Authors:
LENCER R
NOLTE A
KRECKER K
SCHWINGER E
AROLT V
Citation: R. Lencer et al., EYE TRACKING DYSFUNCTION (ETD) AS A MEASURABLE INDICATOR FOR THE VULNERABILITY TO SCHIZOPHRENIA, Schizophrenia research, 29(1-2), 1998, pp. 116-116
Authors:
AROLT V
LENCER R
SCHURMANN M
PURMANN S
KRECKER K
SCHWINGER E
Citation: V. Arolt et al., LINKAGE OF EYE TRACKING DYSFUNCTION TO DNA-MARKERS ON CHROMOSOME 6P21IN SCHIZOPHRENIA, Schizophrenia research, 29(1-2), 1998, pp. 138-139
Authors:
AROLT V
TEICHERT HM
STEEGE D
LENCER R
HEIDE W
Citation: V. Arolt et al., DISTINGUISHING SCHIZOPHRENIC-PATIENTS FROM HEALTHY CONTROLS BY QUANTITATIVE MEASUREMENT OF EYE-MOVEMENT PARAMETERS, Biological psychiatry, 44(6), 1998, pp. 448-458
Authors:
LENCER R
AROTT V
PURMANN S
SCHURMANN M
MULLERMYHSOK B
NOLTE A
KRECKER K
SCHWINGER E
Citation: R. Lencer et al., LINKAGE ANALYSES OF EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q, American journal of medical genetics, 74(6), 1997, pp. 595-595
Citation: K. Krecker et al., DEFICITS OF EYE-MOVEMENTS IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA AND NORMAL-FAMILIES - PERFORMANCE IN A REFLEXIVE SACCADIC TASK, American journal of medical genetics, 74(6), 1997, pp. 598-598
Authors:
LENCER R
AROLT V
PURMANN S
SCHURMANN M
MULLERMYHSOK B
NOLTE A
KRECKER K
SCHWINGER E
Citation: R. Lencer et al., LINKAGE ANALYSES OF EYE-TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q, American journal of medical genetics, 74(6), 1997, pp. 666-666
Authors:
AROLT V
LENCER R
NOLTE A
PINNOW M
SCHWINGER E
Citation: V. Arolt et al., EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA, European archives of psychiatry and clinical neuroscience, 246(4), 1996, pp. 175-181
Authors:
AROLT V
LENCER R
NOLTE A
MULLERMYHSOK B
PURMANN S
SCHURMANN M
LEUTELT J
PINNOW M
SCHWINGER E
Citation: V. Arolt et al., EYE TRACKING DYSFUNCTION IS A PUTATIVE PHENOTYPIC SUSCEPTIBILITY MARKER OF SCHIZOPHRENIA AND MAPS TO A LOCUS ON CHROMOSOME 6P IN FAMILIES WITH MULTIPLE OCCURRENCE OF THE DISEASE, American journal of medical genetics, 67(6), 1996, pp. 564-579