W. Kimberling

C. Cremers, W. Kimberling, R. Pennings, 2003, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese

W. Kimberling, S. Usami, S. Abe, 2001, Journal of Human Genetics.

Breast cancer,genetics, andageatfirst pregnancy

W. Kimberling, H. Lynch, J. Lynch, 1984 .

A common ancestral origin of the frequent and widespread 2299delG USH2A mutation.

C. Cremers, C. Möller, T. Rosenberg, 2001, American journal of human genetics.

Dyslexia subtypes: genetics, behavior, and brain imaging.

B. Pennington, H. Lubs, W. Kimberling, 1988, Research publications - Association for Research in Nervous and Mental Disease.

Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.

F. Hecht, W. Kimberling, 1971, American journal of human genetics.

Phenotypic variation in the familial atypical multiple mole-melanoma syndrome (FAMMM).

W. Kimberling, H. Lynch, J. Lynch, 1983, Journal of medical genetics.

Clinical and Genetic Heterogeneity of Usher Syndrome

W. Kimberling, 2003 .

Defective myosin VIIA gene responsible for Usher syndrome type IB

Steve D. M. Brown, K. Steel, A. Munnich, 1995, Nature.

Hearing impairment in Usher's syndrome.

C. Cremers, W. Kimberling, R. Pennings, 2002, Advances in oto-rhino-laryngology.

Histopathologic features of the temporal bone in usher syndrome type I.

C. Cremers, J. Nadol, W. Kimberling, 2000, Archives of otolaryngology--head & neck surgery.

Hearing impairment related to age in Usher syndrome types 1B and 2A.

C. Cremers, W. Kimberling, P. Huygen, 1999, Archives of otolaryngology--head & neck surgery.

Molecular Genetics of Hearing Disorders

W. Kimberling, 1998 .

Identification of three novel mutations in human EYA1 protein associated with branchio‐oto‐renal syndrome

C. Cremers, B. Schaefer, W. Kimberling, 1998, Human mutation.

Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12.

J. W. Askew, W. Kimberling, S. Smith, 1999, Genomics.

Familial Heterogeneity of Breast Cancer Risk

W. Kimberling, H. Lynch, J. Lynch, 1986 .

Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation.

W. Kimberling, P. M. Kelley, S. Usami, 2001, American journal of medical genetics.

Chromosomal abnormalities ascertained in the collaborative perinatal survey of 7- and 8-year-old children.

F. Hecht, N. Myrianthopoulos, W. Kimberling, 1979, Birth defects original article series.

Usher syndrome: An otoneurologic study

C. Möller, W. Kimberling, P. Brookhouser, 1989, The Laryngoscope.

The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41.

E. Zabarovsky, G. Klein, W. Kimberling, 1996, Genomics.

Segregation analysis of hereditary nonpolyposis colorectal cancer

R. Elston, D. Rao, J. Bailey-Wilson, 1986, Genetic epidemiology.

Development of a genotyping microarray for Usher syndrome

C. Cremers, M. Bitner-Glindzicz, E. van Wijk, 2006, Journal of Medical Genetics.

Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease.

Ann M. Johnson, P. Gabow, W. D. Kaehny, 1992 .

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

G. Richardson, W. Kimberling, P. Heyning, 1998, Nature Genetics.

Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.

C. Cremers, W. Kimberling, Shrawan Kumar, 2000, American journal of human genetics.

Double aneuploidy: the frequency of XXY in males with Down's syndrome.

F. Hecht, W. Kimberling, J. Miller, 1969, American journal of human genetics.

Longterm visual prognosis in Usher syndrome types 1 and 2.

C. Möller, W. Kimberling, A. Sjöström, 2006, Acta ophthalmologica Scandinavica.

A review of hereditary malignant melanoma including biomarkers in familial atypical multiple mole melanoma syndrome.

W. Kimberling, H. Lynch, J. Lynch, 1983, Cancer genetics and cytogenetics.

Linkage and gene localization of hereditary spherocytosis (HS).

Randolph K. Taylor, W. Kimberling, W. Kimberling, 1978, Blood.

Semen Analysis in the Usher Syndrome Type 2A

C. Cremers, W. Kimberling, M. Wagenaar, 1999, ORL.

Left-handedness and immune disorders in familial dyslexics.

M. Haith, B. Pennington, W. Kimberling, 1987, Archives of neurology.

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.

P. Sieving, A. Jackson, A. Swaroop, 1997, Genomics.

HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice

Allen C. Simpson, W. Kimberling, K. Avraham, 2015, PLoS genetics.

Genetic studies in a black family with autosomal dominant polycystic kidney disease and sickle-cell trait.

P. Gabow, W. Kimberling, A. Johnson, 1996, Nephron.

Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.

S. Leal, D. Stephan, M. Schiller, 2011, American journal of human genetics.

Familial dyslexia: use of genetic linkage data to define subtypes.

B. Pennington, W. Kimberling, S. Smith, 1990, Journal of the American Academy of Child and Adolescent Psychiatry.

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

H. Rehm, C. Cremers, C. Möller, 1998, Science.

Searching for evidence of DFNB2.

J. W. Askew, W. Kimberling, M. D. Weston, 2002, American journal of medical genetics.

Genetic Linkage Studies of Hereditary Hearing Loss

W. Kimberling, 2000 .

Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the Pendred gene.

W. Kimberling, S. Usami, S. Abe, 1999, American journal of medical genetics.

Exogenous progestogen and estrogen implicated in birth defects.

W. Kimberling, J. Nora, A. Nora, 1978, JAMA.

Hearing loss disorders associated with renal disease.

W. Kimberling, Richard J. H. Smith, N. Borsa, 2011, Advances in oto-rhino-laryngology.

Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.

D. Stephan, L. Tarantino, T. Wiltshire, 2009, American journal of human genetics.

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

J. W. Askew, D. Harris, W. Kimberling, 1998, American journal of human genetics.

Variable Clinical Features in Patients with CDH23 Mutations (USH1D-DFNB12)

C. Cremers, A. Deutman, H. Kremer, 2004, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies

R. Elston, M. Lipkin, J. Bailey-Wilson, 1985, Cancer.

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

J. W. Askew, W. Reardon, H. Kremer, 2002, American journal of human genetics.

Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium.

C. Möller, C. Berlin, B. Keats, 1994, American journal of medical genetics.

Duplication-deficiency of the short arm of chromosome 8 following artificial insemination.

H. Lubs, W. Kimberling, R. Weleber, 1976, Annales de genetique.

Familial bladder cancer in an oncology clinic.

W. Kimberling, H. Lynch, J. Lynch, 1987, Cancer genetics and cytogenetics.

Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I

E. Aller, W. Kimberling, A. Oshima, 2008, Human mutation.

Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.

W. Kimberling, M. Babu, Arun Kumar, 2004, Molecular vision.

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.

C. Möller, W. Kimberling, M. D. Weston, 2004, American journal of human genetics.

Identification of the mouse and rat orthologs of the gene mutated in Usher syndrome type IIA and the cellular source of USH2A mRNA in retina, a target tissue of the disease.

Jack R. Davis, Ming Zhou, W. Kimberling, 2002, Genomics.

Spectrum of mutations in USH2A in British patients with Usher syndrome type II.

A. Bird, S. Bhattacharya, W. Kimberling, 2001, Experimental eye research.

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

S. Jacobson, C. Cremers, W. Reardon, 2000, American journal of human genetics.

Clinical and molecular genetics of Usher syndrome.

C. Möller, W. Kimberling, 1995, Journal of the American Academy of Audiology.

Localization of two genes for Usher syndrome type I to chromosome 11.

W. Reardon, M. Jay, S. Daiger, 1992, Genomics.

Advancing genetic testing for deafness with genomic technology

Adam P. DeLuca, Christina M. Sloan, T. Casavant, 2013, Journal of Medical Genetics.

Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa

J. McGee, E. Walsh, W. Kimberling, 1997, Hearing Research.

Quantitative trait locus for reading disability on chromosome 6.

D W Fulker, L R Cardon, L. Cardon, 1994, Science.

Linkage and Selection Analysis of Biochemical Variants in Peromyscus maniculatus

W. Kimberling, J. Joule, R. Baccus, 1980 .

Alteration of Rod and Cone Function in Children with Usher Syndrome

C. Möller, W. Kimberling, E. Stone, 2011, European journal of ophthalmology.

Linkage of a gene causing high bone mass to human chromosome 11 (11q12-13)

Mark L. Johnson, R. Recker, W. Kimberling, 1997, American journal of human genetics.

Prevalent connexin 26 gene (GJB2) mutations in Japanese

W. Kimberling, P. M. Kelley, S. Usami, 2000, Journal of medical genetics.

HOMER 2 , a Stereociliary Scaffolding Protein , Is Essential for Normal Hearing in Humans and Mice

Allen C. Simpson, W. Kimberling, Richard J. H. Smith, 2017 .

Carrier detection in classical hemophilia.

W. Kimberling, W. Hathaway, M. Lubs, 1976, Pediatrics.

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis.

M. Pembrey, S. Daiger, M. Wagner, 1994, American journal of medical genetics.

Approaches to Understanding the Molecular Genetics of Hearing and Deafness

K. Steel, W. Kimberling, 1996 .

Early childhood hearing loss: Clinical and molecular genetics. An educational slide set of the American College of Medical Genetics

H. Rehm, K. Arnos, B. Korf, 2003, Genetics in Medicine.

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

G. B. Schaefer, D. Harris, W. Kimberling, 1999, Pediatrics.

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

S. Leal, A. Starr, B. Keats, 2003, Journal of medical genetics.

Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children

E. Stone, W. Kimberling, R. Weleber, 2010, Genetics in Medicine.

A New Clinical Classification for Usher's Syndrome Based on a New Subtype of Usher's Syndrome Type I

A Blankenagel, W. Kimberling, A. Blankenagel, 2001, The Laryngoscope.

Localization of Usher syndrome type II to chromosome 1q.

C. Möller, Y. Shugart, W. Kimberling, 1990, Genomics.

Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome.

Friedhelm Hildebrandt, Christine Petit, C. Petit, 2007, American journal of human genetics.

Phenotypic manifestations of branchiootorenal syndrome

M. Pembrey, C. Cremers, Yutaka Sato, 1995 .

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

B J Keats, L J Hood, C I Berlin, 2005, Journal of Medical Genetics.

Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing.

C. Cremers, W. Kimberling, Shrawan Kumar, 1997, Genetic testing.

Natural history of hereditary cancer of the breast and colon

W. Kimberling, H. Lynch, J. Lynch, 1982, Cancer.

A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa

C. Cremers, C. Möller, H. Kremer, 2016, Hearing Research.

Gene linkage and genetic deafness.

K. Steel, C. Cremers, H. Brunner, 1995, International journal of pediatric otorhinolaryngology.

Molecular Cloning and Domain Structure of Human Myosin-VIIa , the Gene Product Defective in Usher Syndrome 1 B

D. Corey, W. Kimberling, M. Ramakrishnan, 1996 .

EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family

W. Kimberling, Shrawan Kumar, S. Usami, 1999, Journal of Human Genetics.

Phenotypic manifestations of branchio-oto-renal syndrome.

M. Pembrey, C. Cremers, Y. Sato, 1995, American journal of medical genetics.

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

W. Kimberling, Shrawan Kumar, S. Tinley, 1992, Genomics.

Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium.

M. Leppert, B. Keats, W. Kimberling, 1992, Genomics.

Genetics and Otolaryngology

W. Kimberling, 2010 .

Clinical variability and genetic heterogeneity within the Acadian Usher population.

S. Daiger, B. Keats, W. Kimberling, 1992, American journal of medical genetics.

Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.

Y. Shugart, P. Gabow, W. Kimberling, 1990, Journal of medical genetics.

Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41.

W. Kimberling, M. Ma-Edmonds, M. D. Weston, 1998, Genomics.

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.

W. Reardon, P. Beighton, C. Möller, 1992, Genomics.

Multiple regression analysis of sib-pair data on reading to detect quantitative trait loci

L. Cardon, B. Pennington, D. Fulker, 1991 .

Specific reading disability: identification of an inherited form through linkage analysis.

B. Pennington, W. Kimberling, S. Smith, 1983, Science.

Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population

D. Stephan, J. Webster, M. Bahlo, 2010, The Annals of otology, rhinology, and laryngology.

A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family

D. Stephan, J. Webster, M. Bahlo, 2009, American journal of medical genetics. Part A.

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

A. J. Roman, K. Steel, T. Aleman, 2008, Human molecular genetics.

Usher syndromes due to MYO 7 A , PCDH 15 , USH 2 A or GPR 98 mutations share retinal disease mechanism

A. J. Roman, K. Steel, T. Aleman, 2008 .

Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss

D. Stephan, J. Webster, M. Bahlo, 2009, The Laryngoscope.

Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.

D. Corey, W. Kimberling, M. Ramakrishnan, 1996, Genomics.

Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.

C. Cremers, W. Kimberling, R. Ramesar, 2000, American journal of human genetics.

Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype.

A. J. Roman, T. Aleman, A. Cideciyan, 2005, Investigative ophthalmology & visual science.

Genetic linkage studies of autosomal dominant polycystic kidney disease: search for the second gene in a large Sicilian family

P. Gabow, W. Kimberling, Shrawan Kumar, 1991, Human Genetics.

Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

A. J. Roman, T. Aleman, A. Cideciyan, 2011, Investigative ophthalmology & visual science.

Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome

C. Möller, W. Kimberling, V. Ponjavic, 2011, Ophthalmic genetics.

ORIGINAL INVESTIGATIONS Pathogenesis and Treatment of Kidney Disease Presence of De Novo Mutations in Autosomal Dominant Polycystic Kidney Disease Patients Without Family History

Ann M. Johnson, P. Gabow, W. Kimberling, 2008 .

NATURAL COURSE OF VISUAL FIELD LOSS IN PATIENTS WITH TYPE 2 USHER SYNDROME

R. Massof, G. Fishman, W. Kimberling, 2007, Retina.

Volumetric neuroimaging in Usher syndrome: evidence of global involvement.

J. Bodensteiner, G. B. Schaefer, J. Thompson, 1998, American journal of medical genetics.

Report on Attempts to Localize Usher Syndrome Type 1 by Linkage Analysis to Selected Candidate Regions

Y. Shugart, W. Kimberling, M. D. Weston, 1991, Annals of the New York Academy of Sciences.

Genetic Studies of Usher Syndrome

Y. Shugart, W. Kimberling, M. D. Weston, 1991, Annals of the New York Academy of Sciences.

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family

W. Kimberling, S. Riazuddin, P. Söderkvist, 2009, European Journal of Human Genetics.

Clinical findings in obligate carriers of type I Usher syndrome.

C. Cremers, W. Kimberling, P. Huygen, 1995, American journal of medical genetics.

Quantitative trait locus for reading disability: correction.

D W Fulker, L R Cardon, L. Cardon, 1995, Science.

Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.

C. Cremers, C. Möller, W. Kimberling, 1995, American journal of human genetics.

Reassignment of a cancer family syndrome gene to chromosome 18.

W. Kimberling, B. Boman, H. Lynch, 1988, Cancer genetics and cytogenetics.

Serum IgM in retinitis pigmentosa: A genetic study

W. Kimberling, R. Spiro, R. Weleber, 1978, Clinical genetics.

Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q

C. Cremers, C. Möller, W. Kimberling, 2000, Journal of medical genetics.

Human NDUFB9 Gene: Genomic Organization and a Possible Candidate Gene Associated with Deafness Disorder Mapped to Chromosome 8q13

W. Kimberling, Shrawan Kumar, D. Wells, 1999, Human Heredity.

The prevalence of Usher Syndrome in Sweden: a nationwide epidemiological and clinical survey

C. Möller, W. Kimberling, M. Sadeghi, 2004 .

Analysis of a large pedigree with elliptocytosis, multiple lipomatosis, and biological false-positive serological test for syphilis.

M. Skolnick, W. Kimberling, J. Weinberg, 1980, American journal of medical genetics.

Usherin expression is highly conserved in mouse and human tissues

Joe C. Adams, W. Kimberling, N. Pearsall, 2002, Hearing Research.

Audiological and vestibular features in affected subjects with USH3: A genotype/phenotype correlation

C. Möller, W. Kimberling, M. Sadeghi, 2005, International journal of audiology.

Estimation of the frequency of occult mutations for an autosomal recessive disease in the presence of genetic heterogeneity: application to genetic hearing loss disorders

W. Kimberling, 2005, Human mutation.

Genetic and Clinical Features of Sensorineural Hearing Loss Associated With the 1555 Mitochondrial Mutation

W. Kimberling, S. Usami, S. Abe, 1997, The Laryngoscope.

The inheritance of psoriasis.

R. Dobson, W. Kimberling, 1980, The Journal of investigative dermatology.

Connexin 26: required for normal auditory function

W. Kimberling, P. M. Kelley, E. Cohn, 2000, Brain Research Reviews.

Spelling errors in adults with a form of familial dyslexia.

H A Lubs, B. Pennington, H. Lubs, 1986, Child development.

For the Record: The History of Precursors to Malignant Melanoma-Reply

W. Kimberling, H. Lynch, R. Fusaro, 1984 .

Familial atypical multiple mole melanoma syndrome (FAMMM)

W. Kimberling, H. Lynch, R. Fusaro, 1983, Archives of Dermatology.

Heterogeneity of Usher Syndrome Type I

A. Bird, M. Jay, W. Kimberling, 1993 .

Expressivity of hearing loss in cases with Usher syndrome type IIA

C. Möller, W. Kimberling, E. Cohn, 2013, International journal of audiology.

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

W. Kimberling, S. Horai, S. Usami, 1998, European Journal of Human Genetics.

Is hearing loss due to mutations in the Connexin 26 gene progressive?

W. Jesteadt, W. Kimberling, P. M. Kelley, 2008, International journal of audiology.

Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.

W. Kimberling, S. Usami, S. Abe, 1998, Journal of communication disorders.

Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.

A. J. Roman, T. Aleman, A. Cideciyan, 2009, Investigative ophthalmology & visual science.

Kinetics of visual field loss in Usher syndrome Type II.

G. Somes, W. Kimberling, S. Kritchevsky, 2004, Investigative ophthalmology & visual science.

Localization and expression of usherin: a novel basement membrane protein defective in people with Usher’s syndrome type IIa

W. Kimberling, Caroline Miller, M. Jablonski, 2002, Hearing Research.

Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations.

Jack R. Davis, S. Jacobson, C. Möller, 2002, American journal of human genetics.

Racial differences in the frequency of Q and C chromosomal heteromorphisms

S. Patil, W. Kimberling, R. Summitt, 1977, Nature.

The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).

D. Corey, W. Kimberling, T. Hasson, 1997, Genomics.

Genetic heterogeneity of Usher syndrome.

W. Kimberling, D. Orten, S. Pieke-Dahl, 2000, Advances in oto-rhino-laryngology.

Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family

C. Cremers, A. Deutman, H. Kremer, 2003, Human Genetics.

Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32.

W. Kimberling, M. Ma-Edmonds, M. D. Weston, 1997, Genomics.

Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.

A. J. Roman, T. Aleman, A. Cideciyan, 2008, Investigative ophthalmology & visual science.

A new highly polymorphic dinucleotide (CT)n repeat polymorphism D1S158 on chromosome 1q isolated by microdissection.

W. Kimberling, M. D. Weston, L. Overbeck, 1992, Human Molecular Genetics.

Genetic–Epidemiologic Study of Early–onset Ischemic Heart Disease

W. Kimberling, J. Nora, A. Nora, 1980, Circulation.

Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I

I. MacDonald, W. Kimberling, O. Lehmann, 2012, Molecular vision.

A novel mutation in COCH—implications for genotype‐phenotype correlations in DFNA9 hearing loss

D. Stephan, J. Webster, M. Bahlo, 2010, The Laryngoscope.

Genetic heterogeneity of Usher syndrome type II in a Dutch population.

C. Cremers, W. Kimberling, A. Dobin, 1996, Journal of medical genetics.

USH2A Mutation analysis in 70 Dutch families with Usher syndrome type II

C. Cremers, A. Deutman, H. Kremer, 2004, Human mutation.

Identification of novel USH2A mutations: implications for the structure of USH2A protein

T. Rosenberg, W. Kimberling, M. D. Weston, 2000, European Journal of Human Genetics.

Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome

W. Kimberling, H. Ayadi, D. Orten, 2002, Journal of medical genetics.

Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center

W. Sanger, G. B. Schaefer, W. Kimberling, 1993, Human mutation.

Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR).

D. Porteous, K. Evans, W. Kimberling, 1993, Human molecular genetics.

Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.

C. Cremers, W. Kimberling, Shrawan Kumar, 1992, Human molecular genetics.

Screening for multiple genes influencing dyslexia

B. Pennington, W. Kimberling, Shelley D. Smith, 1991 .

Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13.

C. Cremers, W. Kimberling, H. Marres, 1998, American journal of medical genetics.

Audiological findings in Usher syndrome types IIa and II (non-IIa)

C. Möller, W. Kimberling, M. Sadeghi, 2004, International journal of audiology.

An Introduction to the Genetics of Normal and Defective Hearing a

W. Kimberling, M. Mazzoli, A. Martini, 1997, Annals of the New York Academy of Sciences.

Medical genetics, Huntington's chorea, and legal questions pertaining to autopsy.

W. Kimberling, H. Lynch, P. Lynch, 1983, The American journal of medicine.

[From gene to disease; genetic causes of hearing loss and visual impairment sometimes accompanied by vestibular problems (Usher syndrome)].

C. Cremers, A. Deutman, H. Kremer, 2002, Nederlands tijdschrift voor geneeskunde.

Genetic heterogeneity of Usher syndrome type II.

J. Furman, C. Möller, W. Kimberling, 1993, Journal of medical genetics.

Pharmacogenetic application of methods from population genetics

W. Kimberling, D. Goldgar, M. Penno, 1987, Clinical pharmacology and therapeutics.

Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.

C. Cremers, B. Oostra, J. Darby, 1994, The New England journal of medicine.

Identification of three novel mutations in human EYA1 protein associated with branchio‐oto‐renal syndrome

C. Cremers, B. Schaefer, W. Kimberling, 1998, Human mutation.

A twin methodology for the study of genetic and environmental control of variation in human smoking behavior.

J. S. Williams, S. G. Vandenberg, G. Mcclearn, 1979, Acta geneticae medicae et gemellologiae.

Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.

W. Kimberling, M. Mazaheri, S. Diehl, 1999, Journal of craniofacial genetics and developmental biology.

Hereditary deafness

W. Kimberling, 1898, American journal of medical genetics.

Autosomal dominant polycystic kidney disease: localization of the second gene to chromosome 4q13-q23.

P. Gabow, W. Kimberling, S. Somlo, 1993, Genomics.

Linkage heterogeneity of autosomal dominant polycystic kidney disease.

P. Gabow, W. Kimberling, P. Fain, 1988, The New England journal of medicine.

Familial heterogeneity of colon cancer risk

W. Kimberling, H. Lynch, J. Lynch, 1986, Cancer.

Developmental Continuities and Discontinuities in a Form of Familial Dyslexia

B. Pennington, H. Lubs, W. Kimberling, 1984 .

Segregation analysis of autosomal dominant polycystic kidney disease

Y. Shugart, P. Gabow, W. Kimberling, 1993, Genetic epidemiology.

Genetics and smoking‐associated cancers. A study of 485 families

W. Kimberling, H. Lynch, J. Lynch, 1986, Cancer.

Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

A. J. Roman, T. Aleman, A. Cideciyan, 2011, Investigative ophthalmology & visual science.

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

J. Heckenlively, W. Kimberling, M. D. Weston, 2000, American journal of human genetics.

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

A. Starr, C. Berlin, W. Kimberling, 2005, Journal of Medical Genetics.

Hearing Loss in Usher Syndrome Type II is Nonprogressive

W. Kimberling, C. Reisser, C. Otterstedde, 2002, The Annals of otology, rhinology, and laryngology.

Genetic predisposition to breast cancer

W. Kimberling, A. Spreadborough, H. Lynch, 1984, Cancer.

Chromosomal Localization of the Heterochromatic Region 16qh(.76) linked to α-Haptoglobin in Man

F. Hecht, W. Kimberling, R. Magenis, 1971, Nature.