am. J. Med. Genet. B Neuropsychiatr. Genet.. 2008; 452(7184): .
Rock, Prenen, Funari, Funari, Merriman, Nelson, Lachman, Wilcox, Reyno, Quadrelli, Vaglio, Owsianik, Janssens, Voets, Ikegawa, Nagai, Rimoin, Nilius, Cohn Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.. Nat. Genet.. 2008; .
Sivagnanam, Mueller, Lee, Chen, Nelson, Turner, Zlotkin, Pencharz, Ngan, Libiger, Schork, Lavine, Taylor, Newbury, Kolodner, Hoffman Identification of EpCAM as the Gene for Congenital Tufting Enteropathy.. Gastroenterology. 2008; .
Alarcon Maricela, Abrahams Brett S, Stone Jennifer L, Duvall Jacqueline A, Perederiy Julia V, Bomar Jamee M, Sebat Jonathan, Wigler Michael, Martin Christa L, Ledbetter David H, Nelson Stanley F, Cantor Rita M, Geschwind Daniel H Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.. Am. J. Hum. Genet.. 2008; 82(1): 150-9.
Nakano Ichiro, Masterman-Smith Michael, Saigusa Kuniyasu, Paucar Andres A, Horvath Steve, Shoemaker Lorelei, Watanabe Momoko, Negro Alejandra, Bajpai Ruchi, Howes Amy, Lelievre Vincent, Waschek James A, Lazareff Jorge A, Freije William A, Liau Linda M, Gilbertson Richard J, Cloughesy Timothy F, Geschwind Daniel H, Nelson Stanley F, Mischel Paul S, Terskikh Alexey V, Kornblum Harley I Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells.. J. Neurosci. Res.. 2008; 86(1): 48-60.
Walsh Tom, McClellan Jon M, McCarthy Shane E, Addington AM, Pierce Sarah B, Cooper Greg M, Nord Alex S, Kusenda Mary, Malhotra Dheeraj, Bhandari Abhishek, Stray Sunday M, Rippey Caitlin F, Roccanova Patricia, Makarov Vlad, Lakshmi B, Findling Robert L, Sikich Linmarie, Stromberg Thomas, Merriman Barry, Gogtay Nitin, Butler Philip, Eckstrand Kristen, Noory Laila, Gochman Peter, Long Robert, Chen Zugen, Davis Sean, Baker Carl, Eichler Evan E, Meltzer Paul S, Nelson Stanley F, Singleton Andrew B, Lee Ming K, Rapoport Judith L, King Mary-Claire, Sebat Jonathan Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.. Science. 2008; 320(5875): 539-43.
Stanczak Christopher M, Chen Zugen, Nelson Stanley F, Suchard Marc, McCabe Edward R B, McGhee Sean Representational oligonucleotide microarray analysis (ROMA) and comparison of binning and change-point methods of analysis: application to detection of del22q11.2 (DiGeorge) syndrome.. Hum. Mutat.. 2008; 29(1): 176-81.
Cokus Shawn J, Feng Suhua, Zhang Xiaoyu, Chen Zugen, Merriman Barry, Haudenschild Christian D, Pradhan Sriharsa, Nelson Stanley F, Pellegrini Matteo, Jacobsen Steven E Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning.. Nature. 2008; 452(7184): 215-9.
Kerber Kevin A, Jen Joanna C, Lee Hane, Nelson Stanley F, Baloh Robert W A new episodic ataxia syndrome with linkage to chromosome 19q13.. Arch. Neurol.. 2007; 64(5): 749-52.
Nyman Emma S, Ogdie Matthew N, Loukola Anu, Varilo Teppo, Taanila Anja, Hurtig Tuula, Moilanen Irma K, Loo Sandra K, McGough James J, Jorvelin Marjo-Riitta, Smalley Susan L, Nelson Stanley F, Peltonen Leena ADHD candidate gene study in a population-based birth cohort: association with DBH and DRD2.. J. Neurosci. Res.. 2007; 46(12): 1614-21.
Lee Hane, Sininger Lauren, Jen Joanna C, Cha Yoon-Hee, Baloh Robert W, Nelson Stanley F Association of progesterone receptor with migraine-associated vertigo.. Neurogenetics. 2007; 8(3): 195-200.
Richards Anna, van den Maagdenberg Arn M J M, Jen Joanna C, Kavanagh David, Bertram Paula, Spitzer Dirk, Liszewski M Kathryn, Barilla-Labarca Maria-Louise, Terwindt Gisela M, Kasai Yumi, McLellan Mike, Grand Mark Gilbert, Vanmolkot Kaate R J, de Vries Boukje, Wan Jijun, Kane Michael J, Mamsa Hafsa, Sch����fer Ruth, Stam Anine H, Haan Joost, de Jong Paulus T V M, Storimans Caroline W, van Schooneveld Mary J, Oosterhuis Jendo A, Gschwendter Andreas, Dichgans Martin, Kotschet Katya E, Hodgkinson Suzanne, Hardy Todd A, Delatycki Martin B, Hajj-Ali Rula A, Kothari Parul H, Nelson Stanley F, Frants Rune R, Baloh Robert W, Ferrari Michel D, Atkinson John P C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.. Nat. Genet.. 2007; 39(9): 1068-70.
Funari Vincent A, Day Allen, Krakow Deborah, Cohn Zachary A, Chen Zugen, Nelson Stanley F, Cohn Daniel H Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression.. BMC Genomics. 2007; 8(3): 165.
Day Allen, Carlson Marc R J, Dong Jun, O'Connor Brian D, Nelson Stanley F Celsius: a community resource for Affymetrix microarray data.. Genome Biol.. 2007; 8(6): R112.
Stanczak Christopher M, Chen Zugen, Zhang Yao-Hua, Nelson Stanley F, McCabe Edward R B Deletion mapping in Xp21 for patients with complex glycerol kinase deficiency using SNP mapping arrays.. Hum. Mutat.. 2007; 28(3): 235-42.
Liu Tsunglin, Papagiannakopoulos Thales, Puskar Kathy, Qi Shuping, Santiago Fernando, Clay William, Lao Kaiqin, Lee Yohan, Nelson Stanley F, Kornblum Harley I, Doyle Frank, Petzold Linda, Shraiman Boris, Kosik Kenneth S Detection of a microRNA signal in an in vivo expression set of mRNAs.. PLoS ONE. 2007; 2(8): e804.
Stone Jennifer L, Merriman Barry, Cantor Rita M, Geschwind Daniel H, Nelson Stanley F High density SNP association study of a major autism linkage region on chromosome 17.. Hum. Mol. Genet.. 2007; 16(6): 704-15.
Dwyer Jennifer R, Sever Navdar, Carlson Marc, Nelson Stanley F, Beachy Philip A, Parhami Farhad Oxysterols are novel activators of the hedgehog signaling pathway in pluripotent mesenchymal cells.. J. Biol. Chem.. 2007; 282(12): 8959-68.
Lee Harley I, Jen Harley I, Cha Harley I, Nelson Harley I, Baloh Harley I Phenotypic and Genetic Analysis of a Large Family With Migraine-Associated Vertigo.. J. Neurosci. Res.. 2007; 86(1): .
Smalley Susan L, McGough James J, Moilanen Irma K, Loo Sandra K, Taanila Anja, Ebeling Hanna, Hurtig Tuula, Kaakinen Marika, Humphrey Lorie A, McCracken James T, Varilo Teppo, Yang May H, Nelson Stanley F, Peltonen Leena, Jarvelin Marjo-Riitta Prevalence and psychiatric comorbidity of attention-deficit/hyperactivity disorder in an adolescent Finnish population.. J. Neurosci. Res.. 2007; 46(12): 1575-83.
Carlson Marc R J, Pope Whitney B, Horvath Steve, Braunstein Jerome G, Nghiemphu Phioanh, Tso Cho-Lea, Mellinghoff Ingo, Lai Albert, Liau Linda M, Mischel Paul S, Dong Jun, Nelson Stanley F, Cloughesy Timothy F Relationship between survival and edema in malignant gliomas: role of vascular endothelial growth factor and neuronal pentraxin 2.. Clin. Cancer Res.. 2007; 13(9): 2592-8.
Nikolova Ganka, Lee Hane, Berkovitz Suzanne, Nelson Stanley, Sinsheimer Janet, Vilain Eric, Rodr����guez Larissa V Sequence variant in the laminin gamma1 (LAMC1) gene associated with familial pelvic organ prolapse.. Hum. Genet.. 2007; 120(6): 847-56.
Lee Hane, Jen Joanna C, Wang Hui, Chen Zugen, Mamsa Hafsa, Sabatti Chiara, Baloh Robert W, Nelson Stanley F A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.. Hum. Mol. Genet.. 2006; 15(2): 251-8.
Lacombe Arnaud, Lee Hane, Zahed Laila, Choucair Mahmoud, Muller Jean-Marc, Nelson Stanley F, Salameh Wael, Vilain Eric Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.. Am. J. Hum. Genet.. 2006; 79(1): 113-9.
Mitchell Scherise, Ota Asuka, Foster William, Zhang Bin, Fang Zixing, Patel Shilpa, Nelson Stanley F, Horvath Steve, Wang Yibin Distinct gene expression profiles in adult mouse heart following targeted MAP kinase activation.. Physiol. Genomics. 2006; 25(1): 50-9.
Tso Cho-Lea, Freije William A, Day Allen, Chen Zugen, Merriman Barry, Perlina Ally, Lee Yohan, Dia Ederlyn Q, Yoshimoto Koji, Mischel Paul S, Liau Linda M, Cloughesy Timothy F, Nelson Stanley F Distinct transcription profiles of primary and secondary glioblastoma subgroups.. Cancer Res.. 2006; 66(1): 159-67.
Lee Jeffrey C, Vivanco Igor, Beroukhim Rameen, Huang Julie H Y, Feng Whei L, DeBiasi Ralph M, Yoshimoto Koji, King Jennifer C, Nghiemphu Phioanh, Yuza Yuki, Xu Qing, Greulich Heidi, Thomas Roman K, Paez J Guillermo, Peck Timothy C, Linhart David J, Glatt Karen A, Getz Gad, Onofrio Robert, Ziaugra Liuda, Levine Ross L, Gabriel Stacey, Kawaguchi Tomohiro, O'Neill Keith, Khan Haumith, Liau Linda M, Nelson Stanley F, Rao P Nagesh, Mischel Paul, Pieper Russell O, Cloughesy Tim, Leahy Daniel J, Sellers William R, Sawyers Charles L, Meyerson Matthew, Mellinghoff Ingo K Epidermal growth factor receptor activation in glioblastoma through novel missense mutations in the extracellular domain.. PLoS Med.. 2006; 3(12): e485.
Lee Hans, Zhang Yanqiao, Lee Florence Y, Nelson Stanley F, Gonzalez Frank J, Edwards Peter A FXR regulates organic solute transporters alpha and beta in the adrenal gland, kidney, and intestine.. J. Lipid Res.. 2006; 47(1): 201-14.
Carlson Marc R J, Zhang Bin, Fang Zixing, Mischel Paul S, Horvath Steve, Nelson Stanley F Gene connectivity, function, and sequence conservation: predictions from modular yeast co-expression networks.. BMC Genomics. 2006; 7(1): 40.
Gargalovic Peter S, Imura Minori, Zhang Bin, Gharavi Nima M, Clark Michael J, Pagnon Joanne, Yang Wen-Pin, He Aiqing, Truong Amy, Patel Shilpa, Nelson Stanley F, Horvath Steve, Berliner Judith A, Kirchgessner Todd G, Lusis Aldons J Identification of inflammatory gene modules based on variations of human endothelial cell responses to oxidized lipids.. Proc. Natl. Acad. Sci. U.S.A.. 2006; 103(34): 12741-6.
Tso Cho-Lea, Shintaku Peter, Chen James, Liu Qinghai, Liu Jason, Chen Zugen, Yoshimoto Koji, Mischel Paul S, Cloughesy Timothy F, Liau Linda M, Nelson Stanley F Primary glioblastomas express mesenchymal stem-like properties.. Mol. Cancer Res.. 2006; 4(9): 607-19.
Todd Richard D, Huang Hongyan, Smalley Susan L, Nelson Stanley F, Willcutt Erik G, Pennington Bruce F, Smith Shelley D, Faraone Stephen V, Neuman Rosalind J Collaborative analysis of DRD4 and DAT genotypes in population-defined ADHD subtypes.. Invest. Ophthalmol. Vis. Sci.. 2005; 46(10): 1067-73.
Lu Kan V, Jong Kimberly A, Kim Gloria Y, Singh Jatinder, Dia Ederlyn Q, Yoshimoto Koji, Wang Maria Y, Cloughesy Timothy F, Nelson Stanley F, Mischel Paul S Differential induction of glioblastoma migration and growth by two forms of pleiotrophin.. J. Biol. Chem.. 2005; 280(29): 26953-64.
Shen D, Chang HR, Chen Z, He J, Lonsberry V, Elshimali Y, Chia D, Seligson D, Goodglick L, Nelson SF, Gornbein JA Loss of annexin A1 expression in human breast cancer detected by multiple high-throughput analyses.. Biochemical and biophysical research communications. . 2005; 326(1): 218-27.
Shen Dejun, Chang Helena R, Chen Zugen, He Jianbo, Lonsberry Victor, Elshimali Yahya, Chia David, Seligson David, Goodglick Lee, Nelson Stanley F, Gornbein Jeffrey A Loss of annexin A1 expression in human breast cancer detected by multiple high-throughput analyses.. Biochem. Biophys. Res. Commun.. 2005; 326(1): 218-27.
Nakano Ichiro, Paucar Andres A, Bajpai Ruchi, Dougherty Joseph D, Zewail Amani, Kelly Theresa K, Kim Kevin J, Ou Jing, Groszer Matthias, Imura Tetsuya, Freije William A, Nelson Stanley F, Sofroniew Michael V, Wu Hong, Liu Xin, Terskikh Alexey V, Geschwind Daniel H, Kornblum Harley I Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferation.. J. Cell Biol.. 2005; 170(3): 413-27.
Saghizadeh Mehrnoosh, Kramerov Andrei A, Tajbakhsh Jian, Aoki Annette M, Wang Charles, Chai Ning-Ning, Ljubimova Julia Y, Sasaki Takako, Sosne Gabriel, Carlson Marc R J, Nelson Stanley F, Ljubimov Alexander V Proteinase and growth factor alterations revealed by gene microarray analysis of human diabetic corneas.. Invest. Ophthalmol. Vis. Sci.. 2005; 46(10): 3604-15.
Cantor Rita M, Kono Naoko, Duvall Jackie A, Alvarez-Retuerto Ana, Stone Jennifer L, Alarc����n Maricela, Nelson Stanley F, Geschwind Daniel H Replication of autism linkage: fine-mapping peak at 17q21.. Am. J. Hum. Genet.. 2005; 76(6): 1050-6.
Mehrian Shai Ruty, Reichardt Juergen K V, Ya-Hsuan Hsu, Kremen Thomas J, Liau Linda M, Cloughesy Timothy F, Mischel Paul S, Nelson Stanley F Robustness of gene expression profiling in glioma specimen samplings and derived cell lines.. Brain Res. Mol. Brain Res.. 2005; 136(1-2): 99-103.
Lynn Deborah E, Lubke Gitta, Yang May, McCracken James T, McGough James J, Ishii Janeen, Loo Sandra K, Nelson Stanley F, Smalley Susan L Temperament and character profiles and the dopamine D4 receptor gene in ADHD.. Brain Res. Mol. Brain Res.. 2005; 162(5): 906-13.
Lee Hane, Wang Hui, Jen Joanna C, Sabatti Chiara, Baloh Robert W, Nelson Stanley F A novel mutation in KCNA1 causes episodic ataxia without myokymia.. Hum. Mutat.. 2004; 24(6): 536.
Ogdie Matthew N, Fisher Simon E, Yang May, Ishii Janeen, Francks Clyde, Loo Sandra K, Cantor Rita M, McCracken James T, McGough James J, Smalley Susan L, Nelson Stanley F Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.. Am. J. Hum. Genet.. 2004; 75(4): 661-8.
Mischel Paul S, Cloughesy Timothy F, Nelson Stanley F DNA-microarray analysis of brain cancer: molecular classification for therapy.. Nat. Rev. Neurosci.. 2004; 5(10): 782-92.
Mischel PS, Cloughesy TF, Nelson SF DNA-microarray analysis of brain cancer: molecular classification for therapy.. Nature reviews. Neuroscience. . 2004; 5(10): 782-92.
Le K, Mitsouras K, Roy M, Wang Q, Xu Q, Nelson SF, Lee C Detecting tissue-specific regulation of alternative splicing as a qualitative change in microarray data. Nucleic Acids Res. 2004; 32(22): e180.
Le Keith, Mitsouras Katherine, Roy Meenakshi, Wang Qi, Xu Qiang, Nelson Stanley F, Lee Christopher Detecting tissue-specific regulation of alternative splicing as a qualitative change in microarray data.. Nucleic Acids Res.. 2004; 32(22): e180.
Stone Jennifer L, Merriman Barry, Cantor Rita M, Yonan Amanda L, Gilliam T Conrad, Geschwind Daniel H, Nelson Stanley F Evidence for sex-specific risk alleles in autism spectrum disorder.. Am. J. Hum. Genet.. 2004; 75(6): 1117-23.
Freije William A, Castro-Vargas F Edmundo, Fang Zixing, Horvath Steve, Cloughesy Timothy, Liau Linda M, Mischel Paul S, Nelson Stanley F Gene expression profiling of gliomas strongly predicts survival.. Cancer Res.. 2004; 64(18): 6503-10.
Jen Joanna C, Chan Wai-Man, Bosley Thomas M, Wan Jijun, Carr Janai R, R����b Udo, Shattuck David, Salamon Georges, Kudo Lili C, Ou Jing, Lin Doris D M, Salih Mustafa A M, Kansu T����lay, Al Dhalaan Hesham, Al Zayed Zayed, MacDonald David B, Stigsby Bent, Plaitakis Andreas, Dretakis Emmanuel K, Gottlob Irene, Pieh Christina, Traboulsi Elias I, Wang Qing, Wang Lejin, Andrews Caroline, Yamada Koki, Demer Joseph L, Karim Shaheen, Alger Jeffry R, Geschwind Daniel H, Deller Thomas, Sicotte Nancy L, Nelson Stanley F, Baloh Robert W, Engle Elizabeth C Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.. Science. 2004; 304(5676): 1509-13.
Molina Omar Franklin, dos Santos Jos����, Nelson Stanley, Nowlin Thomas, Mazzetto Marcelo A clinical comparison of internal joint disorders in patients presenting disk-attachment pain: prevalence, characterization, and severity of bruxing behavior.. Biomol. Eng.. 2003; 21(1): 17-23.
Ogdie Matthew N, Macphie I Laurence, Minassian Sonia L, Yang May, Fisher Simon E, Francks Clyde, Cantor Rita M, McCracken James T, McGough James J, Nelson Stanley F, Monaco Anthony P, Smalley Susan L A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.. Am. J. Hum. Genet.. 2003; 72(5): 1268-79.
dos Santos Jose, Nelson Stanley, Nowlin Thomas Comparison of condylar guidance setting obtained from a wax record versus an extraoral tracing: a pilot study.. Biomol. Eng.. 2003; 89(1): 54-9.
Saghizadeh Mehrnoosh, Brown Donald J, Tajbakhsh Jian, Chen Zugen, Kenney M Cristina, Farber Debora B, Nelson Stanley F Evaluation of techniques using amplified nucleic acid probes for gene expression profiling.. Biomol. Eng.. 2003; 20(3): 97-106.
Saghizadeh M, Brown DJ, Tajbakhsh J, Chen Z, Kenney MC, Farber DB, Nelson SF Evaluation of techniques using amplified nucleic acid probes for gene expression profiling. Biomol Eng. 2003; 20(3): 97-106.
Shai Ruty, Shi Tao, Kremen Thomas J, Horvath Steve, Liau Linda M, Cloughesy Timothy F, Mischel Paul S, Nelson Stanley F Gene expression profiling identifies molecular subtypes of gliomas.. Oncogene. 2003; 22(31): 4918-23.
Shai R, Shi T, Kremen TJ, Horvath S, Liau LM, Cloughesy TF, Mischel PS, Nelson SF Gene expression profiling identifies molecular subtypes of gliomas.. Oncogene. . 2003; 22(31): 4918-23.
Mischel PS, Shai R, Shi T, Horvath S, Lu KV, Choe G, Seligson D, Kremen TJ, Palotie A, Liau LM, Cloughesy TF, Nelson SF Identification of molecular subtypes of glioblastoma by gene expression profiling.. Oncogene. . 2003; 22(15): 2361-73.
Mischel Paul S, Shai Ruty, Shi Tao, Horvath Steve, Lu Kan V, Choe Gheeyoung, Seligson David, Kremen Thomas J, Palotie Aarno, Liau Linda M, Cloughesy Timothy F, Nelson Stanley F Identification of molecular subtypes of glioblastoma by gene expression profiling.. Oncogene. 2003; 22(15): 2361-73.
Mischel PS, Nelson SF, Cloughesy TF Molecular analysis of glioblastoma: pathway profiling and its implications for patient therapy.. Cancer biology & therapy. . 2003; 2(3): 242-7.
Fisher Simon E, Francks Clyde, McCracken James T, McGough James J, Marlow Angela J, MacPhie I Laurence, Newbury Dianne F, Crawford Lori R, Palmer Christina G S, Woodward J Arthur, Del'Homme Melissa, Cantwell Dennis P, Nelson Stanley F, Monaco Anthony P, Smalley Susan L A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.. Am. J. Hum. Genet.. 2002; 70(5): 1183-96.
Smalley Susan L, Kustanovich Vlad, Minassian Sonia L, Stone Jennifer L, Ogdie Matthew N, McGough James J, McCracken James T, MacPhie I Laurence, Francks Clyde, Fisher Simon E, Cantor Rita M, Monaco Anthony P, Nelson Stanley F Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.. Am. J. Hum. Genet.. 2002; 71(4): 959-63.
Nishitani Junko, Chen Zugen, Qin Min, Liu Feng, Chen Hongying, Nelson Stanley F, Liu Xuan Identification of genes required for immortalization in human papillomavirus-infected human oral keratinocytes.. Cell. Mol. Biol. (Noisy-le-grand). 2002; 48 Online Pub(5): OL331-41.
Welford SM, Gregg J, Chen E, Garrison D, Sorensen PH, Denny CT, Nelson SF Detection of differentially expressed genes in primary tumor tissues using representational differences analysis coupled to microarray hybridization.. Nucleic acids research. . 1998; 26(12): 3059-65.
Smalley SL, Bailey JN, Palmer CG, Cantwell DP, McGough JJ, Del'Homme MA, Asarnow JR, Woodward JA, Ramsey C, Nelson SF Evidence that the dopamine D4 receptor is a susceptibility gene in. Molecular Psychiatry 1998; 3(5): 427-30.
Cheung VG, Nelson SF Genomic mismatch scanning identifies human genomic DNA shared identical by descent.. Genomics. . 1998; 47(1): 1-6.
Geschwind DH, Gregg J, Boone K, Karrim J, Pawlikowska-Haddal A, Rao E, Ellison J, Ciccodicola A, D'Urso M, Woods R, et al. Klinefelter's syndrome as a model of anomalous cerebral laterality:. Developmental Genetics 1998; 23(3): 215-29.
Cheung V, Gregg J, Gogolin-Ewens K, Bandong J, Stanley C, Baker L, Higgins M, Nowak N, Shows T, Ewens W, Nelson SF and Speilman R Linkage disequilibrium mapping without genotyping.. Nature Genetics 1998; 18: 225-230.
Baloh RW, Yue Q, Furman JM, Nelson SF Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p.. Annals of neurology. . 1997; 41(1): 8-16.
Geschwind DH, Rhee R, Nelson SF A biotinylated MutS fusion protein and its use in a rapid mutation screening technique.. Genetic analysis : biomolecular engineering. . 1996; 13(4): 105-11.
Cheung VG, Nelson SF Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA.. Proceedings of the National Academy of Sciences of the United States of America. . 1996; 93(25): 14676-9.
Kramer PL, Yue Q, Gancher ST, Nutt JG, Baloh R, Smith E, Browne D, Bussey K, Lovrien E, Nelson S A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p.. American journal of human genetics. . 1995; 57(1): 182-5.
Nelson SF Genomic mismatch scanning: current progress and potential applications.. Electrophoresis. . 1995; 16(2): 279-85.
Nelson SF, Sander M, Kee Y, McCusker J, Modrich P and Brown PO Genomic mismatch scanning: a new approach to genetic linkage mapping.. Nature Genetics 1993; 4: 11-18.


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