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Editors' Corner

This Month in the Journal p1023

Robin E. Williamson

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This Month in Genetics p1025

Kathryn B. Garber

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2007 ASHG Awards and Addresses

Awards and Addresses Summary p1027

Abstract | | (41 kb)

ASHG Presidential Address: Who Is under the Umbrella—and Why Are We Here? p1029

Wylie Burke

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Allan Award Introduction: Arthur L. Beaudet p1032

James R. Lupski

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Allan Award Lecture: Rare Patients Leading to Epigenetics and Back to Genetics p1034

Arthur L. Beaudet

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Articles

Linkage Disequilibrium between STRPs and SNPs across the Human Genome p1039

Bret A. Payseur, Michael Place, James L. Weber

Abstract | | (372 kb)

Consistently Replicating Locus Linked to Migraine on 10q22-q23 p1051

Verneri Anttila, Dale R. Nyholt, Mikko Kallela, Ville Artto, Salli Vepsäläinen, Eveliina Jakkula, Annika Wennerström, Päivi Tikka-Kleemola, Mari A. Kaunisto, Eija Hämäläinen, Elisabeth Widén, Joseph Terwilliger, Kathleen Merikangas, Grant W. Montgomery, Nicholas G. Martin, Mark Daly, Jaakko Kaprio, Leena Peltonen, Markus Färkkilä, Maija Wessman, Aarno Palotie

Abstract | | (1152 kb) | Supplemental Data

Estimating Odds Ratios in Genome Scans: An Approximate Conditional Likelihood Approach p1064

Arpita Ghosh, Fei Zou, Fred A. Wright

Abstract | | (793 kb) | Supplemental Data

Evidence for Natural Selection on Leukocyte Immunoglobulin-like Receptors for HLA Class I in Northeast Asians p1075

Kouyuki Hirayasu, Jun Ohashi, Hidenori Tanaka, Koichi Kashiwase, Atsuko Ogawa, Minoko Takanashi, Masahiro Satake, Guan Jun Jia, Nyam-Osor Chimge, Elena W. Sideltseva, Katsushi Tokunaga, Toshio Yabe

Abstract | | (901 kb)

Mitochondrial Genome Diversity in Arctic Siberians, with Particular Reference to the Evolutionary History of Beringia and Pleistocenic Peopling of the Americas p1084

Natalia V. Volodko, Elena B. Starikovskaya, Ilya O. Mazunin, Nikolai P. Eltsov, Polina V. Naidenko, Douglas C. Wallace, Rem I. Sukernik

Abstract | | (526 kb)

Genetic Architecture of Transcript-Level Variation in Humans p1101

Shiwei Duan, R. Stephanie Huang, Wei Zhang, Wasim K. Bleibel, Cheryl A. Roe, Tyson A. Clark, Tina X. Chen, Anthony C. Schweitzer, John E. Blume, Nancy J. Cox, M. Eileen Dolan

Abstract | | (2471 kb) | Supplemental Data

Alopecia, Neurological Defects, and Endocrinopathy Syndrome Caused by Decreased Expression of RBM28, a Nucleolar Protein Associated with Ribosome Biogenesis p1114

Janna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, Margarita Indelman, Ayelet Shani-Adir, Noam Adir, Ehud Lipkin, Sivan Bercovici, Dan Geiger, Maurice A. van Steensel, Peter M. Steijlen, Reuven Bergman, Albrecht Bindereif, Mordechai Choder, Stavit Shalev, Eli Sprecher

Abstract | | (1086 kb) | Supplemental Data

A Functional Polymorphism in THBS2 that Affects Alternative Splicing and MMP Binding Is Associated with Lumbar-Disc Herniation p1122

Yuichiro Hirose, Kazuhiro Chiba, Tatsuki Karasugi, Masahiro Nakajima, Yoshiharu Kawaguchi, Yasuo Mikami, Tatsuya Furuichi, Futoshi Mio, Atsushi Miyake, Takeshi Miyamoto, Kouichi Ozaki, Atsushi Takahashi, Hiroshi Mizuta, Toshikazu Kubo, Tomoatsu Kimura, Toshihiro Tanaka, Yoshiaki Toyama, Shiro Ikegawa

Abstract | | (393 kb)

Sponsored Article
The Dawn of Human Matrilineal Diversity p1130

Doron M. Behar, Richard Villems, Himla Soodyall, Jason Blue-Smith, Luisa Pereira, Ene Metspalu, Rosaria Scozzari, Heeran Makkan, Shay Tzur, David Comas, Jaume Bertranpetit, Lluis Quintana-Murci, Chris Tyler-Smith, R. Spencer Wells, Saharon Rosset

Abstract | | (770 kb) | Supplemental Data

Differential Expression of PTEN-Targeting MicroRNAs miR-19a and miR-21 in Cowden Syndrome p1141

Marcus G. Pezzolesi, Petra Platzer, Kristin A. Waite, Charis Eng

Abstract | | (375 kb) | Supplemental Data

Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation p1150

Florence Molinari, François Foulquier, Patrick S. Tarpey, Willy Morelle, Sarah Boissel, Jon Teague, Sarah Edkins, P. Andrew Futreal, Michael R. Stratton, Gillian Turner, Gert Matthijs, Jozef Gecz, Arnold Munnich, Laurence Colleaux

Abstract | | (1206 kb)

Reports

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation p1158

Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana Kariminejad, Farkhondeh Behjati, Andreas Tzschach, Hossein Najmabadi, Hans Hilger Ropers, Andreas Walter Kuss

Abstract | | (1196 kb)

Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly p1165

Rikke S. Møller, Sabine Kübart, Maria Hoeltzenbein, Babett Heye, Ida Vogel, Christian P. Hansen, Corinna Menzel, Reinhard Ullmann, Niels Tommerup, Hans-Hilger Ropers, Zeynep Tümer, Vera M. Kalscheuer

Abstract | | (703 kb)

TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome p1171

Jeff M. Milunsky, Tom A. Maher, Geping Zhao, Amy E. Roberts, Heather J. Stalker, Roberto T. Zori, Michelle N. Burch, Michele Clemens, John B. Mulliken, Rosemarie Smith, Angela E. Lin

Abstract | | (692 kb)

Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome p1178

Daniel F. Schorderet, Olivia Nichini, Gaëlle Boisset, Bozena Polok, Leila Tiab, Hélène Mayeur, Bahija Raji, Gauillaume de la Houssaye, Marc M. Abitbol, Francis L. Munier

Abstract | | (2282 kb) | Supplemental Data

Loci Related to Metabolic-Syndrome Pathways Including LEPR,HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study p1185

Paul M. Ridker, Guillaume Pare, Alex Parker, Robert Y.L. Zee, Jacqueline S. Danik, Julie E. Buring, David Kwiatkowski, Nancy R. Cook, Joseph P. Miletich, Daniel I. Chasman

Abstract | | (844 kb)

Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1α are Associated with C-Reactive Protein p1193

Alexander P. Reiner, Mathew J. Barber, Yongtao Guan, Paul M. Ridker, Leslie A. Lange, Daniel I. Chasman, Jeremy D. Walston, Gregory M. Cooper, Nancy S. Jenny, Mark J. Rieder, J. Peter Durda, Joshua D. Smith, John Novembre, Russell P. Tracy, Jerome I. Rotter, Matthew Stephens, Deborah A. Nickerson, Ronald M. Krauss

Abstract | | (401 kb)

Genetic Analysis of Innate Immunity in Crohn's Disease and Ulcerative Colitis Identifies Two Susceptibility Loci Harboring CARD9 and IL18RAP p1202

Alexandra Zhernakova, Eleanora M. Festen, Lude Franke, Gosia Trynka, Cleo C. van Diemen, Alienke J. Monsuur, Marianna Bevova, Rian M. Nijmeijer, Ruben van ‘t Slot, Roel Heijmans, H. Marike Boezen, David A. van Heel, Adriaan A. van Bodegraven, Pieter C.F. Stokkers, Cisca Wijmenga, J. Bart A. Crusius, Rinse K. Weersma

Abstract | | (184 kb) | Supplemental Data

Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ p1211

Ortal Barel, Zamir Shorer, Hagit Flusser, Rivka Ofir, Ginat Narkis, Gal Finer, Hanah Shalev, Ahmad Nasasra, Ann Saada, Ohad S. Birk

Abstract | | (856 kb) | Supplemental Data

Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome p1217

Almogit Abu, Moshe Frydman, Dina Marek, Eran Pras, Uri Nir, Haike Reznik-Wolf, Elon Pras

Abstract | | (717 kb) | Supplemental Data

Erratum

Evaluation of Genetic Variation Contributing to Differences in Gene Expression between Populations p1223

Wei Zhang, Shiwei Duan, Emily O. Kistner, Wasim K. Bleibel, R. Stephanie Huang, Tyson A. Clark, Tina X. Chen, Anthony C. Schweitzer, John E. Blume, Nancy J. Cox, M. Eileen Dolan

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Correction

Estimating Odds Ratios in Genome Scans: An Approximate Conditional Likelihood Approach p1224

Arpita Ghosh, Fei Zou, Fred A. Wright

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Announcements

Employment Opportunities and Fellowship p1225

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