string(238) "select * FROM articoli_opac WHERE fonte <> 'ISI' AND fonte='ACNP' AND fasc_anno_pubbl='2004' AND fasc_issn='00029297' order by level desc, fasc_key desc, NULLIF(regexp_replace(pagina_ini, E'\\D', '', 'g'), '')::int asc offset 75 limit 25" ACNP - Italian Periodicals Catalogue

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Articles table of contents

Results : 76-100/138

Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations

Authors: Crawford, Dana C. Carlson, Christopher S. Rieder, Mark J. Carrington, Dana P. Yi, Qiuan Smith, Joshua D. Eberle, Michael A. Kruglyak, Leonid Nickerson, Deborah A.

Journal: American journal of human genetics

Citation: C. Crawford, Dana et al., Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations, American journal of human genetics , 74(4), 2004, pp. 610-622

Crohn Disease: Frequency and Nature of CARD15 Mutations in Ashkenazi and Sephardi/Oriental Jewish Families

Authors: Tukel, Turgut Present, Daniel Rachmilewitz, Daniel Mayer, Lloyd Grant, Deniera Risch, Neil Shalata, Adel Desnick, Robert J.

Journal: American journal of human genetics

Citation: Tukel, Turgut et al., Crohn Disease: Frequency and Nature of CARD15 Mutations in Ashkenazi and Sephardi/Oriental Jewish Families, American journal of human genetics , 74(4), 2004, pp. 623-636

Polymorphisms in the Trace Amine Receptor 4 (TRAR4) Gene on Chromosome 6q23.2 Are Associated with Susceptibility to Schizophrenia

Authors: Duan, Jubao Martinez, Maria Sanders, Alan R. Hou, Cuiping Saitou, Naruya Kitano, Takashi Mowry, Bryan J. Crowe, Raymond R. Silverman, Jeremy M. Levinson, Douglas F. Gejman, Pablo V.

Journal: American journal of human genetics

Citation: Duan, Jubao et al., Polymorphisms in the Trace Amine Receptor 4 (TRAR4) Gene on Chromosome 6q23.2 Are Associated with Susceptibility to Schizophrenia, American journal of human genetics , 75(4), 2004, pp. 624-638

Natural Selection and Molecular Evolution in PTC, a Bitter-Taste Receptor Gene

Authors: Wooding, Stephen Kim, Un-kyung Bamshad, M.J. Larsen, Jennifer Jorde, Lynn B. Drayna, Dennis

Journal: American journal of human genetics

Citation: Wooding, Stephen et al., Natural Selection and Molecular Evolution in PTC, a Bitter-Taste Receptor Gene, American journal of human genetics , 74(4), 2004, pp. 637-646

Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis

Authors: Perrault, Isabelle Hanein, Sylvain Gerber, Sylvie Barbet, Fabienne Ducroq, Dominique Dollfus, Helene Hamel, Christian Dufier, Jean-Louis Munnich, Arnold Kaplan, Josseline Rozet, Jean-Michal

Journal: American journal of human genetics

Citation: Perrault, Isabelle et al., Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis, American journal of human genetics , 75(4), 2004, pp. 639-646

Sequence-Based Linkage Analysis

Authors: Furman, Itay Rieder, Mark J. de Ponte, Suzanne Carrington, Dana P. Nickerson, Deborah A. Kruglyak, Leonid Markianos, Kyriacos

Journal: American journal of human genetics

Citation: Furman, Itay et al., Sequence-Based Linkage Analysis, American journal of human genetics , 75(4), 2004, pp. 647-653

Novel Analytical Methods Applied to Type 1 Diabetes Genome-Scan Data

Authors: Pociot, Flemming Karlsen, Allan E. Pendersen, Claus B. Aalund, Mogens Nerup, Jørn European Consortium for IDDM Genome Studies

Journal: American journal of human genetics

Citation: Pociot, Flemming et al., Novel Analytical Methods Applied to Type 1 Diabetes Genome-Scan Data, American journal of human genetics , 74(4), 2004, pp. 647-660

The Western and Eastern Roots of the Saami.the Story of Genetic .Outliers. Told by Mitochondrial DNA and Y Chromosomes

Authors: Tambets, Kristiina Rootsi, Siiri Kivisild, Toomas Help, Hela Serk, Piia Loogväli, Eva-Liis Tolk, Helle-Viivi Reidla, Maere Metspalu, Ene Pliss, Liana Balanovsky, Oleg Pshenichnov, Andrey Balanovska, Elena Gubina, Marina Zhadanov, Sergey Osipova, Ludmila Damba, Larisa Voevoda, Mikhail Kutuev, Ildus Bermisheva, Marina Khusnutdinova, Elza Gusar, Vladislava Grechanina, Elena Parik, Jüri Pennarun, Erwan Richard, Christelle Chaventre, Andre Moisan, Jean-Paul Bara., Lovorka Peri.i., Marijana Rudan, Pavao Terzi., Rifat Mikerezi, Ilia Krumina, Astrida Baumanis, Viesturs Koziel, Slawomir Rickards, Olga De Stefano, Gian Franco Anagnou, Nicholas Pappa, Kalliopi I. Michalodimitrakis, Emmanuel Feràk, Vladimir Füredi, Sandor Komel, Radovan Beckman, Lars Villems. Richard

Journal: American journal of human genetics

Citation: Tambets, Kristiina et al., The Western and Eastern Roots of the Saami.the Story of Genetic .Outliers. Told by Mitochondrial DNA and Y Chromosomes, American journal of human genetics , 74(4), 2004, pp. 661-682

Power for Genetic Association Studies with Random Allele Frequencies and Genotype Distributions

Authors: Ambrosius, Walter T. Lange, Ethan M. Langefeld, Carl D.

Journal: American journal of human genetics

Citation: T. Ambrosius, Walter et al., Power for Genetic Association Studies with Random Allele Frequencies and Genotype Distributions, American journal of human genetics , 74(4), 2004, pp. 683-693

The Etruscans: A Population-Genetic Study

Authors: Vernesi, Cristiano Caramelli, David Dupanloup, Isabelle Bertorelle, Giorgio Lari, Martina Cappellini, Enrico Moggi-Cecchi, Jacopo Chiarelli, Brunetto Castrì, Loredana Casoli, Antonella Mallegni, Francesco Lalueza-Fox, Carles Barbujani, Guido

Journal: American journal of human genetics

Citation: Vernesi, Cristiano et al., The Etruscans: A Population-Genetic Study, American journal of human genetics , 74(4), 2004, pp. 694-704

Variations in GABRA2, Encoding the .2 Subunit of the GABAA Receptor, Are Associated with Alcohol Dependence and with Brain Oscillations

Authors: Edenberg, Howard J. Dick, Danielle M. Xuei, Xiaoling Tian, Huijun Almasy, Laura Bauer, Lance O. Crowe, Raymond R. Goate, Alison Hesselbrock, Victor Jones, Kevin Kwon, Jennifer Li, Ting-Kai Nurnberger, John I., Jr. O'Connor, Sean J. Reich, Theodore Rice, John Schuckit, Marc A. Porjesz, Bernice Foroud, Tatiana Begleiter, Henri

Journal: American journal of human genetics

Citation: J. Edenberg, Howard et al., Variations in GABRA2, Encoding the .2 Subunit of the GABAA Receptor, Are Associated with Alcohol Dependence and with Brain Oscillations, American journal of human genetics , 74(4), 2004, pp. 705-714

Ethiopian Mitochondrial DNA Heritage: Tracking Gene Flow Across and Around the Gate of Tears

Authors: Kivisild, Toomas Reidla, Maere Metspalu, Ene Rosa, Alexandra Brehm, Antonio Pennarun, Erwan Parik, Jüri Geberhiwot, Tarekegn Usanga, Esien Villems, Richard

Journal: American journal of human genetics

Citation: Kivisild, Toomas et al., Ethiopian Mitochondrial DNA Heritage: Tracking Gene Flow Across and Around the Gate of Tears, American journal of human genetics , 75(5), 2004, pp. 752-770

tatistical Tests for Admixture Mapping with Case-Control and Cases-Only Data

Authors: Montana, Giovanni Pritchard, Jonathan K.

Journal: American journal of human genetics

Citation: Montana, Giovanni et K. Pritchard, Jonathan, tatistical Tests for Admixture Mapping with Case-Control and Cases-Only Data, American journal of human genetics , 75(5), 2004, pp. 771-789

Isolated 3-Methylcrotonyl-CoA Carboxylase Deficiency: Evidence for an Allele-Specific Dominant Negative Effect and Responsiveness to Biotin Therapy

Authors: Baumgartner, Matthias R. Dantas, M. Fernanda Suormala, Terttu Almashanu, Shlomo Giunta, Cecilia Friebel, Dolores Gebhardt, Boris Fowler, Brian Hoffmann, Georg F. Baumgartner, E. Regula Valle, David

Journal: American journal of human genetics

Citation: R. Baumgartner, Matthias et al., Isolated 3-Methylcrotonyl-CoA Carboxylase Deficiency: Evidence for an Allele-Specific Dominant Negative Effect and Responsiveness to Biotin Therapy, American journal of human genetics , 75(5), 2004, pp. 790-800

ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome

Authors: Dagoneau, Nathalie Benoist-Lasselin, Catherine Huber, Céline Faivre, Laurence Mégarbané, André Alswaid, Abdulrahman Dollfus, Hélène Alembik, Yves Munnich, Arnold Legeai-Mallet, Laurence Cormier-Daire, Valérie

Journal: American journal of human genetics

Citation: Dagoneau, Nathalie et al., ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome, American journal of human genetics , 75(5), 2004, pp. 801-806

Functional Analysis of Genetic Variation in Catechol-O-Methyltransferase (COMT): Effects on mRNA, Protein, and Enzyme Activity in Postmortem Human Brain

Authors: Chen, Jingshan Lipska, Barbara K. Halim, Nader Ma, Quang D. Matsumoto, Mitsuyuki Melhem, Samer Kolachana, Bhaskar S. Hyde, Thomas M. Herman, Mary M. Apud, Jose Egan, Michael F. Kleinman, Joel E. Weinberger, Daniel R.

Journal: American journal of human genetics

Citation: Chen, Jingshan et al., Functional Analysis of Genetic Variation in Catechol-O-Methyltransferase (COMT): Effects on mRNA, Protein, and Enzyme Activity in Postmortem Human Brain, American journal of human genetics , 75(5), 2004, pp. 807-821

Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2

Authors: Li, Anren Jiao, Xiaodong Munier, Francis L. Schorderet, Daniel F. Yao, Wenliang Iwata, Fumino Hayakawa, Mutsuko Kanai, Atsushi Chen, Muh Shy Lewis, Richard Alan Heckenlively, John Weleber, Richard G. Traboulsi, Elias I. Zhang, Qingjiong Xiao, Xueshan Kaiser-Kupfer, Muriel Sergeev, Yuri V. Fielding Hejtmancik, J.

Journal: American journal of human genetics

Citation: Li, Anren et al., Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2, American journal of human genetics , 74(5), 2004, pp. 817-826

A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis

Authors: Nishimura, Agnes L. Mitne-Neto, Miguel Silva, Helga C.A. Richieri-Costa, Antônio Middleton, Susan Cascio, Duilio Kok, Fernando Oliveira, João R.M. Gillingwater, Tom Webb, Jeanette Skehel, Paul Zatz, Mayana

Journal: American journal of human genetics

Citation: L. Nishimura, Agnes et al., A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis, American journal of human genetics , 75(5), 2004, pp. 822-831

Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor

Authors: Quintana-Murci, Lluìs Chaix, Raphaëlle Spencer Wells, R. Behar, Doron M. Sayar, Hamid Scozzari, Rosaria Rengo, Chiara Al-Zahery, Nadia Semino, Ornella Santachiara-Benerecetti, A. Silvana Coppa, Alfredo Ayub, Qasim Mohyuddin, Aisha Tyler-Smith, Chris Mehdi, S. Qasim Torroni, Antonio McElreavey, Ken

Journal: American journal of human genetics

Citation: Quintana-murci, Lluìs et al., Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor, American journal of human genetics , 74(5), 2004, pp. 827-845

Association of the Gene Encoding Wingless-Type Mammary Tumor Virus Integration-Site Family Member 5B (WNT5B) with Type 2 Diabetes

Authors: Kanazawa, Akio Tsukada, Syuuichi Sekine, Akihiro Tsunoda, Tatsuhiko Takahashi, Atsushi Kashiwagi, Atsunori Tanaka, Yasushi Babazono, Tetsuya Matsuda, Masafumi Kaku, Kohei Iwamoto, Yasuhiko Kawamori, Ryuzo Kikkawa, Ryuichi Nakamura, Yusuke Maeda, Shiro

Journal: American journal of human genetics

Citation: Kanazawa, Akio et al., Association of the Gene Encoding Wingless-Type Mammary Tumor Virus Integration-Site Family Member 5B (WNT5B) with Type 2 Diabetes, American journal of human genetics , 75(5), 2004, pp. 832-843

Microdeletion of LIT1 in Familial Beckwith-Wiedemann Syndrome

Authors: Niemitz, Emily L. DeBaun, Michael R. Fallon, Jonathan Murakami, Kazuhiro Kugoh, Hiroyuki Oshimura, Mitsuo Feinberg, Andrew P.

Journal: American journal of human genetics

Citation: L. Niemitz, Emily et al., Microdeletion of LIT1 in Familial Beckwith-Wiedemann Syndrome, American journal of human genetics , 75(5), 2004, pp. 844-849

Positional Cloning by Linkage Disequilibrium

Authors: Maniatis, Nikolas Collins, Andrew Gibson, Jane Zhang, Weihua Tapper, William Morton, Newton E.

Journal: American journal of human genetics

Citation: Maniatis, Nikolas et al., Positional Cloning by Linkage Disequilibrium, American journal of human genetics , 74(5), 2004, pp. 846-855

Finding Haplotype Tagging SNPs by Use of Principal Components Analysis

Authors: Lin, Zhen Altman, Russ B.

Journal: American journal of human genetics

Citation: Lin, Zhen et B. Altman, Russ, Finding Haplotype Tagging SNPs by Use of Principal Components Analysis, American journal of human genetics , 75(5), 2004, pp. 850-861

Analyses of Genetic Structure of Tibeto-Burman Populations Reveals Sex-Biased Admixture in Southern Tibeto-Burmans

Authors: Wen, Bo Xie, Xuanhua Gao, Song Li, Hui Shi, Hong Song, Xiufeng Qian, Tingzhi Xiao, Chunjie Jin, Jianzhong Su, Bing Lu, Daru Chakraborty, Ranajit Jin, Li

Journal: American journal of human genetics

Citation: Wen, Bo et al., Analyses of Genetic Structure of Tibeto-Burman Populations Reveals Sex-Biased Admixture in Southern Tibeto-Burmans, American journal of human genetics , 74(5), 2004, pp. 856-865

Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder

Authors: Hodgkinson, Colin A. Goldman, David Jaeger, Judith Persaud, Shalini Kane, John M. Lipsky, Robert H. Malhotra, Anil K.

Journal: American journal of human genetics

Citation: A. Hodgkinson, Colin et al., Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder, American journal of human genetics , 75(5), 2004, pp. 862-872

Results: 1-25 | 26-50 | 51-75 | 76-100 | >>