Literature DB >> 11073540

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.

M Bugge1, G Bruun-Petersen, K Brøndum-Nielsen, U Friedrich, J Hansen, G Jensen, P K Jensen, U Kristoffersson, C Lundsteen, E Niebuhr, K R Rasmussen, K Rasmussen, N Tommerup.   

Abstract

Disease associated balanced chromosomal rearrangements (DBCRs), which truncate, delete, or otherwise inactivate specific genes, have been instrumental for positional cloning of many disease genes. A network of cytogenetic laboratories, Mendelian Cytogenetics Network (MCN), has been established to facilitate the identification and mapping of DBCRs. To get an estimate of the potential of this approach, we surveyed all cytogenetic archives in Denmark and southern Sweden, with a population of approximately 6.6 million. The nine laboratories have performed 71 739 postnatal cytogenetic tests. Excluding Robertsonian translocations and chromosome 9 inversions, we identified 216 DBCRs ( approximately 0.3%), including a minimum estimate of 114 de novo reciprocal translocations (0.16%) and eight de novo inversions (0.01%). Altogether, this is six times more frequent than in the general population, suggesting a causal relationship with the traits involved in most of these cases. Of the identified cases, only 25 (12%) have been published, including 12 cases with known syndromes and 13 cases with unspecified mental retardation/congenital malformations. The remaining DBCRs were associated with a plethora of traits including mental retardation, dysmorphic features, major congenital malformations, autism, and male and female infertility. Several of the unpublished DBCRs defined candidate breakpoints for nail-patella, Prader-Willi, and Schmidt syndromes, ataxia, and ulna aplasia. The implication of the survey is apparent when compared with MCN; altogether, the 292 participating laboratories have performed >2.5 million postnatal analyses, with an estimated approximately 7500 DBCRs stored in their archives, of which more than half might be causative mutations. In addition, an estimated 450-500 novel cases should be detected each year. Our data illustrate that DBCRs and MCN are resources for large scale establishment of phenotype-genotype relationships in man.

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Year:  2000        PMID: 11073540      PMCID: PMC1734480          DOI: 10.1136/jmg.37.11.858

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  39 in total

1.  Autosomal reciprocal translocations in newborn children and their relatives.

Authors:  U Friedrich; J Nielsen
Journal:  Humangenetik       Date:  1974-02-21

2.  Presumably balanced translocations involving the same band of chromosome No. 4 found in two mentally retarded, dysmorphic individuals.

Authors:  F Skovby; E Niebuhr
Journal:  Ann Genet       Date:  1974-12

3.  Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Authors:  D H Ledbetter; V M Riccardi; S D Airhart; R J Strobel; B S Keenan; J D Crawford
Journal:  N Engl J Med       Date:  1981-02-05       Impact factor: 91.245

4.  Chromosomal studies of children with developmental language retardation.

Authors:  U Friedrich; M Dalby; T Staehelin-Jensen; G Bruun-Petersen
Journal:  Dev Med Child Neurol       Date:  1982-10       Impact factor: 5.449

5.  A, 1;6, translocation associated with congenital glaucoma and cleft lip and palate.

Authors:  S Tinning; P Jacobsen; M Mikkelsen
Journal:  Hum Hered       Date:  1975       Impact factor: 0.444

6.  Fragile site long arm chromosome 16.

Authors:  K Sørensen; J Nielsen; V Holm; J Haahr
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

7.  Follow-up of 32 children with autosomal translocations found among 11,148 consecutively newborn children from 1969 to 1974.

Authors:  J Nielsen; B Krag-Olsen
Journal:  Clin Genet       Date:  1981-07       Impact factor: 4.438

8.  Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34.

Authors:  M A Ferguson-Smith; D A Aitken; C Turleau; J de Grouchy
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

9.  Congenital adrenal hyperplasia associated with a balanced 13--18 translocation.

Authors:  F Petersen; F U Knudsen; M D Nielsen; M Mikkelsen
Journal:  Eur J Pediatr       Date:  1980-05       Impact factor: 3.183

10.  Mental retardation associated with "balanced" chromosome rearrangements.

Authors:  S J Funderburk; M A Spence; R S Sparkes
Journal:  Am J Hum Genet       Date:  1977-03       Impact factor: 11.025

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  22 in total

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2.  Clinical and genomic heterogeneity of Diamond Blackfan anemia in the Russian Federation.

Authors:  Natalia S Smetanina; Irina V Mersiyanova; Maria A Kurnikova; Galina S Ovsyannikova; Lili A Hachatryan; Vlasta O Bobrynina; Michael A Maschan; Galina A Novichkova; Jeffrey M Lipton; Alexey A Maschan
Journal:  Pediatr Blood Cancer       Date:  2015-05-06       Impact factor: 3.167

3.  Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.

Authors:  Stephan J Sanders; A Gulhan Ercan-Sencicek; Vanessa Hus; Rui Luo; Michael T Murtha; Daniel Moreno-De-Luca; Su H Chu; Michael P Moreau; Abha R Gupta; Susanne A Thomson; Christopher E Mason; Kaya Bilguvar; Patricia B S Celestino-Soper; Murim Choi; Emily L Crawford; Lea Davis; Nicole R Davis Wright; Rahul M Dhodapkar; Michael DiCola; Nicholas M DiLullo; Thomas V Fernandez; Vikram Fielding-Singh; Daniel O Fishman; Stephanie Frahm; Rouben Garagaloyan; Gerald S Goh; Sindhuja Kammela; Lambertus Klei; Jennifer K Lowe; Sabata C Lund; Anna D McGrew; Kyle A Meyer; William J Moffat; John D Murdoch; Brian J O'Roak; Gordon T Ober; Rebecca S Pottenger; Melanie J Raubeson; Youeun Song; Qi Wang; Brian L Yaspan; Timothy W Yu; Ilana R Yurkiewicz; Arthur L Beaudet; Rita M Cantor; Martin Curland; Dorothy E Grice; Murat Günel; Richard P Lifton; Shrikant M Mane; Donna M Martin; Chad A Shaw; Michael Sheldon; Jay A Tischfield; Christopher A Walsh; Eric M Morrow; David H Ledbetter; Eric Fombonne; Catherine Lord; Christa Lese Martin; Andrew I Brooks; James S Sutcliffe; Edwin H Cook; Daniel Geschwind; Kathryn Roeder; Bernie Devlin; Matthew W State
Journal:  Neuron       Date:  2011-06-09       Impact factor: 17.173

4.  Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infections.

Authors:  Y Yue; K Stout; B Grossmann; U Zechner; A Brinckmann; C White; D T Pilz; T Haaf
Journal:  J Med Genet       Date:  2005-05-20       Impact factor: 6.318

5.  Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a approximately 0.5-Mb submicroscopic deletion in a patient with mild mental retardation.

Authors:  Katarzyna Borg; Paweł Stankiewicz; Ewa Bocian; Anna Kruczek; Ewa Obersztyn; James R Lupski; Tadeusz Mazurczak
Journal:  Hum Genet       Date:  2005-11-15       Impact factor: 4.132

6.  A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations.

Authors:  Carlos Córdova-Fletes; Ma Guadalupe Domínguez; Ilse Delint-Ramirez; Herminia G Martínez-Rodríguez; Ana María Rivas-Estilla; Patricio Barros-Núñez; Rocío Ortiz-López; Vivian Alejandra Neira
Journal:  Neurogenetics       Date:  2015-07-11       Impact factor: 2.660

7.  SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis.

Authors:  Stavros Bashiardes; Rose Veile; Missy Allen; Carol A Wise; Mathew Dobbs; Jose A Morcuende; Lazlos Szappanos; John A Herring; Anne M Bowcock; Michael Lovett
Journal:  Hum Genet       Date:  2004-04-16       Impact factor: 4.132

8.  Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.

Authors:  B Vona; C Neuner; N El Hajj; E Schneider; R Farcas; V Beyer; U Zechner; A Keilmann; M Poot; O Bartsch; I Nanda; T Haaf
Journal:  Mol Syndromol       Date:  2013-10-04

Review 9.  New perspectives for the elucidation of genetic disorders.

Authors:  Hans-Hilger Ropers
Journal:  Am J Hum Genet       Date:  2007-06-29       Impact factor: 11.025

10.  Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation.

Authors:  Hussein Daoud; Nicolas Gruchy; Jean-Marc Constans; Edgar Moussaoui; Simone Saumureau; Nadia Bayou; Maïté Amy; Sylviane Védrine; Phi Yen Vu; Agnès Rötig; Frédéric Laumonnier; Patrick Vourc'h; Christian R Andres; Nathalie Leporrier; Sylvain Briault
Journal:  Hum Genet       Date:  2008-11-16       Impact factor: 4.132

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