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Julia Richards

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Yi Lu; Stuart Macgregor; David A Mackey; Alex MacLeod; Nicholas G Martin; Richard A Mills; Alireza Mirshahi; Paul Mitchell; Grant W Montgomery; Sayoko E Moroi; Jenny Mountain; Ayse B Ozel; Chi P Pang; Louis R Pasquale; Craig Pennell; Norbert Pfeiffer; Ozren Polasek; Yaron S Rabinowitz; Wishal D Ramdas; Julia E Richards; Jerome I Rotter; Igor Rudan; Seang Mei Saw; David Siscovick; Timothy D Spector; Henriët Springelkamp; Kari Stefansson; E Shyong Tai; Wan-Ting Tay; Kent D Taylor; Clement C Y Tham; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Megan Ulmer; Cornelia M van Duijn; Zoran Vatavuk; Virginie J M Verhoeven; Ananth C Viswanathan; Veronique Vitart; Eranga N Vithana; Jie Jin Wang; Janey L Wiggs; Colin Willoughby; James F Wilson; Roger Wolfs; R Rand Allingham; Michael G Anderson; Wei Ang; Allison Ashley-Koch; Tin Aung; Kathryn P Burdon; Yelena Bykhovskaya; Harry Campbell; Raphaële Castagne; Li J Chen; Ching-Yu Cheng; Belinda K Cornes; Jamie E Craig; Angela J Cree; David P Dimasi; Sarah Ennis; Brian Fleck; Jia-Nee Foo; Jane Gibson; Franz Grus; Jonathan L Haines; Christopher J Hammond; Michael A Hauser; Caroline Hayward; Alex W Hewitt; René Hoehn; Pirro G Hysi; Fridbert Jonasson; Jae H Kang; Chiea Chuen Khor; Caroline C W Klaver; Demelza Koehn; Karl J Lackner; Dexter Y L Leung; Jun Li; Xiaohui Li; Jianjun Liu; Andrew J Lotery; Alan F Wright; Jian Yang; Brian L Yaspan; Seyhan Yazar; Terri L Young; Tanja Zeller; Tien Y Wong
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
Louis R Pasquale; Margaret A Pericak-Vance; Tony Realini; Douglas J Rhee; Julia E Richards; Joel S Schuman; Kuldev Singh; Douglas Vollrath; Robert N Weinreb; Gadi Wollstein; Brian L Yaspan; Donald J Zack; Kang Zhang; Wael Abdrabou; R Rand Allingham; Donald L Budenz; Teresa C Chen; Elizabeth Delbono; David S Friedman; Douglas Gaasterland; Terry Gaasterland; Cynthia L Grosskreutz; Jonathan L Haines; Michael A Hauser; Jae H Kang; Richard K Lee; Paul R Lichter; Yutao Liu; Stephanie J Loomis; Catherine A McCarty; Sayoko E Moroi; Lana M Olson; Janey L Wiggs
CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States.
Dong Shi; Ai Shimizu; Yoshimasa Takano; Kotaro Yamamoto; Noriko Yasuda; Haruki Abe; Takeo Fukuchi; Tomoyo Funayama; Hidenao Ideta; Yukihiko Mashima; MinGe Mengkegale; Akiko Miyazawa; Toru Nakazawa; Kohji Nishida; Julia E Richards; Nobuo Fuse
Association of HK2 and NCK2 with normal tension glaucoma in the Japanese population.

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All Publications

2013: Yi Lu; Stuart Macgregor; David A Mackey; Alex MacLeod; Nicholas G Martin; Richard A Mills; Alireza Mirshahi; Paul Mitchell; Grant W Montgomery; Sayoko E Moroi; Jenny Mountain; Ayse B Ozel; Chi P Pang; Louis R Pasquale; Craig Pennell; Norbert Pfeiffer; Ozren Polasek; Yaron S Rabinowitz; Wishal D Ramdas; Julia E Richards; Jerome I Rotter; Igor Rudan; Seang Mei Saw; David Siscovick; Timothy D Spector; Henriët Springelkamp; Kari Stefansson; E Shyong Tai; Wan-Ting Tay; Kent D Taylor; Clement C Y Tham; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Megan Ulmer; Cornelia M van Duijn; Zoran Vatavuk; Virginie J M Verhoeven; Ananth C Viswanathan; Veronique Vitart; Eranga N Vithana; Jie Jin Wang; Janey L Wiggs; Colin Willoughby; James F Wilson; Roger Wolfs; R Rand Allingham; Michael G Anderson; Wei Ang; Allison Ashley-Koch; Tin Aung; Kathryn P Burdon; Yelena Bykhovskaya; Harry Campbell; Raphaële Castagne; Li J Chen; Ching-Yu Cheng; Belinda K Cornes; Jamie E Craig; Angela J Cree; David P Dimasi; Sarah Ennis; Brian Fleck; Jia-Nee Foo; Jane Gibson; Franz Grus; Jonathan L Haines; Christopher J Hammond; Michael A Hauser; Caroline Hayward; Alex W Hewitt; René Hoehn; Pirro G Hysi; Fridbert Jonasson; Jae H Kang; Chiea Chuen Khor; Caroline C W Klaver; Demelza Koehn; Karl J Lackner; Dexter Y L Leung; Jun Li; Xiaohui Li; Jianjun Liu; Andrew J Lotery; Alan F Wright; Jian Yang; Brian L Yaspan; Seyhan Yazar; Terri L Young; Tanja Zeller; Tien Y Wong
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
Nature genetics 2013;45(2):155-63.
2013: Louis R Pasquale; Margaret A Pericak-Vance; Tony Realini; Douglas J Rhee; Julia E Richards; Joel S Schuman; Kuldev Singh; Douglas Vollrath; Robert N Weinreb; Gadi Wollstein; Brian L Yaspan; Donald J Zack; Kang Zhang; Wael Abdrabou; R Rand Allingham; Donald L Budenz; Teresa C Chen; Elizabeth Delbono; David S Friedman; Douglas Gaasterland; Terry Gaasterland; Cynthia L Grosskreutz; Jonathan L Haines; Michael A Hauser; Jae H Kang; Richard K Lee; Paul R Lichter; Yutao Liu; Stephanie J Loomis; Catherine A McCarty; Sayoko E Moroi; Lana M Olson; Janey L Wiggs
CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States.
American journal of ophthalmology 2013;155(2):342-353.e5.
2013: Dong Shi; Ai Shimizu; Yoshimasa Takano; Kotaro Yamamoto; Noriko Yasuda; Haruki Abe; Takeo Fukuchi; Tomoyo Funayama; Hidenao Ideta; Yukihiko Mashima; MinGe Mengkegale; Akiko Miyazawa; Toru Nakazawa; Kohji Nishida; Julia E Richards; Nobuo Fuse
Association of HK2 and NCK2 with normal tension glaucoma in the Japanese population.
PloS one 2013;8(1):e54115.
2012: Joshua D Stein; Nidhi Talwar; Bin Nan; Paula Anne Newman-Casey; Julia E Richards; David C Musch
The relationship between statin use and open-angle glaucoma.
Ophthalmology 2012;119(10):2074-81.
2012: Megan Ulmer; Douglas Vollrath; Robert Weinreb; Janey L Wiggs; Gadi Wollstein; Brian L Yaspan; Terri Young; Donald J Zack; Kang Zhang; Felicia Hawthorne; Jae H Kang; Richard Lee; Jun Li; Paul R Lichter; Yutao Liu; Sayoko E Moroi; Ayse Bilge Ozel; Louis R Pasquale; Margaret Pericak-Vance; Anthony Realini; Julia E Richards; Joel Schuman; Kuldev Singh; R Rand Allingham; Allison Ashley-Koch; Donald L Budenz; David S Friedman; Douglas Gaasterland; Jonathan Haines; Michael A Hauser
Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia.
Investigative ophthalmology & visual science 2012;53(8):4468-74.
2012: Veronica Mendoza-Reinoso; Teja S Patil; Rodolfo Perez-Grossmann; Julia E Richards; Enrique Vargas; Wilder Castillo-Herrera; Silvia Fernández; Maria L Guevara-Fujita; Frank Lizaraso-Caparó; Ricardo Fujita
Novel and known MYOC exon 3 mutations in an admixed Peruvian primary open-angle glaucoma population.
Molecular vision 2012;18():2067-75.
2012: Janey L Wiggs; Gadi Wollstein; Brian L Yaspan; Sachiko Yoneyama; Donald J Zack; Kang Zhang; Wael Abdrabou; R Rand Allingham; Wendy Brodeur; Donald L Budenz; Joseph Caprioli; Andrew Thomas Crenshaw; Kristy Crooks; Elizabeth Delbono; Kimberly F Doheny; Jason Ernst; Bao J Fan; David S Friedman; Douglas Gaasterland; Terry Gaasterland; Michael A Hauser; Jae H Kang; Manolis Kellis; Cathy Laurie; Richard Lee; Paul R Lichter; Yutao Liu; Stephanie Loomis; Tomohiro Masuda; Cathy McCarty; Felipe A Medeiros; Daniel Mirel; Sayoko E Moroi; David C Musch; Lana M Olson; Louis R Pasquale; Margaret Pericak-Vance; Anthony Realini; Julia E Richards; Frank W Rozsa; Joel Schuman; Kathleen Scott; Kuldev Singh; Joshua D Stein; Edward H Trager; Paul Vanveldhuisen; Douglas Vollrath; Dan Y Wang; Robert N Weinreb; Jonathan L Haines
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS genetics 2012;8(4):e1002654.
2011: Linda Zhang; Mark W Johnson; Julia E Richards; Yang Sun; Sayoko E Moroi
Combined cilioretinal artery and central vein occlusions in juvenile glaucoma.
Archives of ophthalmology 2011;129(9):1231-4.
2011: Joshua D Stein; Nidhi Talwar; Janey L Wiggs; Jae Hee Kang; Denise S Kim; Bin Nan; Louis R Pasquale; David M Reed; Julia E Richards
Geographic and climatic factors associated with exfoliation syndrome.
Archives of ophthalmology 2011;129(8):1053-60.
2011: Joshua D Stein; Denise S Kim; Leslie M Niziol; Nidhi Talwar; Bin Nan; David C Musch; Julia E Richards
Differences in rates of glaucoma among Asian Americans and other racial groups, and among various Asian ethnic groups.
Ophthalmology 2011;118(6):1031-7.
2011: Yutao Liu; Sayoko E Moroi; Julia E Richards; Cecile M Santiago-Turla; Joshua Wheeler; Leon W Herndon; Lydia Coulter Kwee; Paul R Lichter; Stephen K Akafo; R Rand Allingham; Donald L Budenz; Pratap Challa; Douglas E Gaasterland; Jason Gibson; Christopher A Girkin; Michael A Hauser
GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease.
PloS one 2011;6(11):e27134.
2008: Maria-Luisa Guevara-Fujita; Rodolfo A Perez-Grossmann; Alejandro Estrada-Cuzcano; Hemant Pawar; Enrique Vargas; Julia E Richards; Ricardo Fujita
Recurrent Myocilin Asn480Lys glaucoma causative mutation arises de novo in a family of Andean descent.
Journal of glaucoma 2008;17(1):67-72.
2008: Frank W Rozsa; Kathleen Scott; Hemant Pawar; Sayoko E Moroi; Julia E Richards
Effects of timolol on MYOC, OPTN, and WDR36 RNA levels.
Archives of ophthalmology 2008;126(1):86-93.
2007: Anthony J Aldave; V Yellore; Fei Yu; Nirit Bourla; Baris Sonmez; Andrew K Salem; Sylvia A Rayner; Kapil M Sampat; Charles M Krafchak; Julia E Richards
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.
American journal of medical genetics. Part A 2007;143A(21):2549-56.
2007: Edward H Trager; Ritu Khanna; Adrian Marrs; Lawrence Siden; Kari E H Branham; Anand Swaroop; Julia E Richards
Madeline 2.0 PDE: a new program for local and web-based pedigree drawing.
Bioinformatics (Oxford, England) 2007;23(14):1854-6.
2007: Katy Downs; David N Zacks; Rafael Caruso; Athanasios J Karoukis; Kari E H Branham; Beverly M Yashar; Mark H Haimann; Karmen M Trzupek; Meira Meltzer; Delphine Blain; Julia E Richards; Richard G Weleber; John R Heckenlively; Paul Sieving; Radha Ayyagari
Molecular testing for hereditary retinal disease as part of clinical care.
Archives of ophthalmology 2007;125(2):252-8.
2007: Alex W Hewitt; John R Samples; R Rand Allingham; Irma Järvelä; Georgios Kitsos; Subbaiah Ramasamy Krishnadas; Julia E Richards; Paul R Lichter; Michael B Petersen; Sundaresan Periasamy; Janey L Wiggs; David A Mackey; Mary K Wirtz
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds.
Molecular vision 2007;13():487-92.
2007: Rosa M Ayala-Lugo; Hemant Pawar; David Reed; Paul R Lichter; Sayoko E Moroi; Michael Page; James Eadie; Veronica Azocar; Eugenio A Maul; Christine Ntim-Amponsah; William Bromley; Ebenezer Obeng-Nyarkoh; A Tim Johnson; Theresa Guckian Kijek; Catherine A Downs; Jenae M Johnson; Rodolfo A Perez-Grossmann; Maria-Luisa Guevara-Fujita; Ricardo Fujita; Margaret R Wallace; Julia E Richards
Variation in optineurin (OPTN) allele frequencies between and within populations.
Molecular vision 2007;13():151-63.
2007: Frank W Rozsa; Kathleen M Scott; Hemant Pawar; John R Samples; Mary K Wirtz; Julia E Richards
Differential expression profile prioritization of positional candidate glaucoma genes: the GLC1C locus.
Archives of ophthalmology 2007;125(1):117-27.
2007: Ning C McLaren; David Reed; David C Musch; Catherine A Downs; Misao E Higashi; Cecilia Santiago; Pauline A Radenbaugh; R Rand Allingham; Julia E Richards; Sayoko E Moroi
Evaluation of the beta2-adrenergic receptor gene as a candidate glaucoma gene in 2 ancestral populations.
Archives of ophthalmology 2007;125(1):105-11.
2007: Alex W Hewitt; Sonya L Bennett; Julia E Richards; David P Dimasi; Adam P Booth; Chris F Inglehearn; Rashida Anwar; Tetsuya Yamamoto; John H Fingert; Elise Héon; Jamie E Craig; David A Mackey
Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals.
Archives of ophthalmology 2007;125(1):98-104.
2006: Z Mimiwati; David A Mackey; Jamie E Craig; J R Mackinnon; Julian L Rait; J E Liebelt; R Ayala-Lugo; Douglas Vollrath; Julia E Richards
Nail-patella syndrome and its association with glaucoma: a review of eight families.
The British journal of ophthalmology 2006;90(12):1505-9.
2006: Pauline A Radenbaugh; Anju Goyal; Ning C McLaren; David Reed; David C Musch; Julia E Richards; Sayoko E Moroi
Concordance of aqueous humor flow in the morning and at night in normal humans.
Investigative ophthalmology & visual science 2006;47(11):4860-4.
2006: Abigail Woodroffe; Charles M Krafchak; Nobuo Fuse; Paul R Lichter; Sayoko E Moroi; Robert M Schertzer; Catherine A Downs; William L Duren; Michael Boehnke; Julia E Richards
Ordered subset analysis supports a glaucoma locus at GLC1I on chromosome 15 in families with earlier adult age at diagnosis.
Experimental eye research 2006;82(6):1068-74.
2006: Frank W Rozsa; David Reed; Kathleen M Scott; Hemant Pawar; Sayoko E Moroi; Theresa Guckian Kijek; Charles M Krafchak; Mohammad I Othman; Douglas Vollrath; Victor M Elner; Julia E Richards
Gene expression profile of human trabecular meshwork cells in response to long-term dexamethasone exposure.
Molecular vision 2006;12():125-41.
2005: Charles M Krafchak; Hemant Pawar; Sayoko E Moroi; Alan Sugar; Paul R Lichter; David A Mackey; Shahzad I Mian; Theresa M Cooney; Victor M Elner; Miriam T Schteingart; Catherine A Downs; Theresa Guckian Kijek; Jenae M Johnson; Edward H Trager; Frank W Rozsa; Md Nawajes A Mandal; Michael P Epstein; Douglas Vollrath; Radha Ayyagari; Michael Boehnke; Julia E Richards
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
American journal of human genetics 2005;77(5):694-708.
2005: Sepideh Zareparsi; Monika Buraczynska; Kari E H Branham; Sapna Shah; Donna Eng; Mingyao Li; Hemant Pawar; Beverly M Yashar; Sayoko E Moroi; Paul R Lichter; Howard R Petty; Julia E Richards; Goncalo Abecasis; Victor M Elner; Anand Swaroop
Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration.
Human molecular genetics 2005;14(11):1449-55.
2005: Rodney S Bucher; Edward F Hall; David Reed; Julia E Richards; Mark W Johnson; David N Zacks
Effect of intravitreal triamcinolone acetonide on susceptibility to experimental bacterial endophthalmitis and subsequent response to treatment.
Archives of ophthalmology 2005;123(5):649-53.
2004: Satoko Shimizu; Charles M Krafchak; Nobuo Fuse; Michael P Epstein; Miriam T Schteingart; Alan Sugar; Maya Eibschitz-Tsimhoni; Catherine A Downs; Frank W Rozsa; Edward H Trager; David Reed; Michael Boehnke; Sayoko E Moroi; Julia E Richards
A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.
American journal of medical genetics. Part A 2004;130A(4):372-7.
2004: Leonard A Levin; Robert Ritch; Julia E Richards; Teresa Borrás
Stem cell therapy for ocular disorders.
Archives of ophthalmology 2004;122(4):621-7.
2004: Brian P Brooks; Sayoko E Moroi; Catherine A Downs; Shannon Wiltse; Mohammad I Othman; Elena V Semina; Julia E Richards
A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome.
Ophthalmic genetics 2004;25(1):57-62.
2004: Goncalo Abecasis; Beverly M Yashar; Yu Zhao; Noor M Ghiasvand; Sepideh Zareparsi; Kari E H Branham; Adam C Reddick; Edward H Trager; Shigeo Yoshida; John Bahling; Elena Filippova; Susan G Elner; Mark W Johnson; Andrew K Vine; Paul Sieving; Samuel G Jacobson; Julia E Richards; Anand Swaroop
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease.
American journal of human genetics 2004;74(3):482-94.
2003: Pauline Lim; Paul R Lichter; Misao Higashi; Catherine A Downs; Julia E Richards
Septuagenarian's phenotype leads to ascertainment of familial MYOC gene mutation.
Journal of glaucoma 2003;12(2):98-103.
2003: Sayoko E Moroi; Parag A Gokhale; Miriam T Schteingart; Alan Sugar; Catherine A Downs; Satoko Shimizu; Charles M Krafchak; Nobuo Fuse; Susan G Elner; Victor M Elner; Andrew Flint; Michael P Epstein; Michael Boehnke; Julia E Richards
Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy.
American journal of ophthalmology 2003;135(4):461-70.
2002: Radha Ayyagari; F Yesim Demirci; Jiafan Liu; Eve L Bingham; Heather M Stringham; Laura E Kakuk; Michael Boehnke; Michael B Gorin; Julia E Richards; Paul Sieving
X-linked recessive atrophic macular degeneration from RPGR mutation.
Genomics 2002;80(2):166-71.
2002: Debra A Thompson; Christina L McHenry; Yun Li; Julia E Richards; Mohammad I Othman; Eberhard Schwinger; Douglas Vollrath; Samuel G Jacobson; Andreas Gal
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively.
American journal of human genetics 2002;70(1):224-9.
2001: Julia E Richards; Robert Ritch
The seventh annual Optic Nerve Rescue And Regeneration Think Tank: Immune modulation and gene expression in glaucoma.
Journal of glaucoma 2001;10(4):361-3.
2001: Julia E Richards; R Ritch
The sixth annual Optic Nerve Rescue and Regeneration Think Tank: developmental genetics in glaucoma.
Journal of glaucoma 2001;10(1):71-3.
2000: Debra A Thompson; P Gyürüs; L L Fleischer; Eve L Bingham; Christina L McHenry; E Apfelstedt-Sylla; E Zrenner; B Lorenz; Julia E Richards; Samuel G Jacobson; Paul Sieving; Andreas Gal
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
Investigative ophthalmology & visual science 2000;41(13):4293-9.
2000: Satoko Shimizu; Paul R Lichter; A Tim Johnson; Z Zhou; Misao Higashi; MS Gottfredsdottir; Mohammad I Othman; Sayoko E Moroi; Frank W Rozsa; Robert M Schertzer; M S Clarke; A L Schwartz; Catherine A Downs; Douglas Vollrath; Julia E Richards
Age-dependent prevalence of mutations at the GLC1A locus in primary open-angle glaucoma.
American journal of ophthalmology 2000;130(2):165-77.
1999: Frances A Farley; Paul R Lichter; Catherine A Downs; Iain McIntosh; Douglas Vollrath; Julia E Richards
An orthopaedic scoring system for nail-patella syndrome and application to a kindred with variable expressivity and glaucoma.
Journal of pediatric orthopedics 1999;19(5):624-31.
1999: C C Zimmerman; Vishwanath R Lingappa; Julia E Richards; Frank W Rozsa; Paul R Lichter; Jon R Polansky
A trabecular meshwork glucocorticoid response (TIGR) gene mutation affects translocational processing.
Molecular vision 1999;5():19.
1999: Paul Sieving; Eve L Bingham; J Kemp; Julia E Richards; Kelaginamane T Hiriyanna
Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave.
American journal of ophthalmology 1999;128(2):179-84.
1999: Kelaginamane T Hiriyanna; Eve L Bingham; Beverly M Yashar; Radha Ayyagari; Gerald A Fishman; Kent W Small; David V Weinberg; Richard G Weleber; R A Lewis; sten andreasson; Julia E Richards; Paul Sieving
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.
Human mutation 1999;14(5):423-7.
1998: Mohammad I Othman; S A Sullivan; G L Skuta; D A Cockrell; Heather M Stringham; Catherine A Downs; A Fornés; A Mick; Michael Boehnke; Douglas Vollrath; Julia E Richards
Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11.
American journal of human genetics 1998;63(5):1411-8.
1998: Frank W Rozsa; Satoko Shimizu; Paul R Lichter; A Tim Johnson; Mohammad I Othman; K Scott; Catherine A Downs; T D Nguyen; Jon R Polansky; Julia E Richards
GLC1A mutations point to regions of potential functional importance on the TIGR/MYOC protein.
Molecular vision 1998;4():20.
1998: W M Eyaid; MV Clough; H Root; Kathleen M Scott; MK McCormick; X Zhang; N A Lisitsyn; W G Kearns; Clair A Francomano; Julia E Richards; Iain McIntosh
Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs.
Human genetics 1998;103(4):525-6.
1998: Julia E Richards; Robert Ritch; Paul R Lichter; Frank W Rozsa; Heather M Stringham; R M Caronia; D Johnson; G P Abundo; J Willcockson; Catherine A Downs; Debra A Thompson; Maria A Musarella; N Gupta; Mohammad I Othman; D M Torrez; S B Herman; D J Wong; Misao Higashi; Michael Boehnke
Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
Ophthalmology 1998;105(9):1698-707.
1998: Douglas Vollrath; VL Jaramillo-Babb; MV Clough; Iain McIntosh; Kathleen M Scott; Paul R Lichter; Julia E Richards
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome.
Human molecular genetics 1998;7(7):1091-8.
1997: Cathleen M Lutz; Julia E Richards; K L Scott; S Sinha; T L Yang-Feng; Wayne N Frankel; Debra A Thompson
Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YY.
Genomics 1997;46(2):287-90.
1997: Qais A Farjo; A Jackson; S Pieke-Dahl; K Scott; William J Kimberling; Paul Sieving; Julia E Richards; Anand Swaroop
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration.
Genomics 1997;45(2):395-401.
1997: Paul R Lichter; Julia E Richards; Catherine A Downs; Heather M Stringham; Michael Boehnke; Frances A Farley
Cosegregation of open-angle glaucoma and the nail-patella syndrome.
American journal of ophthalmology 1997;124(4):506-15.
1997: Cathleen M Lutz; Wayne N Frankel; Julia E Richards; Debra A Thompson
Neuropeptide Y receptor genes on human chromosome 4q31-q32 map to conserved linkage groups on mouse chromosomes 3 and 8.
Genomics 1997;41(3):498-500.
1997: Paul R Lichter; Julia E Richards; Michael Boehnke; Mohammad I Othman; B D Cameron; Heather M Stringham; Catherine A Downs; S B Lewis; B F Boyd
Juvenile glaucoma linked to the GLC1A gene on chromosome 1q in a Panamanian family.
American journal of ophthalmology 1997;123(3):413-6.
1996: H Pawar; Eve L Bingham; Kelaginamane T Hiriyanna; M Segal; Julia E Richards; Paul Sieving
X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC.
Human heredity 1996;46(6):329-35.
1996: Y C Hou; Julia E Richards; Eve L Bingham; H Pawar; K Scott; M Segal; Kathryn L Lunetta; Michael Boehnke; Paul Sieving
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.
Human heredity 1996;46(4):211-20.
1996: Julia E Richards; Paul R Lichter; S Herman; E R Hauser; Y C Hou; A T Johnson; Michael Boehnke
Probable exclusion of GLC1A as a candidate glaucoma gene in a family with middle-age-onset primary open-angle glaucoma.
Ophthalmology 1996;103(7):1035-40.
1996: A T Johnson; Julia E Richards; Michael Boehnke; Heather M Stringham; S B Herman; D J Wong; Paul R Lichter
Clinical phenotype of juvenile-onset primary open-angle glaucoma linked to chromosome 1q.
Ophthalmology 1996;103(5):808-14.
1996: B F Koop; Julia E Richards; T D Durfee; J Bansberg; J Wells; Anita Gilliam; H L Chen; A Clausell; P W Tucker; Frederick R Blattner
Analysis and comparison of the mouse and human immunoglobulin heavy chain JH-Cmu-Cdelta locus.
Molecular phylogenetics and evolution 1996;5(1):33-49.
1996: Paul R Lichter; Julia E Richards; Michael Boehnke; Mohammad I Othman; B D Cameron; Heather M Stringham; Catherine A Downs; S B Lewis; B F Boyd
Juvenile glaucoma linked to GLCIA in a Panamanian family.
Transactions of the American Ophthalmological Society 1996;94():335-46; discussion 347-51.
1995: H Pawar; Eve L Bingham; Kathryn L Lunetta; M Segal; Julia E Richards; Michael Boehnke; Paul Sieving
Refined genetic mapping of juvenile X-linked retinoschisis.
Human heredity 1995;45(4):206-10.
1995: Julia E Richards; Kathleen M Scott; Paul Sieving
Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa.
Ophthalmology 1995;102(4):669-77.
1995: A Nicoletti; D J Wong; K Kawase; L H Gibson; TL Yang-Feng; Julia E Richards; Debra A Thompson
Molecular characterization of the human gene encoding an abundant 61 kDa protein specific to the retinal pigment epithelium.
Human molecular genetics 1995;4(4):641-9.
1995: Paul Sieving; Julia E Richards; F Naarendorp; Eve L Bingham; K Scott; M Alpern
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(3):880-4.
1994: Denise Yan; D Wong; K Zheng; D Thiselton; R Fujita; Paul Sieving; S S Bhattacharya; TL Yang-Feng; Julia E Richards; Anand Swaroop
Dinucleotide repeat polymorphism at the DXS977 locus.
Human molecular genetics 1994;3(6):1030.
1994: Julia E Richards; Paul R Lichter; Michael Boehnke; J L Uro; D Torrez; D Wong; A T Johnson
Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome Iq.
American journal of human genetics 1994;54(1):62-70.
1991: Julia E Richards; C Y Kuo; Michael Boehnke; Paul Sieving
Rhodopsin Thr58Arg mutation in a family with autosomal dominant retinitis pigmentosa.
Ophthalmology 1991;98(12):1797-805.
1990: A J Hanzlik; M Binder; W M Layton; L Rowe; M Layton; B A Taylor; M M Osemlak; Julia E Richards; David M Kurnit; G D Stewart
The murine situs inversus viscerum (iv) gene responsible for visceral asymmetry is linked tightly to the Igh-C cluster on chromosome 12.
Genomics 1990;7(3):389-93.
1988: Julia E Richards; T C Gilliam; J L Cole; Mitchell L Drumm; JJ Wasmuth; James Gusella; Francis S Collins
Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(17):6437-41.
1984: Anita Gilliam; A Shen; Julia E Richards; Frederick R Blattner; J F Mushinski; P W Tucker
Illegitimate recombination generates a class switch from C mu to C delta in an IgD-secreting plasmacytoma.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(13):4164-8.
1983: Julia E Richards; Anita Gilliam; A Shen; P W Tucker; Frederick R Blattner
Unusual sequences in the murine immunoglobulin mu-delta heavy-chain region.
Nature 1983;306(5942):483-7.
1982: P W Tucker; H L Cheng; Julia E Richards; L Fitzmaurice; J F Mushinski; Frederick R Blattner
Genetic aspects of IgD expression: III. Functional implications of the sequence and organization of the C delta gene.
Annals of the New York Academy of Sciences 1982;399():26-38.
1982: Frederick R Blattner; Julia E Richards; A Shen; M Knapp; S Strober; Anita Gilliam; S Jones; H L Cheng; J F Mushinski; P W Tucker
Genetic aspects of IgD expression: I. Analysis of the Cmu-C delta complex in committed and uncommitted DNA.
Annals of the New York Academy of Sciences 1982;399():1-14.
1980: N Newell; Julia E Richards; P W Tucker; F R Blattner
J genes for heavy chain immunoglobulins of mouse.
Science (New York, N.Y.) 1980;209(4461):1128-32.
1979: P W Tucker; K B Marcu; N Newell; Julia E Richards; F R Blattner
Sequence of the cloned gene for the constant region of murine gamma 2b immunoglobulin heavy chain.
Science (New York, N.Y.) 1979;206(4424):1303-6.
1978: Oliver Smithies; A E Blechl; K Denniston-Thompson; N Newell; Julia E Richards; Jerry L Slightom; P W Tucker; F R Blattner
Cloning human fetal gamma globin and mouse alpha-type globin DNA: characterization and partial sequencing.
Science (New York, N.Y.) 1978;202(4374):1284-9.
1978: F R Blattner; A E Blechl; K Denniston-Thompson; H E Faber; Julia E Richards; Jerry L Slightom; P W Tucker; Oliver Smithies
Cloning human fetal gamma globin and mouse alpha-type globin DNA: preparation and screening of shotgun collections.
Science (New York, N.Y.) 1978;202(4374):1279-84.

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