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1

Integrative biology and the developing limb bud

Jeffrey W. Innis, Elliott H. Margulies, Sharon Kardia

Journal:

Evolution & Development

Year:

2002

Language:

english

File:

PDF, 778 KB

english, 2002

2

Mutation of HOXA13 in hand-foot-genital syndrome

Mortlock, Douglas P., Innis, Jeffrey W.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 352 KB

1997

3

Extended Spectrum of Human Glucose-6-Phosphatase Catalytic Subunit 3 Deficiency: Novel Genotypes and Phenotypic Variability in Severe Congenital Neutropenia

Kaan Boztug, Philip S. Rosenberg, Marie Dorda, Siddharth Banka, Thomas Moulton, Julie Curtin, Nima Rezaei, John Corns, Jeffrey W. Innis, Zekai Avci, Hung Chi Tran, Isabelle Pellier, Paolo Pierani, Rac

Journal:

The Journal of Pediatrics

Year:

2012

Language:

english

File:

PDF, 318 KB

english, 2012

4

Familial Large Vestibular Aqueduct Syndrome

Andrew J. Griffith, H. Alexander Arts, Catherine Downs, Jeffrey W. Innis, Neil T. Shepard, Susan Sheldon, Stephen S. Gebarski

Journal:

The Laryngoscope

Year:

1996

Language:

english

File:

PDF, 720 KB

english, 1996

5

Familial Syndromic Esophageal Atresia Maps to 2p23-p24

Jacopo Celli, Ellen van Beusekom, Raoul C.M. Hennekam, M. Esther Gallardo, Dominique F.C.M. Smeets, Santiago Rodríguez de Córdoba, Jeffrey W. Innis, Moshe Frydman, Rainer König, Helen Kingston, John T

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 1.03 MB

english, 2000

6

Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes

Riley, Kacie N., Catalano, Lisa M., Bernat, John A., Adams, Stacie D., Martin, Donna M., Lalani, Seema R., Patel, Ankita, Burnside, Rachel D., Innis, Jeffrey W., Rudd, M. Katharine

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 978 KB

english, 2015

7

Venous blood gas and biochemical analysis of wild captured green turtles (Chelonia mydas) and Kempâs ridley turtles (Lepidochelys kempii) from the Gulf of Mexico

McNally, Kerry L., Mott, Cody R., Guertin, Jeffrey R., Gorham, Jonathan C., Innis, Charles J., Munderloh, Ulrike Gertrud

Journal:

Year:

2020

File:

PDF, 655 KB

2020

8

Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies

Innis, Jeffrey W., Asher, James H., Poznanski, Andrew K., Sheldon, Susan

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 1.79 MB

english, 1997

9

Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia

Innis, Jeffrey W., Asher,, James H., Liang, Yong, Wang, Aihui, Wilke, Charles M., Dierick, Herman A., Kazen-Gillespie, Kristin, Sheldon, Susan, Glover, Thomas W., Friedman, Thomas B.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 380 KB

english, 1997

10

Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth

Innis, Jeffrey W., Sieving, Paul A., McMillan, Pamella, Weatherly, Robert A.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 274 KB

english, 1998

11

Possible third case of Lin-Gettig syndrome

Peter Hedera, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 101 KB

english, 2002

12

Juberg–Hayward syndrome: Report of a new patient with severe phenotype and novel clinical features

Peter Hedera, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 106 KB

english, 2003

13

Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal

Catherine E. Keegan, Eric Vilain, Mansoor Mohammed, Jessica Lehoczky, William B. Dobyns, Steven M. Archer, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 146 KB

english, 2004

14

Two patients with monomelic ulnar duplication with mirror hand polydactyly: Segmental Laurin–Sandrow syndrome

Jeffrey W. Innis, Peter Hedera

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 146 KB

english, 2004

15

Chromosome rearrangements in Cornelia de Lange syndrome (CdLS): Report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements

Cheryl DeScipio, Maninder Kaur, Dinah Yaeger, Jeffrey W. Innis, Nancy B. Spinner, Laird G. Jackson, Ian D. Krantz

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 200 KB

english, 2005

16

Craniofacial dyssynostosis in two boys with apparently normal cognitive development

Sam F. Lahidji, Steven R. Buchman, Karin Muraszko, Jeffrey W. Innis, Catherine E. Keegan

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 181 KB

english, 2006

17

Molecular characterization of HOXA13 polyalanine expansion proteins in hand–foot–genital syndrome

Boris Utsch, Colleen D. McCabe, Kenneth Galbraith, Ricardo Gonzalez, Mark Born, Jörg Dötsch, Michael Ludwig, Heiko Reutter, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 270 KB

english, 2007

18

A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia

Jirair K. Bedoyan, Marci M. Lesperance, Todd Ackley, Ramaswamy K. Iyer, Jeffrey W. Innis, Vinod K. Misra

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 431 KB

english, 2011

19

Multiple congenital anomalies and developmental delay in a boy associated with a de novo 16p13.3 deletion

Marc Nelson, Shane Quinonez, Todd Ackley, Ram K. Iyer, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 477 KB

english, 2011

20

Chromosome 4q deletion syndrome: Narrowing the cardiovascular critical region to 4q32.2–q34.3

Wenbo Xu, Ayesha Ahmad, Susan Dagenais, Ramaswamy K. Iyer, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 152 KB

english, 2012

21

A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome

Jeffrey W. Innis, Frances R. Goodman, Chiara Bacchelli, Thomas M. Williams, Douglas P. Mortlock, Praveen Sateesh, Peter J. Scambler, Wendy McKinnon, Alan E. Guttmacher

Journal:

Year:

2002

Language:

english

File:

PDF, 166 KB

english, 2002

22

Epidemic of adenovirus-induced respiratory illness among US military recruits: Epidemiologic and immunologic risk factors in healthy, young adults

Jose L. Sanchez, Leonard N. Binn, Bruce L. Innis, Richard D. Reynolds, Terrence Lee, Felicia Mitchell-Raymundo, Stephen C. Craig, Jeffrey P. Marquez, Greg A. Shepherd, Christina S. Polyak, Johnnie Con

Journal:

Journal of Medical Virology

Year:

2001

Language:

english

File:

PDF, 155 KB

english, 2001

23

Priming the search for HOX mutations

Jeffrey W. Innis

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2002

Language:

english

File:

PDF, 43 KB

english, 2002

24

Two highly polymorphic CA repeats in the Menkes gene (ATP7A)

Catherine R. Begy, Herman A. Dierick, Jeffrey W. Innis, Thomas W. Glover

Journal:

Year:

1995

Language:

english

File:

PDF, 144 KB

english, 1995

25

Description and genetic mapping ofPolypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations

Jessica A. Lehoczky, Wei-Wen Cai, Julie A. Douglas, Jennifer L. Moran, David R. Beier, Jeffrey W. Innis

Journal:

Mammalian Genome

Year:

2006

Language:

english

File:

PDF, 350 KB

english, 2006

26

Evolution of N-terminal sequences of the vertebrate HOXA13 protein

Douglas P. Mortlock, Praveen Sateesh, Jeffrey W. Innis

Journal:

Mammalian Genome

Year:

2000

Language:

english

File:

PDF, 810 KB

english, 2000

27

BMP4loss-of-function mutations in developmental eye disorders including SHORT syndrome

Linda M. Reis, Rebecca C. Tyler, Kala F. Schilter, Omar Abdul-Rahman, Jeffrey W. Innis, Beth A. Kozel, Adele S. Schneider, Tanya M. Bardakjian, Edward J. Lose, Donna M. Martin, Ulrich Broeckel, Elena

Journal:

Year:

2011

Language:

english

File:

PDF, 1.96 MB

english, 2011

28

A mouse transgene drives embryonic dorsal posterior commissure expression

Jessica A. Lehoczky, Jeffrey W. Innis

Journal:

Transgenic Research

Year:

2007

Language:

english

File:

PDF, 262 KB

english, 2007

29

Developmental Biology: Frontiers for Clinical Genetics: Limb development: molecular dysmorphology is at hand!

Jeffrey W Innis, Douglas P Mortlock

Journal:

Clinical Genetics

Year:

1998

Language:

english

File:

PDF, 5.72 MB

english, 1998

30

Conserved expression domains for genes upstream and within the HoxA and HoxD clusters suggests a long-range enhancer existed before cluster duplication

Jessica A. Lehoczky, Melissa E. Williams, Jeffrey W. Innis

Journal:

Evolution & Development

Year:

2004

Language:

english

File:

PDF, 1.90 MB

english, 2004

31

Expanded HOXA13 polyalanine tracts in a monotreme

Jessica A. Lehoczky, Jeffrey W. Innis

Journal:

Evolution & Development

Year:

2008

Language:

english

File:

PDF, 238 KB

english, 2008

32

BAC transgenic analysis reveals enhancers sufficient for Hoxa13 and neighborhood gene expression in mouse embryonic distal limbs and genital bud

Jessica A. Lehoczky, Jeffrey W. Innis

Journal:

Evolution & Development

Year:

2008

Language:

english

File:

PDF, 3.31 MB

english, 2008

33

10.1038/36234

Kondo, Takashi, Zákány, József, Innis, Jeffrey W., Duboule, Denis

Journal:

Year:

1997

Language:

english

File:

PDF, 217 KB

english, 1997

34

The molecular basis of hypodactyly (Hd): a deletion in Hoxa13 leads to arrest of digital arch formation

Mortlock, Douglas P., Post, Laura C., Innis, Jeffrey W.

Journal:

Nature Genetics

Year:

1996

File:

PDF, 942 KB

1996

35

Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation

Matthew G. Butler, Susan L. Dagenais, José L. Garcia-Perez, Pascal Brouillard, Miikka Vikkula, Peter Strouse, Jeffrey W. Innis, Thomas W. Glover

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 768 KB

english, 2012

36

Haploinsufficiency of SF3B4, a Component of the Pre-mRNA Spliceosomal Complex, Causes Nager Syndrome

Francois P. Bernier, Oana Caluseriu, Sarah Ng, Jeremy Schwartzentruber, Kati J. Buckingham, A. Micheil Innes, Ethylin Wang Jabs, Jeffrey W. Innis, Jane L. Schuette, Jerome L. Gorski, Peter H. Byers, G

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 639 KB

english, 2012

37

Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings

Shane C. Quinonez, Peter Hedera, Mason Barr, Todd Ackley, Cindy Lam, Anjali Purkayastha, Thomas W. Glover, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 265 KB

english, 2012

38

Severe Limb Defects in Hypodactyly Mice Result from the Expression of a Novel, Mutant HOXA13 Protein

Laura C Post, Elliott H Margulies, Anne Kuo, Jeffrey W Innis

Journal:

Developmental Biology

Year:

2000

Language:

english

File:

PDF, 450 KB

english, 2000

39

Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome

Wisam Al Badr, Suha Al Bader, Edgar Otto, Friedhelm Hildebrandt, Todd Ackley, Weiping Peng, Jishu Xu, Jun Li, Kailey M. Owens, David Bloom, Jeffrey W. Innis

Journal:

Journal of Pediatric Urology

Year:

2011

Language:

english

File:

PDF, 545 KB

english, 2011

40

R172: Normative Soft Palate Dimensions: Correlation to Sleep Apnea

William Innis, Jeffrey H. Spiegel, Osamu Sakai

Journal:

Otolaryngology - Head and Neck Surgery

Year:

2007

Language:

english

File:

PDF, 35 KB

english, 2007

41

Range of HOX/TALE superclass associations and protein domain requirements for HOXA13:MEIS interaction

Thomas M. Williams, Melissa E. Williams, Jeffrey W. Innis

Journal:

Developmental Biology

Year:

2005

Language:

english

File:

PDF, 752 KB

english, 2005

42

Candidate downstream regulated genes of HOX group 13 transcription factors with and without monomeric DNA binding capability

Thomas M. Williams, Melissa E. Williams, Rork Kuick, David Misek, Kevin McDonagh, Samir Hanash, Jeffrey W. Innis

Journal:

Developmental Biology

Year:

2005

Language:

english

File:

PDF, 727 KB

english, 2005

43

Long-range regulation of Hoxa13 in limb development

Jessica A. Lehoczky, Melissa E. Williams, Jeffrey W. Innis

Journal:

Developmental Biology

Year:

2006

Language:

english

File:

PDF, 64 KB

english, 2006

44

A group 13 homeodomain is neither necessary nor sufficient for posterior prevalence in the mouse limb

Melissa E. Williams, Jessica A. Lehoczky, Jeffrey W. Innis

Journal:

Developmental Biology

Year:

2006

Language:

english

File:

PDF, 751 KB

english, 2006

45

Phenotypic heterogeneity in the presentation of d-2-hydroxyglutaric aciduria in monozygotic twins

Vinod K. Misra, Eduard A. Struys, William O’Brien, Gajja S. Salomons, Thomas Glover, Cornelis Jakobs, Jeffrey W. Innis

Journal:

Molecular Genetics and Metabolism

Year:

2005

Language:

english

File:

PDF, 132 KB

english, 2005

46

Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome

Frances R. Goodman, Chiara Bacchelli, Angela F. Brady, Louise A. Brueton, Jean-Pierre Fryns, Douglas P. Mortlock, Jeffrey W. Innis, Lewis B. Holmes, Alan E. Donnenfeld, Murray Feingold, Frits A. Beeme

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 312 KB

english, 2000

47

A Novel Frameshift Mutation in Exon 23 of ATP7A (MNK) Results in Occipital Horn Syndrome and Not in Menkes Disease

Susan L. Dagenais, Ayla N. Adam, Jeffrey W. Innis, Thomas W. Glover

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 580 KB

english, 2001

48

Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia

William A. Paznekas, Simeon A. Boyadjiev, Robert E. Shapiro, Otto Daniels, Bernd Wollnik, Catherine E. Keegan, Jeffrey W. Innis, Mary Beth Dinulos, Cathy Christian, Mark C. Hannibal, Ethylin Wang Jabs

Journal:

The American Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 530 KB

english, 2003

49

High affinity dopamine D2 receptor radioligands. 2. [125I]epidepride, a potent and specific radioligand for the characterization of striatal and extrastriatal dopamine D2 receptors

Robert M. Kessler, M. Sib Ansari, Dennis E. Schmidt, Tomas de Paulis, Jeffrey A. Clanton, Roberts Innis, Mohammed Al-Tikriti, Ronald G. Manning, David Gillespie

Journal:

Year:

1991

Language:

english

File:

PDF, 995 KB

english, 1991

50

Peripheral Cannabinoid-1 Receptor Inverse Agonism Reduces Obesity by Reversing Leptin Resistance

Joseph Tam, Resat Cinar, Jie Liu, Grzegorz Godlewski, Daniel Wesley, Tony Jourdan, Gergő Szanda, Bani Mukhopadhyay, Lee Chedester, Jeih-San Liow, Robert B. Innis, Kejun Cheng, Kenner C. Rice, Jeffrey

Journal:

Cell Metabolism

Year:

2012

Language:

english

File:

PDF, 865 KB

english, 2012