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Birgit Funke

Research Profile

Anatomy

Disorders

Living Beings

Physiology

Chemicals & Drugs

Procedures

Genes & Molecular Sequences

Single Nucleotide Polymorphism

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Publications

TOP 3
Neal K Lakdawala; Nancy J Mendelsohn; Chantal Morel; Apostolos Psychogios; Heidi L Rehm; Amy E Roberts; Christine E Seidman; Jonathan G Seidman; Emily White; Samantha Baxter; Melanie Care; Wendy K Chung; Allison L Cirino; Elizabeth Duffy; Birgit Funke; Nicole Johnson; Carolyn Jones; Daniel P Judge; Carolyn Y Ho
Genetic testing for dilated cardiomyopathy in clinical practice.
Polakit Teekakirikul; Stephanie Cox; Birgit Funke; Heidi L Rehm
Targeted sequencing using Affymetrix CustomSeq Arrays.
Go Suzuki; Kathryn M Harper; Takeshi Hiramoto; Birgit Funke; MoonSook Lee; Gina Kang; Mahalah Buell; Mark A Geyer; Raju Kucherlapati; Bernice E Morrow; Pekka T Männistö; Soh Agatsuma; Noboru Hiroi
Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice.

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All Publications

2012: Neal K Lakdawala; Nancy J Mendelsohn; Chantal Morel; Apostolos Psychogios; Heidi L Rehm; Amy E Roberts; Christine E Seidman; Jonathan G Seidman; Emily White; Samantha Baxter; Melanie Care; Wendy K Chung; Allison L Cirino; Elizabeth Duffy; Birgit Funke; Nicole Johnson; Carolyn Jones; Daniel P Judge; Carolyn Y Ho
Genetic testing for dilated cardiomyopathy in clinical practice.
Journal of cardiac failure 2012;18(4):296-303.
2011: Polakit Teekakirikul; Stephanie Cox; Birgit Funke; Heidi L Rehm
Targeted sequencing using Affymetrix CustomSeq Arrays.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2011;Chapter 7():Unit7.18.
2009: Go Suzuki; Kathryn M Harper; Takeshi Hiramoto; Birgit Funke; MoonSook Lee; Gina Kang; Mahalah Buell; Mark A Geyer; Raju Kucherlapati; Bernice E Morrow; Pekka T Männistö; Soh Agatsuma; Noboru Hiroi
Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice.
Human molecular genetics 2009;18(20):3914-25.
2007: Birgit Funke; Todd Lencz; Christine T Finn; Pamela DeRosse; G David Poznik; Alex M Plocik; John M Kane; John J Rogus; Anil Malhotra; Raju Kucherlapati
Analysis of TBX1 variation in patients with psychotic and affective disorders.
Molecular medicine (Cambridge, Mass.) 2007;13(7-8):407-14.
2007: Katherine Burdick; Birgit Funke; Joseph F Goldberg; John A Bates; Judith Jaeger; Raju Kucherlapati; Anil Malhotra
COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance.
Bipolar disorders 2007;9(4):370-6.
2007: Birgit Funke; Alison C Brown; Marco F Ramoni; Maura E Regan; Chris Baglieri; Christine T Finn; Melanie Babcock; Robert J Shprintzen; Bernice E Morrow; Raju Kucherlapati
A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions.
Genetic testing 2007;11(1):91-100.
2007: Katherine Burdick; Terry Goldberg; Birgit Funke; John A Bates; Todd Lencz; Raju Kucherlapati; Anil Malhotra
DTNBP1 genotype influences cognitive decline in schizophrenia.
Schizophrenia research 2007;89(1-3):169-72.
2006: Jeffrey M Long; Patricia LaPorte; Sandra Merscher-gomez; Birgit Funke; Bruno Saint-Jore; Anne Puech; Raju Kucherlapati; Bernice E Morrow; Arthur I Skoultchi; Anthony Wynshaw-Boris
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome.
Neurogenetics 2006;7(4):247-57.
2006: Pamela DeRosse; Birgit Funke; Katherine Burdick; Todd Lencz; Terry Goldberg; John M Kane; Raju Kucherlapati; Anil Malhotra
COMT genotype and manic symptoms in schizophrenia.
Schizophrenia research 2006;87(1-3):28-31.
2006: Katherine Burdick; Todd Lencz; Birgit Funke; Christine T Finn; Philip Szeszko; John M Kane; Raju Kucherlapati; Anil Malhotra
Genetic variation in DTNBP1 influences general cognitive ability.
Human molecular genetics 2006;15(10):1563-8.
2006: Wendy R Kates; Kevin M Antshel; Nuria AbdulSabur; Deirdre Colgan; Birgit Funke; Wanda Fremont; Anne Marie Higgins; Raju Kucherlapati; Robert J Shprintzen
A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(3):274-80.
2006: Pamela DeRosse; Birgit Funke; Katherine Burdick; Todd Lencz; Jenny M Ekholm; John M Kane; Raju Kucherlapati; Anil Malhotra
Dysbindin genotype and negative symptoms in schizophrenia.
The American journal of psychiatry 2006;163(3):532-4.
2005: Noboru Hiroi; Hongwen Zhu; MoonSook Lee; Birgit Funke; Makoto Arai; Masanari Itokawa; Raju Kucherlapati; Bernice E Morrow; Takehito Sawamura; Soh Agatsuma
A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(52):19132-7.
2005: Birgit Funke; Anil Malhotra; Christine T Finn; Alex M Plocik; Stephen L Lake; Todd Lencz; Pamela DeRosse; John M Kane; Raju Kucherlapati
COMT genetic variation confers risk for psychotic and affective disorders: a case control study.
Behavioral and brain functions : BBF 2005;1():19.
2004: Birgit Funke; Christine T Finn; Alex M Plocik; Stephen L Lake; Pamela DeRosse; John M Kane; Raju Kucherlapati; Anil Malhotra
Association of the DTNBP1 locus with schizophrenia in a U.S. population.
American journal of human genetics 2004;75(5):891-8.
2002: Susan J Gross; Jose Carlos Ferreira; Bernice E Morrow; Pe'er Dar; Birgit Funke; Dineo Khabele; Irwin R Merkatz
Gene expression profile of trisomy 21 placentas: a potential approach for designing noninvasive techniques of prenatal diagnosis.
American journal of obstetrics and gynecology 2002;187(2):457-62.
2001: Birgit Funke; Jonathan A Epstein; Lazaros Kochilas; M M Lu; RK Pandita; Jun Liao; R Bauerndistel; T Schüler; Hubert Schorle; M Christian Brown; J Adams; Bernice E Morrow
Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.
Human molecular genetics 2001;10(22):2549-56.
2001: Birgit Funke; RK Pandita; Bernice E Morrow
Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.
Genomics 2001;73(3):264-71.
2001: Sandra Merscher-gomez; Birgit Funke; Jonathan A Epstein; Joerg Heyer; Anne Puech; M M Lu; R J Xavier; M B Demay; R G Russell; Stephen M Factor; K Tokooya; B S Jore; M Lopez; RK Pandita; Mariel Lia; D Carrion; H Xu; Hubert Schorle; J B Kobler; Peter J Scambler; Anthony Wynshaw-Boris; Arthur I Skoultchi; Bernice E Morrow; Raju Kucherlapati
TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
Cell 2001;104(4):619-29.
2000: J Maldonado-Saldivia; Birgit Funke; RK Pandita; T Schüler; Bernice E Morrow; Hubert Schorle
Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome.
Mechanisms of development 2000;96(1):121-4.
1999: L Edelmann; RK Pandita; Elizabeth Spiteri; Birgit Funke; R Goldberg; Nallasivam Palanisamy; Raju S K Chaganti; E Magenis; Robert J Shprintzen; Bernice E Morrow
A common molecular basis for rearrangement disorders on chromosome 22q11.
Human molecular genetics 1999;8(7):1157-67.
1999: Birgit Funke; L Edelmann; N McCain; RK Pandita; Jose Carlos Ferreira; Sandra Merscher-gomez; M Zohouri; Linda Cannizzaro; Alan L Shanske; Bernice E Morrow
Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.
American journal of human genetics 1999;64(3):747-58.
1998: Birgit Funke; Anne Puech; Bruno Saint-Jore; RK Pandita; Arthur I Skoultchi; Bernice E Morrow
Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.
Genomics 1998;53(2):146-54.
1997: Anne Puech; Bruno Saint-Jore; Birgit Funke; D J Gilbert; H Sirotkin; N G Copeland; N A Jenkins; Raju Kucherlapati; Bernice E Morrow; Arthur I Skoultchi
Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(26):14608-13.
1997: Birgit Funke; Bruno Saint-Jore; Anne Puech; H Sirotkin; L Edelmann; C Carlson; S Raft; RK Pandita; Raju Kucherlapati; Arthur I Skoultchi; Bernice E Morrow
Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11.
Genomics 1997;46(3):364-72.