J.H.A.M. Tuerlings - Concepedia

Author

J.H.A.M. Tuerlings

Also Known As

J H A M Tuerlings, J H Tuerlings, J Tuerlings, J. H. A. M. TUERLINGS, J. H. A. M. Tuerlings, J. H. Tuerlings, J. H.A.M. Tuerlings, J. TUERLINGS, J. Tuerlings, J.H.A.M Tuerlings

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center University of Groningen University of Amsterdam Rijnstate Hospital

About

J.H.A.M. Tuerlings is an author at Radboud University Nijmegen specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	17	721
2	Public Health	8	8	358
3	Biology	1	1	43
4	Biostatistics	1	1	22
5	Clinical Sciences	1	1	38

J.H.A.M. Tuerlings

Publications

Citations

H-Index

Page 1

	Year	Citations
Microdeletions of the Y chromosome and intracytoplasmic sperm injection: from gene to clinic Jan A.M. Kremer, J.H.A.M. Tuerlings, E J Meuleman, Human Reproduction FertilityGeneticsReproductive HealthGynecologyIntracytoplasmic Sperm Injection	1997	117
Reproductive decisions of men with microdeletions of the Y chromosome: the role of genetic counselling Annemiek Nap, Ron J.T. Van Golde, J.H.A.M. Tuerlings, Human Reproduction Counselling ProcessFamily MedicineFertilityGeneticsReproductive Health	1999	107
Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27 Hans van Bokhoven, Martin Jung, Arie P.T. Smits, The American Journal of Human Genetics Developmental AnomalyThumb HypoplasiaDevelopmental BiologyMendelian DisorderLimb Mammary Syndrome	1999	105
Localization of the gene for X-linked Alport's syndrome Han G. Brunner, C.H. Schröder, Cor van Bennekom, Kidney International X-linked AlportMendelian DisorderGenetic DisorderGeneticsHistopathology	1988	80
Electroconvulsive Therapy for Catatonia Jeroen A. van Waarde, J.H.A.M. Tuerlings, B Verwey, Journal of Ect	2010	76
Trismus‐pseudocamptodactyly syndrome is caused by recurrent mutation of <i>MYH8</i> Reha M. Toydemir, Harold Chen, Virginia K. Proud, American Journal of Medical Genetics Part A	2006	74
Mutation Frequency of Cystic Fibrosis Transmembrane Regulator is not Increased in Oligozoospermic Male Candidates For Intracytoplasmic Sperm Injection J.H.A.M. Tuerlings, Bart Mol, Jan A.M. Kremer, Fertility and Sterility	1998	51
IS INCREASED CAG REPEAT LENGTH IN THE ANDROGEN RECEPTOR GENE A RISK FACTOR FOR MALE SUBFERTILITY? Ron van Golde, Kjeld van Houwelingen, Lambertus A. Kiemeney, The Journal of Urology	2002	45
A new locus for postaxial polydactyly type A/B on chromosome 7q21–q34 Robert‐Jan H. Galjaard, Arie P.T. Smits, J.H.A.M. Tuerlings, European Journal of Human Genetics BiologyCytogeneticsGenetic DisorderGeneticsNew Locus	2003	43
A retrospective study of 34 catatonic patients: analysis of clinical care and treatment J.H.A.M. Tuerlings, Jeroen A. van Waarde, B Verwey General Hospital Psychiatry Retrospective StudySleep DisordersSleepGeriatric PsychiatrySleep Health	2010	38

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